LMNA gene related symptoms and diseases
All the information presented here about the LMNA gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,ORPHANET,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to LMNA gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Congestive heart failure | Uncommon - Between 30% and 50% cases |
| Flexion contracture | Uncommon - Between 30% and 50% cases |
| Lipodystrophy | Uncommon - Between 30% and 50% cases |
| Hypertriglyceridemia | Uncommon - Between 30% and 50% cases |
| Myopathy | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with LMNA gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Arrhythmia
- Hypertension
- Skeletal muscle atrophy
- Insulin resistance
- Micrognathia
- Lipoatrophy
- Short stature
- Dilated cardiomyopathy
And 657 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to LMNA gene
Here you will find a list of rare diseases related to the LMNA. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
POLYCYSTIC OVARY SYNDROME 1; PCOS1
Alternate names
POLYCYSTIC OVARY SYNDROME 1; PCOS1 Is also known as pco, pco1, hyperandrogenemia, stein-leventhal syndrome, pcos
Description
a health problem that can affect a woman's menstrual cycle, fertility, hormones, insulin production, heart, blood vessels, and appearance
Most common symptoms of POLYCYSTIC OVARY SYNDROME 1; PCOS1
- Neoplasm
- Abnormality of metabolism/homeostasis
- Obesity
- Diabetes mellitus
- Apnea
More info about POLYCYSTIC OVARY SYNDROME 1; PCOS1
RESTRICTIVE DERMOPATHY
Alternate names
RESTRICTIVE DERMOPATHY Is also known as fetal hypokinesia sequence due to restrictive dermopathy, hyperkeratosis-contracture syndrome, lethal restrictive dermopathy, tight skin contracture syndrome, lethal, tight skin contracture syndrome
Description
Restrictive dermopathy (RD) is a neonatal lethal genetic disease characterized by very tight and thin skin with erosions and scaling, associated to a typical facial dysmorphism, arthrogryposis multiplex, fetal akinesia or hypokinesia deformation sequence (FADS) (see these terms) and pulmonary hypoplasia without neurological abnormalities.
Most common symptoms of RESTRICTIVE DERMOPATHY
- Growth delay
- Hypertelorism
- Micrognathia
- Abnormal facial shape
- Low-set ears
More info about RESTRICTIVE DERMOPATHY
FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE
Alternate names
FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE Is also known as fpl2, lipoatrophic diabetes, lipodystrophy, reverse partial, fpld2, familial partial lipodystrophy type 2, lipodystrophy, familial, of limbs and lower trunk, dunnigan syndrome, lipodystrophy, familial partial, dunnigan type
Description
Familial Partial lipodystrophy, Dunnigan type (FPLD2) is a rare form of genetic lipodystrophy (see this term) characterized by a loss of subcutaneous adipose tissue from the trunk, buttocks and limbs; fat accumulation in the neck, face, axillary and pelvic regions; muscular hypertrophy; and usually associated with metabolic complications such as insulin resistance, diabetes mellitus, dyslipidemia and liver steatosis.
Most common symptoms of FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE
- Short stature
- Micrognathia
- Cataract
- Hypertension
- Hepatomegaly
More info about FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE
FAMILIAL PARTIAL LIPODYSTROPHY, KÖBBERLING TYPE
Alternate names
FAMILIAL PARTIAL LIPODYSTROPHY, KÖBBERLING TYPE Is also known as fpld1, familial partial lipodystrophy type 1, lipodystrophy, familial partial, kobberling type
Description
Familial partial lipodystrophy, Köbberling type, is a very rare form of familial partial lipodystrophy (FPLD; see this term) of unknown etiology characterized by lipoatrophy that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes have also been associated. Inheritance is thought to be autosomal dominant.
Most common symptoms of FAMILIAL PARTIAL LIPODYSTROPHY, KÖBBERLING TYPE
- Hypertension
- Hepatomegaly
- Obesity
- Diabetes mellitus
- Hepatic steatosis
More info about FAMILIAL PARTIAL LIPODYSTROPHY, KÖBBERLING TYPE
AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY
Alternate names
AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY Is also known as scapuloilioperoneal atrophy with cardiopathy, emd2, muscular dystrophy, limb-girdle, type 1b, formerly, emery-dreifuss muscular dystrophy, autosomal dominant, edmd2, cardiomyopathy, dilated, with quadriceps myopathy, muscular dystrophy, proximal, type 1b, forme
Description
EDMD is characterized by myopathic changes in certain skeletal muscles and early contractures at the neck, elbows, and Achilles tendons, as well as cardiac conduction defects. 'Classic' Emery-Dreifuss muscular dystrophy (EDMD1 ) is an X-linked disorder caused by mutation in the emerin gene (EMD ) on Xq28 (Emery, 1989).For a discussion of genetic heterogeneity of EDMD, see {310300}.
Most common symptoms of AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY
- Intellectual disability
- Generalized hypotonia
- Scoliosis
- Muscle weakness
- Muscular hypotonia
More info about AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY
AUTOSOMAL RECESSIVE EMERY-DREIFUSS MUSCULAR DYSTROPHY
Alternate names
AUTOSOMAL RECESSIVE EMERY-DREIFUSS MUSCULAR DYSTROPHY Is also known as edmd3
Description
Emery-Dreifuss muscular dystrophy is characterized classically by the triad of weakness of the shoulder and pelvic girdle muscles, contractures of the elbows, neck, and Achilles tendon, and cardiac involvement, most commonly arrhythmias (summary by Jimenez-Escrig et al., 2012).For a discussion of genetic heterogeneity of EDMD, see {310300}.
Most common symptoms of AUTOSOMAL RECESSIVE EMERY-DREIFUSS MUSCULAR DYSTROPHY
- Intellectual disability
- Scoliosis
- Micrognathia
- Muscle weakness
- Abnormal facial shape
More info about AUTOSOMAL RECESSIVE EMERY-DREIFUSS MUSCULAR DYSTROPHY
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9; ARVD9
Alternate names
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9; ARVD9 Is also known as arvc9, arrhythmogenic right ventricular cardiomyopathy 9
Most common symptoms of ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9; ARVD9
- Congestive heart failure
- Dilatation
- Sudden cardiac death
- Syncope
- Palpitations
More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9; ARVD9
CHARCOT-MARIE-TOOTH DISEASE TYPE 2B1
Alternate names
CHARCOT-MARIE-TOOTH DISEASE TYPE 2B1 Is also known as ar-cmt2b1, charcot-marie-tooth disease, neuronal, type 2b1, charcot-marie-tooth neuropathy, type 2b1, autosomal recessive axonal cmt4c1, autosomal recessive charcot-marie-tooth disease type 2b1, charcot-marie-tooth disease, axonal, autosomal recessive, type 2b
Description
Charcot-Marie-Tooth disease, type 2B1 (CMT2B1, also referred to as CMT4C1) is an axonal CMT peripheral sensorimotor polyneuropathy.
Most common symptoms of CHARCOT-MARIE-TOOTH DISEASE TYPE 2B1
- Areflexia
- Hyporeflexia
- Pes cavus
- Kyphoscoliosis
- Proximal muscle weakness
More info about CHARCOT-MARIE-TOOTH DISEASE TYPE 2B1
AUTOSOMAL DOMINANT LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 1B
Alternate names
AUTOSOMAL DOMINANT LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 1B Is also known as lgmd1b, limb-girdle muscular dystrophy due to lamin a/c deficiency
Description
Autosomal dominant limb-girdle muscular dystrophy type 1B (LGMD1B) is a subtype of autosomal dominant limb girdle muscular dystrophy characterized by a variable age of onset of progressive shoulder and hip girdle weakness, with inferior limbs usually being affected prior to upper limbs, and mild joint contractures. LGMD1B is also associated with cardiac dysrhythmias, including atrioventricular conduction blocks, and late-onset dilated cardiomyopathy, that may lead to sudden death.
Most common symptoms of AUTOSOMAL DOMINANT LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 1B
- Seizures
- Generalized hypotonia
- Scoliosis
- Muscle weakness
- Flexion contracture
More info about AUTOSOMAL DOMINANT LIMB-GIRDLE MUSCULAR DYSTROPHY TYPE 1B
FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION
Alternate names
FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION Is also known as cardiomyopathy, familial idiopathic, cardiomyopathy, idiopathic dilated, cardiomyopathy, dilated, with conduction defect 1, cdcd1, cardiomyopathy, congestive
Description
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase.
Most common symptoms of FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION
- Ataxia
- Pain
- Fatigue
- Ventriculomegaly
- Cardiomyopathy
More info about FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT DUE TO LMNA MUTATION
CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION
Alternate names
CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION Is also known as mdcl, lmna-related congenital muscular dystrophy, l-cmd
Description
Congenital muscular dystrophy due to LMNA mutation is a rare congenital muscular dystrophy characterized by prominent axial hypotonia, dropped head syndrome, predominantly proximal muscle weakness in upper limbs/distal in lower limbs (with absent, poor or lost motor development), joint contractures (initially distal, later proximal), spine rigidity, and early respiratory insufficiency, in the presence of moderately elevated serum creatine kinase. Cardiac arrhythmias and sudden death have been also reported.
Most common symptoms of CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION
- Global developmental delay
- Generalized hypotonia
- Growth delay
- Failure to thrive
- Muscle weakness
More info about CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION
WERNER SYNDROME
Alternate names
WERNER SYNDROME Is also known as ws, adult progeria
Description
Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.
Most common symptoms of WERNER SYNDROME
- Short stature
- Neoplasm
- Pain
- Cataract
- Visual impairment
More info about WERNER SYNDROME
DILATED CARDIOMYOPATHY-HYPERGONADOTROPIC HYPOGONADISM SYNDROME
Alternate names
DILATED CARDIOMYOPATHY-HYPERGONADOTROPIC HYPOGONADISM SYNDROME Is also known as cardiomyopathy, dilated, with premature ovarian failure, genital anomaly with cardiomyopathy, najjar syndrome, cardiomyopathy, congestive, with hypergonadotropic hypogonadism, cardiogenital syndrome, cardiomyopathy with primary testicular failure, malouf syndro
Description
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH).
Most common symptoms of DILATED CARDIOMYOPATHY-HYPERGONADOTROPIC HYPOGONADISM SYNDROME
- Intellectual disability
- Short stature
- Scoliosis
- Cryptorchidism
- Ptosis
More info about DILATED CARDIOMYOPATHY-HYPERGONADOTROPIC HYPOGONADISM SYNDROME
MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY
Most common symptoms of MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY
- Short stature
- Hearing impairment
- Muscular hypotonia
- Cataract
- Flexion contracture
More info about MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY
SOURCES: ORPHANET
MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA
Alternate names
MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA Is also known as craniomandibular dermatodysostosis, lipodystrophy, type a, associated with mandibuloacral dysplasia
Description
Mandibuloacral dysplasia with type A lipodystrophy (MADA) is an autosomal recessive disorder characterized by growth retardation, craniofacial anomalies with mandibular hypoplasia, skeletal abnormalities with progressive osteolysis of the distal phalanges and clavicles, and pigmentary skin changes. The lipodystrophy is characterized by a marked acral loss of fatty tissue with normal or increased fatty tissue in the neck and trunk. Some patients may show progeroid features. Metabolic complications can arise due to insulin resistance and diabetes (Young et al., 1971; Simha and Garg, 2002; summary by Garavelli et al., 2009).See also MAD type B (MADB ), which is caused by mutation in the ZMPSTE24 gene (OMIM ).
Most common symptoms of MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA
- Short stature
- Generalized hypotonia
- Hearing impairment
- Growth delay
- Neoplasm
More info about MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA
SOURCES: OMIM
HUTCHINSON-GILFORD PROGERIA SYNDROME
Alternate names
HUTCHINSON-GILFORD PROGERIA SYNDROME Is also known as progeria, hgps
Description
Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat).
Most common symptoms of HUTCHINSON-GILFORD PROGERIA SYNDROME
- Intellectual disability
- Short stature
- Hearing impairment
- Scoliosis
- Growth delay
More info about HUTCHINSON-GILFORD PROGERIA SYNDROME
HEART-HAND SYNDROME, SLOVENIAN TYPE
Alternate names
HEART-HAND SYNDROME, SLOVENIAN TYPE Is also known as atriodigital dysplasia, slovenian type, cardiac conduction disease-dilated cardiomyopathy-brachydactyly syndrome
Description
Heart-hand syndrome of Slovenian type is a rare autosomal dominant form of heart-hand syndrome (see this term), first described in members of a Slovenian family, that is characterized by adult onset, progressive cardiac conduction disease, tachyarrhythmias that can lead to sudden death, dilated cardiomyopathy and brachydactyly, with the hands less severely affected than the feet. Muscle weakness and/or myopathic electromyographic findings have been observed in some cases.
Most common symptoms of HEART-HAND SYNDROME, SLOVENIAN TYPE
- Muscle weakness
- Flexion contracture
- Brachydactyly
- Cardiomyopathy
- Myopathy
More info about HEART-HAND SYNDROME, SLOVENIAN TYPE
LEFT VENTRICULAR NONCOMPACTION
Alternate names
LEFT VENTRICULAR NONCOMPACTION Is also known as spongy myocardium, lvnc, left ventricular hypertrabeculation, left ventricular noncompaction 1 with or without congenital heart defects
Description
Left ventricular noncompaction (LVNC) is a rare cardiomyopathy characterized anatomically by prominent left ventricular trabeculae and deep intratrabecular recesses causing progressive systolic and diastolic dysfunction, conduction abnormalities, and occasionally thromboembolic events.
Most common symptoms of LEFT VENTRICULAR NONCOMPACTION
- Abnormal facial shape
- Ventricular septal defect
- Respiratory distress
- Congestive heart failure
- Patent ductus arteriosus
More info about LEFT VENTRICULAR NONCOMPACTION
ATYPICAL WERNER SYNDROME
Alternate names
ATYPICAL WERNER SYNDROME Is also known as atypical progeroid syndrome
Description
Atypical Werner syndrome refers to a heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS; see this term) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, patients generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population.
Most common symptoms of ATYPICAL WERNER SYNDROME
- Short stature
- Failure to thrive
- Micrognathia
- Hypertension
- Skeletal muscle atrophy
More info about ATYPICAL WERNER SYNDROME
SOURCES: ORPHANET
AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY
Most common symptoms of AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY
- Micrognathia
- Hepatomegaly
- Myopathy
- Congestive heart failure
- Splenomegaly
More info about AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY
SOURCES: ORPHANET
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, LEFT DOMINANT FORM
Alternate names
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, LEFT DOMINANT FORM Is also known as familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form
More info about FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, LEFT DOMINANT FORM
SOURCES: ORPHANET
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, BIVENTRICULAR FORM
Alternate names
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, BIVENTRICULAR FORM Is also known as familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form
More info about FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, BIVENTRICULAR FORM
SOURCES: ORPHANET
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, RIGHT DOMINANT FORM
Alternate names
FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, RIGHT DOMINANT FORM Is also known as familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form, familial isolated arrhythmogenic ventricular dysplasia, classic form, familial isolated arrhythmogenic ventricular cardiomyopathy, classic form
More info about FAMILIAL ISOLATED ARRHYTHMOGENIC VENTRICULAR DYSPLASIA, RIGHT DOMINANT FORM
SOURCES: ORPHANET
LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME
Alternate names
LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME Is also known as lcps
Description
LMNA-related cardiocutaneous progeria syndrome is a rare, genetic, premature aging syndrome characterized by adulthood-onset cutaneous manifestations that result in a prematurely aged appearance (i.e. premature thinning and graying of scalp hair, loss of subcutaneous fat, tightening of skin) associated with prominent cardiovascular manifestations, such as accelerated atherosclerosis, calcific valve disease, and cardiomyopathy. Patients present loss of eyebrows and eyelashes in childhood and have a predisposition to develop malignancies.
Most common symptoms of LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME
- Hypertension
- Cardiomyopathy
- Congestive heart failure
- Sparse hair
- Ventricular hypertrophy
More info about LMNA-RELATED CARDIOCUTANEOUS PROGERIA SYNDROME
SOURCES: ORPHANET
Search interest in LMNA
Potential gene panels for LMNA gene
CMT Advanced Evaluation - Dominant, Axonal Panel
United States.
By Athena Diagnostics Inc CMT Advanced Evaluation - Dominant, Axonal that also includes the following genes: YARS MFN2 TRPV4 DNM2 HSPB8 GARS HSPB1 LMNA MPZ NEFL
More info about this panel United States.
CMT Advanced Evaluation - Comprehensive Panel
United States.
By Athena Diagnostics Inc CMT Advanced Evaluation - Comprehensive that also includes the following genes: YARS PRX GDAP1 LITAF FIG4 MFN2 TRPV4 FGD4 SBF2 SH3TC2
More info about this panel United States.
CMT Advanced Evaluation - Axonal Panel
United States.
By Athena Diagnostics Inc CMT Advanced Evaluation - Axonal that also includes the following genes: YARS GDAP1 MFN2 TRPV4 DNM2 HSPB8 GARS GJB1 HSPB1 LMNA
More info about this panel United States.
CMT Advanced Evaluation - Recessive Panel
United States.
By Athena Diagnostics Inc CMT Advanced Evaluation - Recessive that also includes the following genes: PRX GDAP1 FIG4 FGD4 SBF2 SH3TC2 LMNA MTMR2 NDRG1
More info about this panel United States.
LMNA (CMT2B1) DNA Sequencing Test Panel
United States.
By Athena Diagnostics Inc
This panel specifically test the LMNA gene.
More info about this panel United States.
Lamin A/C (LMNA) DNA Sequencing Test Panel
United States.
By Athena Diagnostics Inc
This panel specifically test the LMNA gene.
More info about this panel United States.
CMT Advanced Evaluation - Nonprevalent Panel
United States.
By Athena Diagnostics Inc CMT Advanced Evaluation - Nonprevalent that also includes the following genes: YARS PRX GDAP1 LITAF FIG4 TRPV4 FGD4 SBF2 SH3TC2 DNM2
More info about this panel United States.
Emery-Dreifuss Muscular Dystrophy Advanced Sequencing Evaluation Panel
United States.
By Athena Diagnostics Inc Emery-Dreifuss Muscular Dystrophy Advanced Sequencing Evaluation that also includes the following genes: SYNE2 SYNE1 TMEM43 EMD FHL1 LMNA
More info about this panel United States.
Limb Girdle Muscular Dystrophy Advanced Evaluation Panel
United States.
By Athena Diagnostics Inc Limb Girdle Muscular Dystrophy Advanced Evaluation that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Muscular Dystrophy Advanced Evaluation Panel
United States.
By Athena Diagnostics Inc Muscular Dystrophy Advanced Evaluation that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CCDC78 CAPN3 DNAJB6
More info about this panel United States.
Congenital Muscular Dystrophy Advanced Sequencing Evaluation Panel
United States.
By Athena Diagnostics Inc Congenital Muscular Dystrophy Advanced Sequencing Evaluation that also includes the following genes: TCAP RXYLT1 B4GAT1 SELENON FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2
More info about this panel United States.
CMT Advanced Evaluation - Nonprevalent Axonal Panel
United States.
By Athena Diagnostics Inc CMT Advanced Evaluation - Nonprevalent Axonal that also includes the following genes: YARS GDAP1 TRPV4 DNM2 HSPB8 GARS GJB1 HSPB1 LMNA NEFL
More info about this panel United States.
Charcot-Marie-Tooth Hereditary Neuropathy Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Charcot-Marie-Tooth Hereditary Neuropathy Panel that also includes the following genes: SBF1 SLC12A6 SPG11 SURF1 TFG VCP YARS PRX BSCL2 GDAP1
More info about this panel United States.
Comprehensive Cardiac Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Comprehensive Cardiac Panel that also includes the following genes: RIT1 RYR2 SCN1B SCN2B SCN4B SCN5A SGCD SLC22A5 BRAF SNTA1
More info about this panel United States.
Neuromuscular Disorders Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Neuromuscular Disorders Panel that also includes the following genes: RYR1 BIN1 SCN4A SGCA SGCB SGCD SGCE SGCG SLC25A4 SUCLA2
More info about this panel United States.
Dilated & Arrhythmogenic Cardiomyopathies Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Dilated & Arrhythmogenic Cardiomyopathies Panel that also includes the following genes: RYR2 SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TRDN
More info about this panel United States.
Congenital Contractures Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Congenital Contractures Panel that also includes the following genes: SKI SLC18A3 TNNI2 TNNT3 TPM2 TPM3 UBA1 ZMPSTE24 ACTA1 ADGRG6
More info about this panel United States.
Lamin A/C - LMNA Sequencing Panel
United States.
By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
This panel specifically test the LMNA gene.
More info about this panel United States.
Lamin A/C - LMNA Del/Dup Analysis Panel
United States.
By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
This panel specifically test the LMNA gene.
More info about this panel United States.
Dilated cardiomyopathy - full panel Panel
Canada.
By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario Dilated cardiomyopathy - full panel that also includes the following genes: SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL ACTC1
More info about this panel Canada.
Dilated cardiomyopathy - familial variant analysis Panel
Canada.
By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario Dilated cardiomyopathy - familial variant analysis that also includes the following genes: SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL ACTC1
More info about this panel Canada.
Pan-cardiomyopathy panel Panel
Canada.
By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario Pan-cardiomyopathy panel that also includes the following genes: RYR2 SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panel Canada.
Cardiomyopathy Panel Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Cardiomyopathy Panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SCO2 SGCD SKI BRAF SNTA1 SOS1
More info about this panel United States.
Dilated Cardiomyopathy Panel Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Dilated Cardiomyopathy Panel that also includes the following genes: SCN5A SGCD TAZ TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel United States.
Arrhythmogenic Right Ventricular Cardiomyopathy Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Arrhythmogenic Right Ventricular Cardiomyopathy that also includes the following genes: RYR2 TGFB3 TTN TMEM43 DSC2 DSG2 DSP JUP LMNA MYBPC3
More info about this panel United States.
Charcot-Marie-Tooth Syndrome Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Charcot-Marie-Tooth Syndrome that also includes the following genes: SPTLC1 YARS PRX BSCL2 GDAP1 KIF1B LITAF FIG4 MFN2 TRPV4
More info about this panel United States.
Comprehensive Neuromuscular Panel Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Comprehensive Neuromuscular Panel that also includes the following genes: RYR1 RYR2 BIN1 SCN4A SGCA SGCB SGCD SGCE SGCG TCAP
More info about this panel United States.
Congenital Muscular Dystrophy Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Congenital Muscular Dystrophy that also includes the following genes: RYR1 TCAP SELENON FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2 COL6A3
More info about this panel United States.
Limb-Girdle Muscular Dystrophy Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Limb-Girdle Muscular Dystrophy that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN VCP CAPN3 CAV3
More info about this panel United States.
Non-Compaction Arrhythmogenic Left Ventricular Cardiomyopathy Panel
United States.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University Non-Compaction Arrhythmogenic Left Ventricular Cardiomyopathy that also includes the following genes: TAZ TNNT2 TPM1 VCL ACTC1 LDB3 ACTN2 DTNA LMNA MYBPC3
More info about this panel United States.
Arrhymogenic Right Ventricular Cardiomyopathy Panel Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Arrhymogenic Right Ventricular Cardiomyopathy Panel that also includes the following genes: RYR2 TGFB3 TTN LDB3 DES TMEM43 DSC2 DSG2 DSP JUP
More info about this panel United States.
LMNA Sequencing Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center
This panel specifically test the LMNA gene.
More info about this panel United States.
Atrioventricular Block Panel Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Atrioventricular Block Panel that also includes the following genes: SCN1B SCN5A TRPM4 NKX2-5 DES EMD LMNA
More info about this panel United States.
Left Ventricular Noncompaction (13 genes) Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Left Ventricular Noncompaction (13 genes) that also includes the following genes: TAZ TNNT2 VCL ACTC1 LDB3 ACTN2 DES LMNA MYBPC3 MYH7
More info about this panel United States.
Dilated Cardiomyopathy Panel (30 genes) Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Dilated Cardiomyopathy Panel (30 genes) that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL
More info about this panel United States.
Comprehensive Cardiomyopathy Panel (37 genes) Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Comprehensive Cardiomyopathy Panel (37 genes) that also includes the following genes: SCN5A SCO2 SGCD SURF1 TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1
More info about this panel United States.
DCM and DMD related Cardiomyopathy Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center DCM and DMD related Cardiomyopathy that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL
More info about this panel United States.
Atrial Fibrillation Panel Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Atrial Fibrillation Panel that also includes the following genes: SCN1B SCN2B SCN5A SCN3B GJA5 ABCC9 KCNA5 KCND3 KCNE1 KCNE2
More info about this panel United States.
Partial Lipodystrophy Deletion/Duplication Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Partial Lipodystrophy Deletion/Duplication Panel that also includes the following genes: ZMPSTE24 CAV1 TBC1D4 CIDEC ADRA2A AKT2 LIPE LMNA LMNB2 PIK3R1
More info about this panel United States.
Comprehensive Lipodystrophy Deletion/Duplication Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Comprehensive Lipodystrophy Deletion/Duplication Panel that also includes the following genes: ZMPSTE24 CAV1 BSCL2 TBC1D4 CIDEC ADRA2A AGPAT2 FBN1 AKT2 KCNJ6
More info about this panel United States.
Comprehensive Lipodystrophy Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Comprehensive Lipodystrophy Panel that also includes the following genes: ZMPSTE24 CAV1 BSCL2 TBC1D4 CIDEC ADRA2A AGPAT2 FBN1 AKT2 KCNJ6
More info about this panel United States.
Partial Lipodystrophy Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Partial Lipodystrophy Panel that also includes the following genes: ZMPSTE24 CAV1 TBC1D4 CIDEC ADRA2A AKT2 LIPE LMNA LMNB2 PIK3R1
More info about this panel United States.
Abnormal/Ambiguous Genitalia Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Abnormal/Ambiguous Genitalia Sequencing Panel that also includes the following genes: ROR2 SALL1 BMP4 SEMA3A SOX9 SRD5A2 SRY STAR TBX15 CEP41
More info about this panel United States.
Premature Ovarian Failure Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Premature Ovarian Failure Sequencing Panel that also includes the following genes: BMP15 FOXL2 MCM8 PSMC3IP HFM1 NOBOX FIGLA FSHR LMNA NR5A1
More info about this panel United States.
LMNA deletion/duplication analysis Panel
United States.
By Genetic Services Laboratory University of Chicago
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA sequencing Panel
United States.
By Genetic Services Laboratory University of Chicago
This panel specifically test the LMNA gene.
More info about this panel United States.
Neuromuscular Disorders Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Neuromuscular Disorders Sequencing Panel that also includes the following genes: RYR1 BIN1 SCN4A SGCA SGCB SGCD SGCG SNAP25 STIM1 SYT2
More info about this panel United States.
Congenital Muscular Dystrophy Deletion/Duplication Analysis Panel
United States.
By Genetic Services Laboratory University of Chicago Congenital Muscular Dystrophy Deletion/Duplication Analysis that also includes the following genes: RYR1 RXYLT1 SELENON SYNE1 FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2
More info about this panel United States.
Congenital Muscular Dystrophy Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Congenital Muscular Dystrophy Sequencing Panel that also includes the following genes: RYR1 RXYLT1 SELENON SYNE1 FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2
More info about this panel United States.
Congenital Myopathy with Prominent Contractures Deletion/Duplication Analysis Panel
United States.
By Genetic Services Laboratory University of Chicago Congenital Myopathy with Prominent Contractures Deletion/Duplication Analysis that also includes the following genes: RYR1 SELENON SYNE2 SYNE1 COL6A1 COL6A2 COL6A3 TMEM43 KLHL40 EMD
More info about this panel United States.
Congenital Myopathy with Prominent Contractures Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Congenital Myopathy with Prominent Contractures Sequencing Panel that also includes the following genes: RYR1 SELENON SYNE2 SYNE1 COL6A1 COL6A2 COL6A3 TMEM43 KLHL40 EMD
More info about this panel United States.
Limb-Girdle Muscular Dystrophy Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Limb-Girdle Muscular Dystrophy Sequencing Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Limb-Girdle Muscular Dystrophy Deletion/Duplication Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Limb-Girdle Muscular Dystrophy Deletion/Duplication Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Premature Ovarian Failure Deletion/Duplication Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Premature Ovarian Failure Deletion/Duplication Panel that also includes the following genes: BMP15 FOXL2 MCM8 PSMC3IP HFM1 NOBOX FIGLA FSHR LMNA NR5A1
More info about this panel United States.
Congenital Myopathy with Fiber-Type Disproportion Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Congenital Myopathy with Fiber-Type Disproportion Sequencing Panel that also includes the following genes: RYR1 TPM2 TPM3 ACTA1 SELENON LMNA MYH7
More info about this panel United States.
Emery-Dreifuss Muscular Dystrophy Sequencing Panel Panel
United States.
By Genetic Services Laboratory University of Chicago Emery-Dreifuss Muscular Dystrophy Sequencing Panel that also includes the following genes: SYNE2 SYNE1 TMEM43 EMD FHL1 LMNA
More info about this panel United States.
Targeted CM panel Panel
Italy.
By Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Targeted CM panel that also includes the following genes: SCN5A TNNI3 TNNT2 TPM1 LDB3 TMEM43 NEXN DSC2 DSG2 DSP
More info about this panel Italy.
Cardiac Arrhythmia Gene Panel Panel
New Zealand.
By Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital Cardiac Arrhythmia Gene Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN5A TNNI3 TNNT2 TPM1 CACNA1C CACNB2 CASQ2
More info about this panel New Zealand.
Familial Partial Lipodystrophy Type 2 Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the LMNA gene.
More info about this panel Germany.
Mandibuloacral Dysplasia Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen Mandibuloacral Dysplasia that also includes the following genes: ZMPSTE24 LMNA
More info about this panel Germany.
LMNA-Related Dilated Cardiomyopathy Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the LMNA gene.
More info about this panel Germany.
Lethal Restrictive Dermopathy, LMNA-Related Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the LMNA gene.
More info about this panel Germany.
LMNA Panel
Germany.
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the LMNA gene.
More info about this panel Germany.
Charcot Marie Tooth Panel Panel
Argentina.
By Molecular Genetics Laboratory Centro de Investigaciones Endocrinologicas "Dr. Cesar Bergada" Charcot Marie Tooth Panel that also includes the following genes: SPTLC1 TTR PRX GDAP1 KIF1B LITAF FIG4 MFN2 TRPV4 FGD4
More info about this panel Argentina.
DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes) Panel
United States.
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes) that also includes the following genes: RYR2 SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TRDN
More info about this panel United States.
Pan Cardiomyopathy Panel (62 Genes) Panel
United States.
By Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine Pan Cardiomyopathy Panel (62 Genes) that also includes the following genes: RYR2 SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TRDN
More info about this panel United States.
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication Panel
United States.
By ARUP Laboratories, Molecular Genetics and Genomics Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SCO2 SGCA SGCB SGCD SGCG
More info about this panel United States.
LMNA-Related Disorders (LMNA) Sequencing Panel
United States.
By ARUP Laboratories, Molecular Genetics and Genomics
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA-Related Disorders (LMNA) Del/Dup Panel
United States.
By ARUP Laboratories, Molecular Genetics and Genomics
This panel specifically test the LMNA gene.
More info about this panel United States.
Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies, PMP22 Deletion/Duplication with Reflex to Sequencing Panel Panel
United States.
By ARUP Laboratories, Molecular Genetics and Genomics Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies, PMP22 Deletion/Duplication with Reflex to Sequencing Panel that also includes the following genes: SBF1 SCN9A SLC12A6 SOX10 ATL1 SPTLC1 SPTLC2 TFG YARS PRX
More info about this panel United States.
Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies Panel, Sequencing Panel
United States.
By ARUP Laboratories, Molecular Genetics and Genomics Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies Panel, Sequencing that also includes the following genes: SBF1 SCN9A SLC12A6 SOX10 ATL1 SPTLC1 SPTLC2 TFG YARS PRX
More info about this panel United States.
Comprehensive Cardiomyopathy Panel Panel
United States.
By GeneDx Comprehensive Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A SGCD BRAF SOS1 TAZ TCAP TMPO TNNC1 TNNI3
More info about this panel United States.
DCM/LVNC Sequencing Panel Panel
United States.
By GeneDx DCM/LVNC Sequencing Panel that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panel United States.
ARVCNext Panel
United States.
By Ambry Genetics ARVCNext that also includes the following genes: RYR2 TGFB3 TMEM43 DSC2 DSG2 DSP JUP LMNA PKP2
More info about this panel United States.
CardioNext with TTN Panel
United States.
By Ambry Genetics CardioNext with TTN that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SNTA1 TAZ TBX1 TBX20 TBX5
More info about this panel United States.
CMNext with TTN Panel
United States.
By Ambry Genetics CMNext with TTN that also includes the following genes: RYR2 SCN5A TAZ TBX20 TCAP TGFB3 TMPO TNNC1 TNNI3 TNNT2
More info about this panel United States.
CustomNext: Cardio Panel
United States.
By Ambry Genetics CustomNext: Cardio that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SKI SNTA1 TAZ TBX1 TBX20
More info about this panel United States.
DCMNext with TTN Panel
United States.
By Ambry Genetics DCMNext with TTN that also includes the following genes: SCN5A TAZ TBX20 TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel United States.
RhythmNext Panel
United States.
By Ambry Genetics RhythmNext that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TBX5 TGFB3 TRDN CACNA1C CACNA2D1
More info about this panel United States.
RhythmFirst reflex RhythmNext Panel
United States.
By Ambry Genetics RhythmFirst reflex RhythmNext that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TBX5 TGFB3 TRDN CACNA1C CACNA2D1
More info about this panel United States.
LVNCNext Panel
United States.
By Ambry Genetics LVNCNext that also includes the following genes: TAZ TNNT2 TPM1 ACTC1 LDB3 LMNA MYBPC3 MYH7
More info about this panel United States.
LMNA mutation analysis Panel
Netherlands.
By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam
This panel specifically test the LMNA gene.
More info about this panel Netherlands.
Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis Panel
Netherlands.
By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panel Netherlands.
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis Panel
Netherlands.
By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TNNT2 TRDN CACNA1C
More info about this panel Netherlands.
Detection of the c.892C>T mutation in exon 5 of the LMNA gene Panel
Cyprus.
By Neurogenetics Department Cyprus Institute of Neurology and Genetics
This panel specifically test the LMNA gene.
More info about this panel Cyprus.
LMNA. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the LMNA gene.
More info about this panel Spain.
LMNA. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the LMNA gene.
More info about this panel Spain.
LMNA. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the LMNA gene.
More info about this panel Spain.
LMNA, MYBPC3, MYH7, SCN5A, TNNI3, TNNT2. NextGeneDx.Complete sequencing by NGS Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica LMNA, MYBPC3, MYH7, SCN5A, TNNI3, TNNT2. NextGeneDx.Complete sequencing by NGS that also includes the following genes: SCN5A TNNI3 TNNT2 LMNA MYBPC3 MYH7
More info about this panel Spain.
LMNA. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the LMNA gene.
More info about this panel Spain.
ACTC1, DTNA, LDB3, LMNA, MYH7, TAZ, TNNT2. NextGeneDx.Complete sequencing by NGS Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica ACTC1, DTNA, LDB3, LMNA, MYH7, TAZ, TNNT2. NextGeneDx.Complete sequencing by NGS that also includes the following genes: TAZ TNNT2 ACTC1 LDB3 DTNA LMNA MYH7
More info about this panel Spain.
Lethal Restrictive Dermopathy, LMNA-Related Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Hutchinson-Gilford progeria (sequence analysis of LMNA gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Mandibuloacral Dysplasia Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Charcot-Marie-Tooth disease type 2B1 (CMT2B1, sequence analysis of LMNA gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Charcot-Marie-Tooth Neuropathy Type 2B1 Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Emery-Dreifuss muscular dystrophy (sequence analysis of LMNA gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Limb-girdle muscular dystrophy type 1B (LGMD1B, sequence analysis of LMNA gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Familial Partial Lipodystrophy Type 2 Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Familial dilated cardiomyopathy (sequence analysis of LMNA, exons 13, 16 and 23 of MYH7 gene and exons 9, 10, 13 and 15 of TNNT2 gene) Panel
Portugal.
By CGC Genetics Familial dilated cardiomyopathy (sequence analysis of LMNA, exons 13, 16 and 23 of MYH7 gene and exons 9, 10, 13 and 15 of TNNT2 gene) that also includes the following genes: TNNT2 LMNA MYH7
More info about this panel Portugal.
Left ventricular noncompaction (LVNC, NGS panel for 13 genes) Panel
Portugal.
By CGC Genetics Left ventricular noncompaction (LVNC, NGS panel for 13 genes) that also includes the following genes: SGCD TAZ TCAP TNNT2 TPM1 ACTC1 LDB3 CSRP3 DTNA LMNA
More info about this panel Portugal.
Dilated cardiomyopathy (CMD, NGS panel for 22 genes) Panel
Portugal.
By CGC Genetics Dilated cardiomyopathy (CMD, NGS panel for 22 genes) that also includes the following genes: SGCD TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL ACTC1 LDB3
More info about this panel Portugal.
Dilated cardiomyopathy (CMD, NGS panel for 10 genes) Panel
Portugal.
By CGC Genetics Dilated cardiomyopathy (CMD, NGS panel for 10 genes) that also includes the following genes: SGCD TCAP TNNT2 TPM1 ACTC1 CSRP3 LMNA MYBPC3 MYH7 PLN
More info about this panel Portugal.
Familial dilated cardiomyopathy (deletion/duplication analysis of LMNA gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
LMNA gene (deletion/duplication analysis) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Familial dilated cardiomyopathy (deletion/duplication analysis of LMNA gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Atypical hemolytic uremic syndrome (NGS panel for 14 genes) Panel
Portugal.
By CGC Genetics Atypical hemolytic uremic syndrome (NGS panel for 14 genes) that also includes the following genes: CFB THBD C3 ADAMTS13 CFHR4 CFHR3 MMACHC CFHR5 DGKE CFH
More info about this panel Portugal.
Hereditary peripheral neuropathies, including Charcot-Marie-Tooth disease (NGS panel for 74 genes) Panel
Portugal.
By CGC Genetics Hereditary peripheral neuropathies, including Charcot-Marie-Tooth disease (NGS panel for 74 genes) that also includes the following genes: SBF1 SCN11A SCN9A DST SLC12A6 SOX10 ATL1 SPTLC1 SPTLC2 TWNK
More info about this panel Portugal.
Limb-girdle muscular dystrophies (NGS panel for 26 genes) Panel
Portugal.
By CGC Genetics Limb-girdle muscular dystrophies (NGS panel for 26 genes) that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Portugal.
Sequence analysis of LMNA gene (lamin A/C) Panel
Portugal.
By CGC Genetics
This panel specifically test the LMNA gene.
More info about this panel Portugal.
Cardiomyopathy and changes in cardiac conduction (NGS panel for 59 genes) Panel
Portugal.
By CGC Genetics Cardiomyopathy and changes in cardiac conduction (NGS panel for 59 genes) that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SGCD SNTA1 TCAP TNNC1 TNNI3 TNNT2
More info about this panel Portugal.
Charcot-Marie-Tooth disease (NGS panel for 43 genes) Panel
Portugal.
By CGC Genetics Charcot-Marie-Tooth disease (NGS panel for 43 genes) that also includes the following genes: SBF1 YARS PRX GDAP1 TRIM2 KIF1B LITAF FIG4 MFN2 TRPV4
More info about this panel Portugal.
Cardiomyopathy (hypertrophic, dilated and arrhythmogenic right ventricular dysplasia, NGS panel for 36 genes) Panel
Portugal.
By CGC Genetics Cardiomyopathy (hypertrophic, dilated and arrhythmogenic right ventricular dysplasia, NGS panel for 36 genes) that also includes the following genes: RYR2 SGCD TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL MYOZ2
More info about this panel Portugal.
Congenital muscular dystrophies (NGS panel for 31 genes) Panel
Portugal.
By CGC Genetics Congenital muscular dystrophies (NGS panel for 31 genes) that also includes the following genes: TCAP TTN SELENON SYNE2 SYNE1 FKRP POMGNT1 CHKB POMT2 COL6A1
More info about this panel Portugal.
Lipodystrophies (NGS panel for 17 genes) Panel
Portugal.
By CGC Genetics Lipodystrophies (NGS panel for 17 genes) that also includes the following genes: ZMPSTE24 CAV1 BSCL2 TBC1D4 CIDEC AGPAT2 FBN1 AKT2 LIPE LMNA
More info about this panel Portugal.
Progeroid syndromes (NGS panel for 12 genes) Panel
Portugal.
By CGC Genetics Progeroid syndromes (NGS panel for 12 genes) that also includes the following genes: BLM WRN ZMPSTE24 CAV1 BANF1 SPRTN ERCC6 ERCC8 FBN1 KCNJ6
More info about this panel Portugal.
Lipodystrophies and progeroid syndromes (NGS panel for 25 genes) Panel
Portugal.
By CGC Genetics Lipodystrophies and progeroid syndromes (NGS panel for 25 genes) that also includes the following genes: BLM WRN ZMPSTE24 CAV1 BSCL2 BANF1 TBC1D4 CIDEC SPRTN AGPAT2
More info about this panel Portugal.
Progeroid syndromes (NGS panel for 12 genes) Panel
Portugal.
By CGC Genetics Progeroid syndromes (NGS panel for 12 genes) that also includes the following genes: BLM WRN ZMPSTE24 CAV1 BANF1 SPRTN ERCC6 ERCC8 FBN1 KCNJ6
More info about this panel Portugal.
Lipodystrophies (NGS panel for 17 genes) Panel
Portugal.
By CGC Genetics Lipodystrophies (NGS panel for 17 genes) that also includes the following genes: ZMPSTE24 CAV1 BSCL2 TBC1D4 CIDEC AGPAT2 FBN1 AKT2 LIPE LMNA
More info about this panel Portugal.
Lipodystrophies and progeroid syndromes (NGS panel for 25 genes) Panel
Portugal.
By CGC Genetics Lipodystrophies and progeroid syndromes (NGS panel for 25 genes) that also includes the following genes: BLM WRN ZMPSTE24 CAV1 BSCL2 BANF1 TBC1D4 CIDEC SPRTN AGPAT2
More info about this panel Portugal.
Mandibuloacral Dysplasia Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA-Related Emery-Dreifuss Muscular Dystrophy, Autosomal Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
Progeroid Laminopathies Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
Familial Partial Lipodystrophy Type 2 Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA-Related Dilated Cardiomyopathy Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
Atypical Werner Syndrome Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
Charcot-Marie-Tooth Neuropathy Type 2B1 Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA-Related Muscle Diseases Panel
United States.
By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA full gene sequencing Panel
United States.
By University of Iowa Diagnostic Laboratories University of Iowa Hospitals and Clinics
This panel specifically test the LMNA gene.
More info about this panel United States.
LMNA-related disorders (LMNA) sequencing Panel
United States.
By University of Iowa Diagnostic Laboratories University of Iowa Hospitals and Clinics
This panel specifically test the LMNA gene.
More info about this panel United States.
Lipodystrophy, familial partial, 2 Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
This panel specifically test the LMNA gene.
More info about this panel Germany.
Test for Familial Partial Lipodystrophy Type 2 Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
This panel specifically test the LMNA gene.
More info about this panel Germany.
Muscular dystrophy, congenital Panel
Germany.
By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
This panel specifically test the LMNA gene.
More info about this panel Germany.
Familial Partial Lipodystrophy Type 2 Panel
United Kingdom.
By Exeter Molecular Genetics Laboratory
This panel specifically test the LMNA gene.
More info about this panel United Kingdom.
LMNA-Related Emery-Dreifuss Muscular Dystrophy, Autosomal Panel
United Kingdom.
By Exeter Molecular Genetics Laboratory
This panel specifically test the LMNA gene.
More info about this panel United Kingdom.
Congenital Myopathy Sequencing Panel Panel
United States.
By PreventionGenetics PreventionGenetics Congenital Myopathy Sequencing Panel that also includes the following genes: RYR1 BIN1 TNNT1 TPM2 TPM3 TTN ACTA1 CCDC78 MICU1 SELENON
More info about this panel United States.
Limb-Girdle Muscular Dystrophy (LGMD) Sequencing Panel Panel
United States.
By PreventionGenetics PreventionGenetics Limb-Girdle Muscular Dystrophy (LGMD) Sequencing Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN VCP CAPN3 DNAJB6
More info about this panel United States.
Charcot Marie Tooth - Comprehensive Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Charcot Marie Tooth - Comprehensive Sequencing Panel with CNV Detection that also includes the following genes: SBF1 YARS PRX GDAP1 TRIM2 LITAF FIG4 MFN2 TRPV4 FGD4
More info about this panel United States.
Charcot Marie Tooth - Axonal Neuropathy Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Charcot Marie Tooth - Axonal Neuropathy Sequencing Panel with CNV Detection that also includes the following genes: SBF1 PRX GDAP1 TRIM2 FIG4 MFN2 TRPV4 FGD4 AARS GNB4
More info about this panel United States.
Left Ventricular Noncompaction (LVNC) Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Left Ventricular Noncompaction (LVNC) Sequencing Panel with CNV Detection that also includes the following genes: TAZ TNNT2 VCL ACTC1 LDB3 DTNA LMNA MYBPC3 MYH7
More info about this panel United States.
Congenital Muscular Dystrophy Sequencing Panel Panel
United States.
By PreventionGenetics PreventionGenetics Congenital Muscular Dystrophy Sequencing Panel that also includes the following genes: RXYLT1 B4GAT1 FKRP POMGNT1 CHKB POMT2 COL12A1 COL6A1 COL6A2 COL6A3
More info about this panel United States.
Hutchinson-Gilford Progeria Syndrome (HGPS) via the LMNA Gene Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the LMNA gene.
More info about this panel United States.
Comprehensive Cardiology Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Comprehensive Cardiology Sequencing Panel with CNV Detection that also includes the following genes: RYR1 RYR2 SCN1B SCN2B SCN4B SCN5A SCO2 SGCD SGCG BRAF
More info about this panel United States.
Sudden Cardiac Arrest Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Sudden Cardiac Arrest Sequencing Panel with CNV Detection that also includes the following genes: RYR2 SCN2B SCN4B SCN5A SNTA1 TGFBR2 TNNC1 TNNI3 TNNT2 TPM1
More info about this panel United States.
Dilated Cardiomyopathy Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Dilated Cardiomyopathy Sequencing Panel with CNV Detection that also includes the following genes: SCN5A SGCD TAZ TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel United States.
Pan Cardiomyopathy Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Pan Cardiomyopathy Sequencing Panel with CNV Detection that also includes the following genes: RYR2 SCN5A SCO2 SGCD SGCG BRAF SOS1 TAZ TCAP TGFB3
More info about this panel United States.
Laminopathies via the LMNA Gene Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the LMNA gene.
More info about this panel United States.
Comprehensive Neuropathy Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Comprehensive Neuropathy Sequencing Panel with CNV Detection that also includes the following genes: SBF1 SCN9A SLC12A6 ATL1 SPTLC1 SPTLC2 TFG TTR YARS PRX
More info about this panel United States.
Comprehensive Neuromuscular Sequencing Panel Panel
United States.
By PreventionGenetics PreventionGenetics Comprehensive Neuromuscular Sequencing Panel that also includes the following genes: RYR1 BIN1 SCN4A SGCA SGCB SGCD SGCG SNAP25 SQSTM1 STIM1
More info about this panel United States.
Female Infertility Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Female Infertility Sequencing Panel with CNV Detection that also includes the following genes: BMP15 SEMA3A SEMA3E FOXL2 SOX10 SOX2 SOX3 SOX9 SRA1 SRD5A2
More info about this panel United States.
Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection that also includes the following genes: ROR2 SALL1 BMP15 BMP4 SEMA3A SEMA3E BMP7 FOXL2 BRDT SOS1
More info about this panel United States.
Disorders of Sex Development (DSD) Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Disorders of Sex Development (DSD) Sequencing Panel with CNV Detection that also includes the following genes: ROR2 SALL1 BMP15 BMP4 SEMA3A BMP7 FOXL2 SOS1 SOX10 SOX2
More info about this panel United States.
Premature Ovarian Failure (POF) Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Premature Ovarian Failure (POF) Sequencing Panel with CNV Detection that also includes the following genes: BMP15 FOXL2 STAG3 MCM8 PSMC3IP HFM1 CLPP MCM9 NOBOX FIGLA
More info about this panel United States.
Ambiguous Genitalia Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Ambiguous Genitalia Sequencing Panel with CNV Detection that also includes the following genes: ROR2 SALL1 BMP4 SEMA3A SOS1 SOX10 SOX2 SOX3 SOX9 SRD5A2
More info about this panel United States.
Atrioventricular block Deletion/ Duplication panel Panel
United States.
By Connective Tissue Gene Tests Atrioventricular block Deletion/ Duplication panel that also includes the following genes: SCN1B SCN5A TRPM4 NKX2-5 DES EMD LMNA
More info about this panel United States.
Congenital contracture syndrome extended NGS panel Panel
United States.
By Connective Tissue Gene Tests Congenital contracture syndrome extended NGS panel that also includes the following genes: TNNI2 TNNT3 TPM2 VPS33B ZMPSTE24 ADGRG6 NEK9 LGI4 NALCN CHRNA1
More info about this panel United States.
Congenital contracture syndrome extended Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Congenital contracture syndrome extended Comprehensive panel that also includes the following genes: TNNI2 TNNT3 TPM2 VPS33B ZMPSTE24 ADGRG6 NEK9 LGI4 NALCN CHRNA1
More info about this panel United States.
Congenital contracture syndrome extended Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Congenital contracture syndrome extended Deletion / Duplication panel that also includes the following genes: TNNI2 TNNT3 TPM2 VPS33B ZMPSTE24 ADGRG6 NEK9 LGI4 NALCN CHRNA1
More info about this panel United States.
Charcot-Marie-Tooth disease Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Charcot-Marie-Tooth disease Deletion / Duplication panel that also includes the following genes: SBF1 TFG YARS PRX BSCL2 GDAP1 TRIM2 KIF1B LITAF FIG4
More info about this panel United States.
Charcot-Marie-Tooth disease NGS panel Panel
United States.
By Connective Tissue Gene Tests Charcot-Marie-Tooth disease NGS panel that also includes the following genes: SBF1 TFG YARS PRX BSCL2 GDAP1 TRIM2 KIF1B LITAF FIG4
More info about this panel United States.
Charcot-Marie-Tooth disease Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Charcot-Marie-Tooth disease Comprehensive panel that also includes the following genes: SBF1 TFG YARS PRX BSCL2 GDAP1 TRIM2 KIF1B LITAF FIG4
More info about this panel United States.
Lethal congenital contracture syndrome and related disorders Comprehensive Panel Panel
United States.
By Connective Tissue Gene Tests Lethal congenital contracture syndrome and related disorders Comprehensive Panel that also includes the following genes: VPS33B ZMPSTE24 ADGRG6 NEK9 LGI4 CHRNA1 CHRND CHRNG VIPAS39 ADCY6
More info about this panel United States.
Lethal congenital contracture syndrome and related disorders NGS Panel Panel
United States.
By Connective Tissue Gene Tests Lethal congenital contracture syndrome and related disorders NGS Panel that also includes the following genes: VPS33B ZMPSTE24 ADGRG6 NEK9 LGI4 CHRNA1 CHRND CHRNG VIPAS39 ADCY6
More info about this panel United States.
Limb girdle muscular dystrophy Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Limb girdle muscular dystrophy Comprehensive panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Limb girdle muscular dystrophy Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Limb girdle muscular dystrophy Deletion / Duplication panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Limb girdle muscular dystrophy NGS panel Panel
United States.
By Connective Tissue Gene Tests Limb girdle muscular dystrophy NGS panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Lethal congenital contracture syndrome and related disorders Deletion / Duplication Panel Panel
United States.
By Connective Tissue Gene Tests Lethal congenital contracture syndrome and related disorders Deletion / Duplication Panel that also includes the following genes: VPS33B ZMPSTE24 ADGRG6 NEK9 LGI4 CHRNA1 CHRND CHRNG VIPAS39 ADCY6
More info about this panel United States.
Restrictive dermopathy, lethal NGS panel Panel
United States.
By Connective Tissue Gene Tests Restrictive dermopathy, lethal NGS panel that also includes the following genes: ZMPSTE24 LMNA
More info about this panel United States.
Restrictive dermopathy, lethal Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Restrictive dermopathy, lethal Comprehensive panel that also includes the following genes: ZMPSTE24 LMNA
More info about this panel United States.
Progeroid syndromes and related disorders NGS panel Panel
United States.
By Connective Tissue Gene Tests Progeroid syndromes and related disorders NGS panel that also includes the following genes: WRN ZMPSTE24 BSCL2 BANF1 B3GALT6 SLC25A24 AGPAT2 ERCC2 ERCC3 ERCC4
More info about this panel United States.
Progeroid syndromes and related disorders Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Progeroid syndromes and related disorders Comprehensive panel that also includes the following genes: WRN ZMPSTE24 BSCL2 BANF1 B3GALT6 SLC25A24 AGPAT2 ERCC2 ERCC3 ERCC4
More info about this panel United States.
Progeroid syndromes and related disorders Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Progeroid syndromes and related disorders Deletion / Duplication panel that also includes the following genes: WRN ZMPSTE24 BSCL2 BANF1 B3GALT6 SLC25A24 AGPAT2 ERCC2 ERCC3 ERCC4
More info about this panel United States.
Restrictive dermopathy, lethal Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Restrictive dermopathy, lethal Deletion / Duplication panel that also includes the following genes: ZMPSTE24 LMNA
More info about this panel United States.
Lipodystrophy Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen Lipodystrophy that also includes the following genes: LMNA PPARG
More info about this panel Germany.
LMNA-related Muscular dystrophy Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen
This panel specifically test the LMNA gene.
More info about this panel Germany.
Lipodystrophy - panel diagnostics Panel
Germany.
By Institute of Human Genetics Uniklinik RWTH Aachen Lipodystrophy - panel diagnostics that also includes the following genes: CIDEC AKT2 LMNA PLIN1 PPARG
More info about this panel Germany.
Histological Myofibrillar Myopathy Panel
Germany.
By MGZ Medical Genetics Center Histological Myofibrillar Myopathy that also includes the following genes: MYOT TTN VCP LDB3 GNE CRYAB DES FHL1 FLNC LMNA
More info about this panel Germany.
Neuropathy Panel
Germany.
By MGZ Medical Genetics Center Neuropathy that also includes the following genes: SACS SCN10A SCN11A SCN9A SH3BP4 SLC12A6 SOD1 SPG11 ATL1 SPAST
More info about this panel Germany.
Muscular Dystrophy: Limb Girdle - autosomal dominant Panel
Germany.
By MGZ Medical Genetics Center Muscular Dystrophy: Limb Girdle - autosomal dominant that also includes the following genes: MYOT DNAJB6 CAV3 DES LMNA
More info about this panel Germany.
Muscular Dystrophy: Emery-Dreifuss Panel
Germany.
By MGZ Medical Genetics Center Muscular Dystrophy: Emery-Dreifuss that also includes the following genes: SYNE2 SYNE1 TMEM43 EMD FHL1 LMNA
More info about this panel Germany.
Newborn: Cardiomyopathy as presenting sign Panel
Germany.
By MGZ Medical Genetics Center Newborn: Cardiomyopathy as presenting sign that also includes the following genes: SCO2 SDHA SLC22A5 SLC25A3 TAZ TTN LPIN1 GFM1 SLC25A20 MTO1
More info about this panel Germany.
Myopathy – Rigid Spine Panel
Germany.
By MGZ Medical Genetics Center Myopathy – Rigid Spine that also includes the following genes: RYR1 SELENON COL6A1 COL6A2 COL6A3 EMD FHL1 GAA LAMA2 LMNA
More info about this panel Germany.
Charcot-Marie-Tooth Neuropathy Type 2B1 Panel
Germany.
By MGZ Medical Genetics Center
This panel specifically test the LMNA gene.
More info about this panel Germany.
Progeroid Laminopathies Panel
Germany.
By MGZ Medical Genetics Center
This panel specifically test the LMNA gene.
More info about this panel Germany.
Congenital muscular dystrophy, LMNA-related Panel
Germany.
By MGZ Medical Genetics Center
This panel specifically test the LMNA gene.
More info about this panel Germany.
Limb-girdle muscular dystrophy, type 1B Panel
Germany.
By MGZ Medical Genetics Center
This panel specifically test the LMNA gene.
More info about this panel Germany.
Heart Diseases - panels Panel
Germany.
By MGZ Medical Genetics Center Heart Diseases - panels that also includes the following genes: RIT1 RRAS RYR2 SCN4B SCN5A SCO2 SDHA BMPR2 SGCA SGCB
More info about this panel Germany.
Emery-Dreifuss Muscular Dystrophy Panel
Germany.
By MGZ Medical Genetics Center Emery-Dreifuss Muscular Dystrophy that also includes the following genes: SYNE2 SYNE1 TMEM43 EMD FHL1 LMNA
More info about this panel Germany.
Newborn: “Floppy Infant “ Panel
Germany.
By MGZ Medical Genetics Center Newborn: “Floppy Infant “ that also includes the following genes: RYR1 BIN1 SCN4A TCAP TNNT1 TPM2 TPM3 TTN UBA1 ACTA1
More info about this panel Germany.
Muscle Disease with Contractures and/or Rigid Spine Panel
Germany.
By MGZ Medical Genetics Center Muscle Disease with Contractures and/or Rigid Spine that also includes the following genes: RYR1 TNNT1 TPM2 TPM3 ACTA1 CAPN3 SELENON SYNE2 SYNE1 CFL2
More info about this panel Germany.
Spinal Muscular Atrophy, Proximal Motor Neuropathy Panel
Germany.
By MGZ Medical Genetics Center Spinal Muscular Atrophy, Proximal Motor Neuropathy that also includes the following genes: TFG VAPB SLC52A3 MFN2 CLP1 BICD2 TRPV4 LAS1L DYNC1H1 SLC52A2
More info about this panel Germany.
Muscle Weakness (Myopathy, Muscular Dystrophy) Panel
Germany.
By MGZ Medical Genetics Center Muscle Weakness (Myopathy, Muscular Dystrophy) that also includes the following genes: RYR1 BIN1 SCN4A SCO2 SDHA SGCA SGCB SGCD SGCG SLC22A5
More info about this panel Germany.
Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR) Panel
Germany.
By MGZ Medical Genetics Center Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR) that also includes the following genes: RYR1 SCN4A SGCA SGCB SGCD SGCG SLC22A5 STIM1 TCAP TIA1
More info about this panel Germany.
Dilated Cardiomyopathy Sequential Panel Panel
United States.
By FirmaLab Dilated Cardiomyopathy Sequential Panel that also includes the following genes: SCN5A TNNT2 TTN ACTC1 LMNA MYH7
More info about this panel United States.
Charcot Marie Tooth Type 2 Panel Panel
United States.
By FirmaLab Charcot Marie Tooth Type 2 Panel that also includes the following genes: YARS GDAP1 KIF1B MFN2 TRPV4 AARS MED25 DNM2 HSPB8 GARS
More info about this panel United States.
hypertrophic/dilated cardiomyopathy Panel
Germany.
By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München hypertrophic/dilated cardiomyopathy that also includes the following genes: TNNI3 TNNT2 LMNA MYBPC3 MYH7
More info about this panel Germany.
Limb Girdle Muscular Dystrophy Panel
India.
By GeneTech ATS GeneTech Private Limited
This panel specifically test the LMNA gene.
More info about this panel India.
Cardiac conduction abnormalities panel Panel
Netherlands.
By Genome Diagnostics Laboratory University Medical Center Utrecht Cardiac conduction abnormalities panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TGFB3 CACNA1A CACNA2D1 CACNB2 CASQ2
More info about this panel Netherlands.
Cardiomyopathy panel Panel
Netherlands.
By Genome Diagnostics Laboratory University Medical Center Utrecht Cardiomyopathy panel that also includes the following genes: RYR2 SCN5A SGCD TAZ TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1
More info about this panel Netherlands.
Emery-Dreifuss muscular dystrophy type 2 Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the LMNA gene.
More info about this panel Germany.
Cardiomyopathy, dilated type 1A Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the LMNA gene.
More info about this panel Germany.
Limb-girdle muscular dystrophy panel Panel
Germany.
By Centogene AG - the Rare Disease Company Limb-girdle muscular dystrophy panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Germany.
AllNeuro panel Panel
Germany.
By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1
More info about this panel Germany.
CHARCOT-MARIE-TOOTH DISEASE NEURONAL TYPE 2B1 Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the LMNA gene.
More info about this panel Germany.
Limb-girdle muscular dystrophy, autosomal dominant type 1B Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the LMNA gene.
More info about this panel Germany.
Muscular Dystrophies Panel Panel
Germany.
By CeGaT GmbH Muscular Dystrophies Panel that also includes the following genes: TCAP TTN SELENON SYNE2 SYNE1 FKRP POMGNT1 CHKB POMT2 COL6A1
More info about this panel Germany.
Limb-Girdle Muscular Dystrophies Panel Panel
Germany.
By CeGaT GmbH Limb-Girdle Muscular Dystrophies Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Germany.
Left Ventricular Noncompaction Cardiomyopathy (LVNC) Panel Panel
Germany.
By CeGaT GmbH Left Ventricular Noncompaction Cardiomyopathy (LVNC) Panel that also includes the following genes: TAZ TNNT2 TPM1 PRDM16 ACTC1 LDB3 MIB1 DTNA LMNA MYBPC3
More info about this panel Germany.
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Panel Panel
Germany.
By CeGaT GmbH Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Panel that also includes the following genes: RYR2 TGFB3 TTN CTNNA3 DES TMEM43 DSC2 DSG2 DSP JUP
More info about this panel Germany.
Charcot-Marie-Tooth and Sensory Neuropathies Panel Panel
Germany.
By CeGaT GmbH Charcot-Marie-Tooth and Sensory Neuropathies Panel that also includes the following genes: SBF1 SCN10A SCN11A SCN9A DST SLC12A6 SOX10 ATL1 SPTLC1 SPTLC2
More info about this panel Germany.
Progeria syndromes Panel Panel
Germany.
By CeGaT GmbH Progeria syndromes Panel that also includes the following genes: BLM WRN ZMPSTE24 BANF1 GTF2H5 ERCC2 ERCC3 ERCC4 ERCC5 ERCC6
More info about this panel Germany.
LMNA - Gene sequencing Panel
Netherlands.
By Clinical Genetics Academic Medical Center
This panel specifically test the LMNA gene.
More info about this panel Netherlands.
Limb-Girdle Muscular Dystrophy type 1 Panel
Poland.
By Laboratory of Human Genetics GENOMED Health Care Center Limb-Girdle Muscular Dystrophy type 1 that also includes the following genes: MYOT DNAJB6 CAV3 TNPO3 DES HNRNPDL LMNA
More info about this panel Poland.
LMNA Panel
Spain.
By Innovagenomics Innovagenomics S.L
This panel specifically test the LMNA gene.
More info about this panel Spain.
Hypertrophic cardiomyopathy, LMNA Panel
Israel.
By GGA - Galil Genetic Analysis
This panel specifically test the LMNA gene.
More info about this panel Israel.
Mandibuloacral Dysplasia Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
LMNA-Related Dilated Cardiomyopathy Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
LMNA-Related Emery-Dreifuss Muscular Dystrophy, Autosomal Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
Familial Partial Lipodystrophy Type 2 Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
LMNA-Related Muscle Diseases Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
Charcot-Marie-Tooth Neuropathy Type 2B1 (LMNA) Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
LAMIN A/C Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
Limb girdle muscular dystrophy 1B Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner
This panel specifically test the LMNA gene.
More info about this panel Germany.
Limb girdle muscular dystrophy-Panel Panel
Germany.
By MVZ Dortmund Dr. Eberhard & Partner Limb girdle muscular dystrophy-Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT CAPN3 DNAJB6 CAV3 TRIM32
More info about this panel Germany.
Charcot-Marie-Tooth Disease Panel
Estonia.
By Asper Biogene Asper Biogene LLC Charcot-Marie-Tooth Disease that also includes the following genes: SBF1 SCN9A SPTLC1 SPTLC2 SURF1 TFG VCP YARS PRX SLC5A7
More info about this panel Estonia.
Arrhythmia Panel
Estonia.
By Asper Biogene Asper Biogene LLC Arrhythmia that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SNTA1 TGFB3 CACNA1C CACNB2 CASQ2
More info about this panel Estonia.
Arrhythmogenic Right Ventricular Dysplasia/ Cardiomyopathy Panel
Estonia.
By Asper Biogene Asper Biogene LLC Arrhythmogenic Right Ventricular Dysplasia/ Cardiomyopathy that also includes the following genes: RYR2 TGFB3 TTN LDB3 CTNNA3 DES TMEM43 DSC2 DSG2 DSP
More info about this panel Estonia.
Dilated Cardiomyopathy Panel
Estonia.
By Asper Biogene Asper Biogene LLC Dilated Cardiomyopathy that also includes the following genes: SCN5A SGCD TAZ TBX20 TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1
More info about this panel Estonia.
Limb-Girdle Muscular Dystrophy Panel
Estonia.
By Asper Biogene Asper Biogene LLC Limb-Girdle Muscular Dystrophy that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Estonia.
LMNA gene sequencing Panel
Spain.
By Health in Code
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated cardiomyopathy with conduction disorders Stage 1 Panel
Spain.
By Health in Code
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated cardiomyopathy with frequent ventricular arrhythmias Stage 1 Panel
Spain.
By Health in Code
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated cardiomyopathy associated with hypertrabeculation Stage 2 Panel
Spain.
By Health in Code
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated cardiomyopathy associated with skeletal myopathy and/or elevated CPK level Stage 1 Panel
Spain.
By Health in Code
This panel specifically test the LMNA gene.
More info about this panel Spain.
Left ventricular non-compaction adult Stage 2 Panel
Spain.
By Health in Code Left ventricular non-compaction adult Stage 2 that also includes the following genes: LDB3 LMNA
More info about this panel Spain.
Standard dilated cardiomyopathy Stage 1 Panel
Spain.
By Health in Code
This panel specifically test the LMNA gene.
More info about this panel Spain.
Left Ventricular Non-Compactation Panel Panel
Spain.
By Health in Code Left Ventricular Non-Compactation Panel that also includes the following genes: RYR2 TAZ TNNC1 TNNI3 TNNT2 TPM1 TTN PRDM16 ACTC1 CASQ2
More info about this panel Spain.
Auricular Fibrillation Panel Panel
Spain.
By Health in Code Auricular Fibrillation Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A TBX5 TNNI3 TNNT2 TPM1
More info about this panel Spain.
Restrictive Cardiomyopathy Panel Panel
Spain.
By Health in Code Restrictive Cardiomyopathy Panel that also includes the following genes: TNNC1 TNNI3 TNNT2 TPM1 TTN TTR ACTC1 ACTN2 MYPN DES
More info about this panel Spain.
Inherited Cardiovascular Diseases and Sudden Death Panel Panel
Spain.
By Health in Code Inherited Cardiovascular Diseases and Sudden Death Panel that also includes the following genes: MRPL3 RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A BMPR1B BMPR2 SGCA
More info about this panel Spain.
Dilated Cardiomyopathy Panel Panel
Spain.
By Health in Code Dilated Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A SGCA SGCB SGCD SLC22A5 BRAF TAZ TBX20 TCAP
More info about this panel Spain.
Skeletal Myopathy Panel Panel
Spain.
By Health in Code Skeletal Myopathy Panel that also includes the following genes: SGCA SGCB SGCD SLC22A5 SLC25A4 SURF1 TAZ TCAP TNNI3 MYOT
More info about this panel Spain.
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease Panel
Spain.
By Health in Code Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease that also includes the following genes: MRPL3 RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SLC22A5 BRAF SLC25A4
More info about this panel Spain.
Cardiac Conduction Disease Panel Panel
Spain.
By Health in Code Cardiac Conduction Disease Panel that also includes the following genes: SCN10A SCN1B SCN4B SCN5A TBX5 TTR CACNA1D ACTC1 LDB3 HCN4
More info about this panel Spain.
Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease Panel
Spain.
By Health in Code Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TNNC1 TNNI3 TNNT2
More info about this panel Spain.
Cardiomyopathies Panel Panel
Spain.
By Health in Code Cardiomyopathies Panel that also includes the following genes: MRPL3 RYR2 SCN5A SGCA SGCB SGCD SLC22A5 BRAF SLC25A4 SOS1
More info about this panel Spain.
Arrythmogenic Cardiomyopathy Panel Panel
Spain.
By Health in Code Arrythmogenic Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A TGFB3 TTN CASQ2 LDB3 CTNNA3 DES TMEM43 DSC2
More info about this panel Spain.
Hypertrophic Cardiomyopathy Extended Panel Panel
Spain.
By Health in Code Hypertrophic Cardiomyopathy Extended Panel that also includes the following genes: MRPL3 RYR2 SLC22A5 BRAF SLC25A4 SOS1 SURF1 TAZ TCAP KLF10
More info about this panel Spain.
Arrhythmogenic cardiomyopathy Panel
Spain.
By Health in Code Arrhythmogenic cardiomyopathy that also includes the following genes: RYR2 SCN5A TGFB3 TTN CASQ2 LDB3 PERP PPP1R13L CTNNA3 CTNNB1
More info about this panel Spain.
Mixed hyperlipidemias Panel
Spain.
By Health in Code Mixed hyperlipidemias that also includes the following genes: ZMPSTE24 CAV1 BSCL2 INSIG2 CIDEC AGPAT2 AKT2 INSR LEP LMNA
More info about this panel Spain.
Ventricular arrhythmia and sudden death without structural heart disease Panel
Spain.
By Health in Code Ventricular arrhythmia and sudden death without structural heart disease that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TBX5 TNNC1 TNNI3
More info about this panel Spain.
Cardiovascular Diseases_General Panel Panel
Spain.
By Health in Code Cardiovascular Diseases_General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR1 RYR2 SAR1B BLK SCN10A SCN1B SCN2B
More info about this panel Spain.
Non-compaction cardiomyopathy Panel
Spain.
By Health in Code Non-compaction cardiomyopathy that also includes the following genes: RYR2 TAZ TNNC1 TNNI3 TNNT2 TPM1 TTN PRDM16 ACTC1 CASQ2
More info about this panel Spain.
Skeletal myopathy Panel Panel
Spain.
By Health in Code Skeletal myopathy Panel that also includes the following genes: SCO2 SDHA SGCA SGCB SGCD SLC22A5 SLC25A3 SLC25A4 SURF1 TAZ
More info about this panel Spain.
Dyslipidemias / Early atherosclerosis Panel
Spain.
By Health in Code Dyslipidemias / Early atherosclerosis that also includes the following genes: RYR1 SAR1B BLK SLCO1B1 SLC22A8 SLC2A2 HNF1A HNF1B KLF11 WFS1
More info about this panel Spain.
Cardiac conduction disease Panel Panel
Spain.
By Health in Code Cardiac conduction disease Panel that also includes the following genes: SCN10A SCN1B SCN4B SCN5A TBX5 TTR CACNA1D ACTC1 IRX3 KCNK17
More info about this panel Spain.
Atrial fibrillation Panel Panel
Spain.
By Health in Code Atrial fibrillation Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A TBX5 TNNI3 TNNT2 TPM1
More info about this panel Spain.
Dilated Cardiomyopathy Panel Panel
Spain.
By Health in Code Dilated Cardiomyopathy Panel that also includes the following genes: TAZ TNNC1 TNNI3 TNNT2 TPM1 TTN ACTA1 ACTC1 CAV3 ANKRD1
More info about this panel Spain.
Arrhythmia General Panel Panel
Spain.
By Health in Code Arrhythmia General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SCO2
More info about this panel Spain.
Hypertrophic cardiomyopathy extended panel Panel
Spain.
By Health in Code Hypertrophic cardiomyopathy extended panel that also includes the following genes: MRPL3 RYR2 SCO2 SLC22A5 BRAF SLC25A3 SLC25A4 SOS1 SURF1 TAZ
More info about this panel Spain.
Resctrictive cardiomyopathy Panel
Spain.
By Health in Code Resctrictive cardiomyopathy that also includes the following genes: TNNC1 TNNI3 TNNT2 TPM1 TTN TTR ACTC1 ACTN2 MYPN DES
More info about this panel Spain.
Cardiomyopathies General Panel Panel
Spain.
By Health in Code Cardiomyopathies General Panel that also includes the following genes: RIT1 MRPL3 RRAS RYR2 SCN5A SCO2 SDHA SGCA SGCB SGCD
More info about this panel Spain.
LMNA-Related Dilated Cardiomyopathy Panel
Netherlands.
By Clinical Genomics Maastricht University Medical Centre
This panel specifically test the LMNA gene.
More info about this panel Netherlands.
Lethal Restrictive Dermopathy, LMNA-Related Panel
Netherlands.
By Clinical Genomics Maastricht University Medical Centre
This panel specifically test the LMNA gene.
More info about this panel Netherlands.
LMNA-Related Muscle Diseases Panel
Netherlands.
By Clinical Genomics Maastricht University Medical Centre
This panel specifically test the LMNA gene.
More info about this panel Netherlands.
aHUS/DDD Genetic Evaluation Panel
United States.
By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti aHUS/DDD Genetic Evaluation that also includes the following genes: CFB THBD C3 C4BPA C4BPB ADAMTS13 CFHR4 CFHR3 CFHR5 DGKE
More info about this panel United States.
aCGH Deletion/Duplication Analysis Panel
United States.
By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti aCGH Deletion/Duplication Analysis that also includes the following genes: CFB RUNX1 STXBP2 TBXA2R THBD VWF WAS C3 C4BPA C4BPB
More info about this panel United States.
Cardiomyopathy, dilated, 1A Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Cardiomyopathy, dilated, 1A Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Charcot-Marie-Tooth 2B1 Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Hutchinson-Gilford progeria syndrome Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Lipodystrophy, familial partial, 2 Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Muscular dystrophy, congenital Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Muscular dystrophy, limb-girdle 1B Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Restrictive dermopathy, lethal Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
Emery-Dreifuss muscular dystrophy Panel
Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the LMNA gene.
More info about this panel Austria.
LMNA Gene Sequencing Panel
Colombia.
By GENETIX Centro de Investigación en Genética Humana y Reproductiva
This panel specifically test the LMNA gene.
More info about this panel Colombia.
LMNA Panel
Austria.
By Division Human Genetics Medical University Innsbruck
This panel specifically test the LMNA gene.
More info about this panel Austria.
Cardiomyopathy, dilated, 1A Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Charcot-Marie-Tooth 2B1 Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Emery-Dreifuss muscular dystrophy Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Hutchinson-Gilford progeria syndrome Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Lipodystrophy, familial partial, 2 Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Muscular dystrophy, congenital Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Muscular dystrophy, limb-girdle 1B Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Restrictive dermopathy, lethal Panel
Slovakia.
By MedGene
This panel specifically test the LMNA gene.
More info about this panel Slovakia.
Invitae Arrhythmia Comprehensive Panel Panel
United States.
By Invitae Invitae Arrhythmia Comprehensive Panel that also includes the following genes: RYR2 SCN5A TNNI3 TNNT2 TRDN TTN CACNA1C CACNB2 CALM1 CALM2
More info about this panel United States.
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel Panel
United States.
By Invitae Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel that also includes the following genes: RYR2 SCN5A SGCD SLC22A5 TAZ TCAP TGFB3 TNNC1 TNNI3 TNNT2
More info about this panel United States.
Invitae Arrhythmogenic Cardiomyopathy Panel Panel
United States.
By Invitae Invitae Arrhythmogenic Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A TNNI3 TNNT2 TTN ACTN2 RBM20 DES TMEM43 DSC2
More info about this panel United States.
Invitae Cardiomyopathy Comprehensive Panel Panel
United States.
By Invitae Invitae Cardiomyopathy Comprehensive Panel that also includes the following genes: RYR2 SCN5A SGCD SLC22A5 TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1
More info about this panel United States.
Invitae Dilated Cardiomyopathy Panel Panel
United States.
By Invitae Invitae Dilated Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A SGCD SLC22A5 TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1
More info about this panel United States.
Invitae Left Ventricular Noncompaction Panel Panel
United States.
By Invitae Invitae Left Ventricular Noncompaction Panel that also includes the following genes: RYR2 SCN5A TAZ TNNI3 TNNT2 TPM1 VCL ACTC1 HCN4 DSP
More info about this panel United States.
Invitae Comprehensive Neuromuscular Disorders Panel Panel
United States.
By Invitae Invitae Comprehensive Neuromuscular Disorders Panel that also includes the following genes: RYR1 BIN1 SCN4A SGCA SGCB SGCD SGCG SMN1 SMN2 SQSTM1
More info about this panel United States.
Invitae Comprehensive Neuropathies Panel Panel
United States.
By Invitae Invitae Comprehensive Neuropathies Panel that also includes the following genes: SCN11A SCN9A DST SPG11 ATL1 SPTLC1 SPTLC2 TFG TTR UBA1
More info about this panel United States.
Invitae Comprehensive Muscular Dystrophy Panel Panel
United States.
By Invitae Invitae Comprehensive Muscular Dystrophy Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN RXYLT1 CAPN3 DNAJB6
More info about this panel United States.
Invitae Congenital Muscular Dystrophy Panel Panel
United States.
By Invitae Invitae Congenital Muscular Dystrophy Panel that also includes the following genes: TCAP RXYLT1 B4GAT1 FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2 COL6A3
More info about this panel United States.
Invitae Emery-Dreifuss Muscular Dystrophy Panel Panel
United States.
By Invitae Invitae Emery-Dreifuss Muscular Dystrophy Panel that also includes the following genes: EMD FHL1 LMNA
More info about this panel United States.
Invitae Cardiomyopathy and Skeletal Muscle Disease Panel Panel
United States.
By Invitae Invitae Cardiomyopathy and Skeletal Muscle Disease Panel that also includes the following genes: RYR1 RYR2 BIN1 SCN5A SGCA SGCB SGCD SGCG SLC22A5 SQSTM1
More info about this panel United States.
Invitae Comprehensive Myopathy Panel Panel
United States.
By Invitae Invitae Comprehensive Myopathy Panel that also includes the following genes: RYR1 BIN1 SCN4A SQSTM1 STIM1 TIA1 TNNT1 TPM2 TPM3 MYOT
More info about this panel United States.
Invitae Limb-Girdle Muscular Dystrophy Panel Panel
United States.
By Invitae Invitae Limb-Girdle Muscular Dystrophy Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Invitae Congenital Fiber-Type Disproportion Panel Panel
United States.
By Invitae Invitae Congenital Fiber-Type Disproportion Panel that also includes the following genes: RYR1 TPM2 TPM3 ACTA1 SELENON LMNA MYH7
More info about this panel United States.
Invitae Charcot-Marie-Tooth Disease Comprehensive Panel Panel
United States.
By Invitae Invitae Charcot-Marie-Tooth Disease Comprehensive Panel that also includes the following genes: SPG11 TFG YARS PRX BSCL2 GDAP1 TRIM2 LITAF FIG4 MFN2
More info about this panel United States.
Invitae Charcot-Marie-Tooth Disease Autosomal Recessive Panel Panel
United States.
By Invitae Invitae Charcot-Marie-Tooth Disease Autosomal Recessive Panel that also includes the following genes: SPG11 PRX GDAP1 TRIM2 FIG4 MFN2 FGD4 SBF2 LRSAM1 MED25
More info about this panel United States.
Invitae Charcot-Marie-Tooth Disease Autosomal Dominant Panel Panel
United States.
By Invitae Invitae Charcot-Marie-Tooth Disease Autosomal Dominant Panel that also includes the following genes: TFG YARS BSCL2 GDAP1 LITAF MFN2 TRPV4 AARS GNB4 MORC2
More info about this panel United States.
Charcot Marie-Tooth disease: LMNA gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated cardiomyopathy: LMNA gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the LMNA gene.
More info about this panel Spain.
Emery-Dreifuss muscular dystrophy type 3, autosomal recessive: LMNA gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the LMNA gene.
More info about this panel Spain.
Emery-Dreyfuss muscular dystrophy type 2, autosomal dominant: LMNA gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the LMNA gene.
More info about this panel Spain.
Limb-girdle muscular dystrophy type 1B (LGMD 1B): LMNA gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the LMNA gene.
More info about this panel Spain.
Lipodystrophy, Familial partial, Dunnigan type: LMNA gene sequence analysis Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the LMNA gene.
More info about this panel Spain.
CARDIOMYOPATHY, DILATED (DCM Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases CARDIOMYOPATHY, DILATED (DCM that also includes the following genes: SCN5A SGCD TAZ TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel Spain.
CHARCOT- MARIE TOOTH Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases CHARCOT- MARIE TOOTH that also includes the following genes: YARS PRX BSCL2 GDAP1 KIF1B LITAF FIG4 MFN2 TRPV4 FGD4
More info about this panel Spain.
LIMB-GIRDLE MUSCULAR DYSTROPHY Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases LIMB-GIRDLE MUSCULAR DYSTROPHY that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Spain.
LYMPHEDEMA Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases LYMPHEDEMA that also includes the following genes: SOX18 ZMPSTE24 GJC2 CCBE1 FLT4 FOXC2 GATA2 KIF11 LMNA
More info about this panel Spain.
LIMB-GIRDLE MUSCULAR DYSTROPHY, A.D. Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases LIMB-GIRDLE MUSCULAR DYSTROPHY, A.D. that also includes the following genes: MYOT DNAJB6 CAV3 DES LMNA
More info about this panel Spain.
Left ventricular noncompaction Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Left ventricular noncompaction that also includes the following genes: TAZ TNNT2 TPM1 ACTC1 LDB3 DTNA LMNA MYBPC3 MYH7
More info about this panel Spain.
Lipodystrophy, familial partial Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Lipodystrophy, familial partial that also includes the following genes: CIDEC LIPE LMNA PLIN1 PPARG
More info about this panel Spain.
Myofibrillar myopathy Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Myofibrillar myopathy that also includes the following genes: TPM3 MYOT TTN DNAJB6 LDB3 TRIM32 CRYAB DES FHL1 FLNC
More info about this panel Spain.
Limb-Girdle Muscular Dystrophy Type 1B: LMNA Full Gene Sequencing Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics
This panel specifically test the LMNA gene.
More info about this panel United States.
Limb-Girdle Muscular Dystrophy Type 1B: LMNA Gene Deletion/Duplication Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics
This panel specifically test the LMNA gene.
More info about this panel United States.
Congenital Muscular Dystrophy: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Congenital Muscular Dystrophy: Deletion/Duplication Panel that also includes the following genes: RYR1 TCAP RXYLT1 SELENON FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2
More info about this panel United States.
Dilated Cardiomyopathy: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Dilated Cardiomyopathy: Sequencing Panel that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panel United States.
Neuromuscular Disorders: Gene Sequencing and Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Neuromuscular Disorders: Gene Sequencing and Deletion/Duplication Panel that also includes the following genes: RYR1 RYR2 SGCA SGCB SGCD SGCE SGCG TCAP TNNI2 TNNT1
More info about this panel United States.
Endocrine Disorders: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Endocrine Disorders: Sequencing Panel that also includes the following genes: BLK BMP15 SLC2A2 TAC3 TACR3 HNF1A HNF1B KLF11 WFS1 ZMPSTE24
More info about this panel United States.
Expanded Neuromuscular Disorders: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Expanded Neuromuscular Disorders: Sequencing Panel that also includes the following genes: RYR1 RYR2 BIN1 SCN4A SGCA SGCB SGCD SGCE SGCG TCAP
More info about this panel United States.
Hereditary Neuropathies: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Hereditary Neuropathies: Sequencing Panel that also includes the following genes: SACS SCN9A SLC12A6 SLC1A3 SPG11 ATL1 SPAST SPG7 SPTBN2 SPTLC1
More info about this panel United States.
Limb-Girdle Muscular Dystrophy: Sequencing and Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Limb-Girdle Muscular Dystrophy: Sequencing and Deletion/Duplication Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN VCP CAPN3 CAV3
More info about this panel United States.
Osteogenesis Imperfecta and Decreased Bone Density: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Osteogenesis Imperfecta and Decreased Bone Density: Sequencing Panel that also includes the following genes: TNFRSF11A TYROBP ZMPSTE24 CASR SERPINH1 ANKH IFITM5 SP7 TREM2 FKBP10
More info about this panel United States.
Skeletal Dysplasia: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Skeletal Dysplasia: Sequencing Panel that also includes the following genes: ROR2 RUNX2 SALL1 BMP2 BMPR1B FBXW4 SHH SHOX SLC25A12 SLC26A2
More info about this panel United States.
Comprehensive Cardiovascular: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Comprehensive Cardiovascular: Sequencing Panel that also includes the following genes: RIT1 RYR2 SCN1B SCN4B SCN5A BMPR2 SGCD SKI SLC22A5 BRAF
More info about this panel United States.
Cardiomyopathy: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Cardiomyopathy: Deletion/Duplication Panel that also includes the following genes: RIT1 RYR2 SCN5A SGCD BRAF SOS1 TAZ TCAP TNNC1 TNNI3
More info about this panel United States.
Cardiomyopathy: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Cardiomyopathy: Sequencing Panel that also includes the following genes: RIT1 RYR2 SCN5A SGCD SLC22A5 BRAF SOS1 TAZ TCAP TNNC1
More info about this panel United States.
Comprehensive Cardiovascular: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Comprehensive Cardiovascular: Deletion/Duplication Panel that also includes the following genes: RIT1 RYR2 SCN1B SCN4B SCN5A BMPR2 SGCD SKI BRAF SNTA1
More info about this panel United States.
Congenital Muscular Dystrophy: Sequencing Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Congenital Muscular Dystrophy: Sequencing Panel that also includes the following genes: RYR1 TCAP RXYLT1 SELENON FKRP POMGNT1 CHKB POMT2 COL6A1 COL6A2
More info about this panel United States.
Dilated Cardiomyopathy: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Dilated Cardiomyopathy: Deletion/Duplication Panel that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panel United States.
Endocrine Disorders: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Endocrine Disorders: Deletion/Duplication Panel that also includes the following genes: BLK BMP15 SLC2A2 TAC3 TACR3 HNF1A HNF1B KLF11 WFS1 ZMPSTE24
More info about this panel United States.
Expanded Neuromuscular Disorders: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Expanded Neuromuscular Disorders: Deletion/Duplication Panel that also includes the following genes: RYR1 RYR2 BIN1 SCN4A SGCA SGCB SGCD SGCE SGCG TCAP
More info about this panel United States.
Hereditary Neuropathies: Deletion/Duplication Panel Panel
United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Hereditary Neuropathies: Deletion/Duplication Panel that also includes the following genes: SACS SCN9A SLC12A6 SLC1A3 SPG11 ATL1 SPAST SPG7 SPTBN2 SPTLC1
More info about this panel United States.
Familial Cardiomyopathy Full Gene Sequencing Panel Panel
United States.
By Integrated Genetics Westborough Integrated Genetics Familial Cardiomyopathy Full Gene Sequencing Panel that also includes the following genes: RYR2 SCN5A SGCD TAZ TCAP TGFB3 TMPO TNNC1 TNNI3 TNNT2
More info about this panel United States.
Muscular Dystrophies NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Muscular Dystrophies NGS Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN MMEL1 CAPN3 DNAJB6
More info about this panel United States.
Arrhythmia NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Arrhythmia NGS Panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SNTA1 TGFB3 CACNA1C CACNA2D1 CACNB2 SLC25A20
More info about this panel United States.
Pan-Cardio NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Pan-Cardio NGS Panel that also includes the following genes: MRPL3 RYR2 SCN1B SCN4B SCN5A SDHA SGCD SNTA1 TAZ TBX1
More info about this panel United States.
Hereditary Neuropathies NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Hereditary Neuropathies NGS Panel that also includes the following genes: SCN9A ATL1 SPTLC2 TTR YARS PRX GDAP1 KIF1B LITAF MFN2
More info about this panel United States.
Atrial Fibrillation NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Atrial Fibrillation NGS Panel that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A HCN4 SCN3B GATA4 GATA6 GJA5
More info about this panel United States.
Lipodystrophy NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Lipodystrophy NGS Panel that also includes the following genes: ZMPSTE24 CAV1 BSCL2 TBC1D4 CIDEC AGPAT2 AKT2 LMNA PPARG CAVIN1
More info about this panel United States.
Neuromuscular NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Neuromuscular NGS Panel that also includes the following genes: RYR1 RYR2 SGCA SGCB SGCD SGCE SGCG TCAP TNNI2 TNNT1
More info about this panel United States.
Sudden Death Syndrome NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Sudden Death Syndrome NGS Panel that also includes the following genes: RYR2 SCN1B SCN4B SCN5A SGCD SLC25A4 SNTA1 TAZ TCAP TGFB3
More info about this panel United States.
Left Ventricular Noncompaction NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Left Ventricular Noncompaction NGS Panel that also includes the following genes: TAZ TNNT2 VCL ACTC1 LDB3 DTNA LMNA MYBPC3 MYH7
More info about this panel United States.
Limb-Girdle Muscular Dystrophy NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Limb-Girdle Muscular Dystrophy NGS Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel United States.
Skeletal Dysplasias NGS panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Skeletal Dysplasias NGS panel that also includes the following genes: ROR2 RUNX2 SALL1 BMP2 BMPR1B FBXW4 SHH SLC25A12 SLC26A2 SMARCAL1
More info about this panel United States.
Charcot Marie Tooth Disease Extended NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Charcot Marie Tooth Disease Extended NGS Panel that also includes the following genes: SCN9A SLC12A6 ATL1 SPTLC1 SPTLC2 TTR PRX WNK1 BSCL2 GDAP1
More info about this panel United States.
Dilated Cardiomyopathy NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Dilated Cardiomyopathy NGS Panel that also includes the following genes: SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL ACTC1
More info about this panel United States.
Hypertrophic Cardiomyopathy NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Hypertrophic Cardiomyopathy NGS Panel that also includes the following genes: RYR2 SCN5A SGCD BRAF SOS1 TAZ TCAP TMPO TNNC1 TNNI3
More info about this panel United States.
LMNA Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the LMNA gene.
More info about this panel United States.
KidneySeq - 264 Genes Panel
United States.
By Iowa Institute of Human Genetics University of Iowa KidneySeq - 264 Genes that also includes the following genes: ROBO2 CNNM2 SALL1 ATXN10 SCNN1A SCNN1B SCNN1G SDCCAG8 BMP4 SEMA3E
More info about this panel United States.
Progeria and Progeroid Syndromes Panel Panel
Finland.
By Blueprint Genetics Progeria and Progeroid Syndromes Panel that also includes the following genes: BLM WRN ZMPSTE24 BSCL2 COL3A1 GORAB AGPAT2 ERCC2 ERCC4 ERCC5
More info about this panel Finland.
Atrial Fibrillation Panel Panel
Finland.
By Blueprint Genetics Atrial Fibrillation Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN5A TBX5 CACNB2 LDB3 HCN4 SCN3B GATA6
More info about this panel Finland.
Cardiomyopathy Panel Panel
Finland.
By Blueprint Genetics Cardiomyopathy Panel that also includes the following genes: RIT1 RRAS RYR2 SCN5A SCNN1B SCNN1G SCO2 SDHA SGCA SGCB
More info about this panel Finland.
Emery-Dreifuss Muscular Dystrophy Panel Panel
Finland.
By Blueprint Genetics Emery-Dreifuss Muscular Dystrophy Panel that also includes the following genes: TTN TMEM43 DMD EMD FHL1 LMNA
More info about this panel Finland.
LGMD and Congenital Muscular Dystrophy Panel Panel
Finland.
By Blueprint Genetics LGMD and Congenital Muscular Dystrophy Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Finland.
Comprehensive Muscular Dystrophy / Myopathy Panel Panel
Finland.
By Blueprint Genetics Comprehensive Muscular Dystrophy / Myopathy Panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP TNNT1 TPM2 TPM3 MYOT TTN
More info about this panel Finland.
Charcot-Marie-Tooth Neuropathy Panel Panel
Finland.
By Blueprint Genetics Charcot-Marie-Tooth Neuropathy Panel that also includes the following genes: SACS SBF1 SCN11A SCN9A DST SLC12A6 SPG11 ATL1 SPTLC1 SPTLC2
More info about this panel Finland.
Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel Panel
Finland.
By Blueprint Genetics Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel that also includes the following genes: RYR2 SCN5A TCAP TNNT2 TPM1 TTN VCL JPH2 FBXO32 HCN4
More info about this panel Finland.
Arrhythmia Panel Panel
Finland.
By Blueprint Genetics Arrhythmia Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN5A TBX5 TGFB3 TNNI3 TNNT2 TRDN TTN
More info about this panel Finland.
Premature Ovarian Failure Panel Panel
Finland.
By Blueprint Genetics Premature Ovarian Failure Panel that also includes the following genes: BMP15 FOXL2 STAR WT1 NOBOX CYP17A1 CYP19A1 FSHR GALT GNAS
More info about this panel Finland.
Comprehensive Cardiology Panel Panel
Finland.
By Blueprint Genetics Comprehensive Cardiology Panel that also includes the following genes: RIT1 RRAS RYR2 SCN10A SCN1B SCN5A SCNN1B SCNN1G SCO2 SDHA
More info about this panel Finland.
Comprehensive Metabolism Panel Panel
Finland.
By Blueprint Genetics Comprehensive Metabolism Panel that also includes the following genes: BCS1L CNNM2 RYR1 CNNM4 SCN4A SEC23B SGSH SI SLC40A1 SLC12A3
More info about this panel Finland.
Congenital and Familial Lipodystrophy Panel Panel
Finland.
By Blueprint Genetics Congenital and Familial Lipodystrophy Panel that also includes the following genes: ZMPSTE24 CAV1 BSCL2 TBC1D4 AGPAT2 AKT2 LIPE LMNA PLIN1 PPARG
More info about this panel Finland.
Comprehensive Skeletal Dysplasias and Disorders Panel Panel
Finland.
By Blueprint Genetics Comprehensive Skeletal Dysplasias and Disorders Panel that also includes the following genes: RMRP ROR2 BGN RUNX2 BMP1 BMP2 BMPR1B SF3B4 SH3BP2 SHOX
More info about this panel Finland.
Dilated Cardiomyopathy (DCM) Panel Panel
Finland.
By Blueprint Genetics Dilated Cardiomyopathy (DCM) Panel that also includes the following genes: SCN5A TAZ TBX20 TBX5 TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel Finland.
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel Panel
Finland.
By Blueprint Genetics Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel that also includes the following genes: RYR2 TGFB3 TTN LDB3 CDH2 CTNNA3 DES TMEM43 DSC2 DSG2
More info about this panel Finland.
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel Panel
Finland.
By Blueprint Genetics Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel that also includes the following genes: RIT1 RMRP BCS1L ROR2 BGN RRAS RUNX2 BMP1 BMP2 SEC24D
More info about this panel Finland.
LMNA-related disorders (LMNA) sequencing Panel
Iran.
By Genomic Research Center Shahid Beheshti University of Medical Sciences
This panel specifically test the LMNA gene.
More info about this panel Iran.
Lamin A/C full sequence Panel
Spain.
By Bioarray
This panel specifically test the LMNA gene.
More info about this panel Spain.
Cardiomyopathy, dilated type 1A Panel
Spain.
By Bioarray
This panel specifically test the LMNA gene.
More info about this panel Spain.
Charcot-Marie-Tooth neuropathy type 2B1 Panel
Spain.
By Bioarray
This panel specifically test the LMNA gene.
More info about this panel Spain.
Autosomal dominant limb-girdle muscular dystrophy type 1B Panel
Spain.
By Bioarray
This panel specifically test the LMNA gene.
More info about this panel Spain.
Emery-Dreifuss muscular dystrophy autosomal dominant Panel
Spain.
By Bioarray
This panel specifically test the LMNA gene.
More info about this panel Spain.
CardioGene Set Panel
United States.
By Genomics and Pathology Services Washington University in St. Louis CardioGene Set that also includes the following genes: RIT1 RYR2 SCN1B SCN4B SCN5A SGCD BRAF SNTA1 SOS1 TAZ
More info about this panel United States.
Cardiomyopathy Gene Set Panel
United States.
By Genomics and Pathology Services Washington University in St. Louis Cardiomyopathy Gene Set that also includes the following genes: RIT1 RYR2 SCN5A SGCD BRAF SOS1 TAZ TCAP TMPO TNNC1
More info about this panel United States.
Dilated Cardiomyopathy Gene Set Panel
United States.
By Genomics and Pathology Services Washington University in St. Louis Dilated Cardiomyopathy Gene Set that also includes the following genes: SCN5A SGCD TAZ TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1 TTN
More info about this panel United States.
Left Ventricular Noncompaction Gene Set Panel
United States.
By Genomics and Pathology Services Washington University in St. Louis Left Ventricular Noncompaction Gene Set that also includes the following genes: TAZ TNNT2 VCL ACTC1 CASQ2 LDB3 DTNA LMNA MYBPC3 MYH7
More info about this panel United States.
Noncompaction Cardiomyopathy NGS and Deletion/Duplication Panel Panel
United States.
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children Noncompaction Cardiomyopathy NGS and Deletion/Duplication Panel that also includes the following genes: TNNT2 TPM1 ACTC1 LDB3 DTNA LMNA MYBPC3 MYH7
More info about this panel United States.
LMNA Gene Sequencing and Deletion/Duplication Analysis Panel
United States.
By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
This panel specifically test the LMNA gene.
More info about this panel United States.
Comprehensive Cardiomyopathy Panel Panel
United States.
By ApolloGen, Inc. Comprehensive Cardiomyopathy Panel that also includes the following genes: SCN5A BMPR2 SGCD TAZ TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1
More info about this panel United States.
Dilated Cardiomyopathy Panel Panel
United States.
By ApolloGen, Inc. Dilated Cardiomyopathy Panel that also includes the following genes: SCN5A SGCD TAZ TCAP TMPO TNNI3 TNNT2 TPM1 VCL ACTC1
More info about this panel United States.
iGene Cardiac Panel Panel
United States.
By ApolloGen, Inc. iGene Cardiac Panel that also includes the following genes: RYR2 SCN5A TNNI3 TNNT2 TPM1 TTN ACTC1 PCSK9 COL3A1 DSG2
More info about this panel United States.
Cardiomyopathy Exome Panel Panel
United States.
By Northwest Clinical Genomics Laboratory University of Washington Cardiomyopathy Exome Panel that also includes the following genes: RIT1 RYR2 SCN5A SGCD BRAF SOS1 TAZ TCAP TMPO TNNC1
More info about this panel United States.
Cardiac Arrhythmia Exome Panel Panel
United States.
By Northwest Clinical Genomics Laboratory University of Washington Cardiac Arrhythmia Exome Panel that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SNTA1 TNNT2 TRDN TTN CACNA1C
More info about this panel United States.
LMNA-related disorders (LMNA) sequencing Panel
Iran.
By Center for Comprehensive Genetic Services Shahid Beheshti University of Medical Sciences
This panel specifically test the LMNA gene.
More info about this panel Iran.
Familial Dilated Cardiomyopathy Panel by NGS Panel
Canada.
By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Familial Dilated Cardiomyopathy Panel by NGS that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL
More info about this panel Canada.
Left Ventricular Noncompaction Panel by NGS Panel
Canada.
By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Left Ventricular Noncompaction Panel by NGS that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN VCL
More info about this panel Canada.
LMNA Gene, entire coding region or targeted variant Panel
Canada.
By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute
This panel specifically test the LMNA gene.
More info about this panel Canada.
Arrhythmogenic Right Ventricular Cardiomyopathy Panel by NGS Panel
Canada.
By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Arrhythmogenic Right Ventricular Cardiomyopathy Panel by NGS that also includes the following genes: RYR2 SCN5A TGFB3 TTN DES TMEM43 DSC2 DSG2 DSP JUP
More info about this panel Canada.
Cardiomyopathies Panel
Italy.
By Cardiovascular Genetics PO San Francesco-NUORO (IT) Cardiomyopathies that also includes the following genes: TAZ TNNI3 TNNT2 TTN TTR LMNA MYBPC3 MYH6 MYH7 MYL2
More info about this panel Italy.
CHARCOT-MARIE-TOOTH DISEASE TYPE 2B1 Panel
Spain.
By Laboratorio de Genetica Clinica SL
This panel specifically test the LMNA gene.
More info about this panel Spain.
LIPODYSTROPHY, FAMILIAL PARTIAL Panel
Spain.
By Laboratorio de Genetica Clinica SL LIPODYSTROPHY, FAMILIAL PARTIAL that also includes the following genes: LMNA PPARG
More info about this panel Spain.
FAMILIAL DILATED CARDIOMYOPATHY Panel
Spain.
By Laboratorio de Genetica Clinica SL FAMILIAL DILATED CARDIOMYOPATHY that also includes the following genes: SCN5A TCAP TMPO TNNC1 TNNI3 TNNT2 TPM1 TTN VCL ACTC1
More info about this panel Spain.
FAMILIAL DILATED CARDIOMYOPATHY/HYPERTROPHIC/NONCOMPACTION: NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL FAMILIAL DILATED CARDIOMYOPATHY/HYPERTROPHIC/NONCOMPACTION: NGS PANEL that also includes the following genes: MRPL3 SCN5A SGCD TAZ TBX20 TBX5 TCAP TNNC1 TNNI3 TNNT2
More info about this panel Spain.
FAMILIAL ISOLATED ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA: NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL FAMILIAL ISOLATED ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA: NGS PANEL that also includes the following genes: RYR2 TGFB3 CTNNA3 DES TMEM43 DSC2 DSG2 DSP JUP LMNA
More info about this panel Spain.
DILATED CARDIOMYOPATHY WITH ISOLATED NONCOMPACTION OF LEFT VENTRICULAR Panel
Spain.
By Laboratorio de Genetica Clinica SL DILATED CARDIOMYOPATHY WITH ISOLATED NONCOMPACTION OF LEFT VENTRICULAR that also includes the following genes: TAZ LDB3 DTNA LMNA MYBPC3 MYH7
More info about this panel Spain.
CHARCOT-MARIE-TOOTH : NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL CHARCOT-MARIE-TOOTH : NGS PANEL that also includes the following genes: YARS PRX BSCL2 GDAP1 KIF1B LITAF FIG4 MFN2 TRPV4 FGD4
More info about this panel Spain.
MUSCULAR DYSTROPHY, EMERY-DREYFUSS, TYPE 2 & TYPE 3 Panel
Spain.
By Laboratorio de Genetica Clinica SL
This panel specifically test the LMNA gene.
More info about this panel Spain.
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (AUT. DOMINANT) (LAMIN A/C DEFICIENCY) Panel
Spain.
By Laboratorio de Genetica Clinica SL
This panel specifically test the LMNA gene.
More info about this panel Spain.
MUSCULAR DYSTROPHY, LIMB-GIRDLE:NGS NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL MUSCULAR DYSTROPHY, LIMB-GIRDLE:NGS NGS PANEL that also includes the following genes: SGCA SGCB SGCD SGCG BVES TCAP MYOT TTN CAPN3 DNAJB6
More info about this panel Spain.
FAMILIAL DILATED CARDIOMYOPATHY, NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL FAMILIAL DILATED CARDIOMYOPATHY, NGS PANEL that also includes the following genes: SCN5A SGCD TAZ TBX20 TBX5 TCAP TMPO TNNC1 TNNI3 TPM1
More info about this panel Spain.
CARDIOMYOPATHY WITH ISOLATED NONCOMPACTION OF LEFT VENTRICULAR: NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL CARDIOMYOPATHY WITH ISOLATED NONCOMPACTION OF LEFT VENTRICULAR: NGS PANEL that also includes the following genes: TAZ TNNT2 TPM1 PRDM16 ACTC1 LDB3 ACTN2 HCN4 MIB1 CSRP3
More info about this panel Spain.
Charcot-Marie-Tooth neuropathy axonal autosomal dominant panel Panel
Canada.
By LifeLabs Genetics Charcot-Marie-Tooth neuropathy axonal autosomal dominant panel that also includes the following genes: SLC12A6 YARS ARHGEF10 GDAP1 KIF1B MFN2 TRPV4 AARS MED25 DYNC1H1
More info about this panel Canada.
Limb-girdle muscular dystrophy panel Panel
Canada.
By LifeLabs Genetics Limb-girdle muscular dystrophy panel that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Canada.
Autosomal Dominant Enery-Dreifuss Muscular Dystrophy Type 2 , Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Autosomal Recessive Emery-Dreifuss Muscular Dystrophy Type 3, Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Charcot-Marie-Tooth Disease Type 2B1, Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Limb-Girdle Muscular Dystrophy Type 1B, Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Hutchinson-Gilford Progeria Syndrome , Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated Cardiomyopathy, Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Familial Partial Lipodystrophy Type Dunnigan, Sequencing LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Dilated Cardiomyopathy , Deletions-Duplications (MLPA) LMNA Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the LMNA gene.
More info about this panel Spain.
Autosomal Dominant Limb-Girdle Muscular Dystrophy, Panel Massive Sequencing (NGS) 3 Genes Panel
Spain.
By Reference Laboratory Genetics Autosomal Dominant Limb-Girdle Muscular Dystrophy, Panel Massive Sequencing (NGS) 3 Genes that also includes the following genes: MYOT CAV3 LMNA
More info about this panel Spain.
Dilated Cardiomyopathy, Panel Massive Sequencing (NGS) 30 Genes Panel
Spain.
By Reference Laboratory Genetics Dilated Cardiomyopathy, Panel Massive Sequencing (NGS) 30 Genes that also includes the following genes: SCN5A SGCD TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1 TTN TTR
More info about this panel Spain.
Hereditary Peripheral Neuropathy , Panel Massive Sequencing (NGS) 31 Genes Panel
Spain.
By Reference Laboratory Genetics Hereditary Peripheral Neuropathy , Panel Massive Sequencing (NGS) 31 Genes that also includes the following genes: SLC12A6 YARS PRX GDAP1 KIF1B LITAF FIG4 MFN2 TRPV4 FGD4
More info about this panel Spain.
Limb-Girdle Muscular Distrophy , Panel Massive Sequencing (NGS) 22 Genes Panel
Spain.
By Reference Laboratory Genetics Limb-Girdle Muscular Distrophy , Panel Massive Sequencing (NGS) 22 Genes that also includes the following genes: SGCA SGCB SGCD SGCG TCAP MYOT TTN CAPN3 DNAJB6 CAV3
More info about this panel Spain.
Charcot-Marie-Tooth Disease, Panel Massive Sequencing (NGS) 32 Genes Panel
Spain.
By Reference Laboratory Genetics Charcot-Marie-Tooth Disease, Panel Massive Sequencing (NGS) 32 Genes that also includes the following genes: YARS PRX BSCL2 GDAP1 KIF1B LITAF FIG4 MFN2 TRPV4 FGD4
More info about this panel Spain.
Catecholaminergic Polymorphic Ventricular Tachycardia , Panel Massive Sequencing (NGS) 14 Genes Panel
Spain.
By Reference Laboratory Genetics Catecholaminergic Polymorphic Ventricular Tachycardia , Panel Massive Sequencing (NGS) 14 Genes that also includes the following genes: RYR2 TAZ TNNT2 TPM1 VCL ACTC1 CASQ2 LDB3 HCN4 DNAJC19
More info about this panel Spain.
Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes Panel
Spain.
By Reference Laboratory Genetics Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes that also includes the following genes: RYR2 SCN10A SCN1B SCN2B SCN4B SCN5A SNTA1 TGFB3 TNNC1 TNNI3
More info about this panel Spain.
Muscle Polyneuropathies , Panel Massive Sequencing (NGS) 111 Genes Panel
Spain.
By Reference Laboratory Genetics Muscle Polyneuropathies , Panel Massive Sequencing (NGS) 111 Genes that also includes the following genes: RYR1 RYR2 BIN1 SCN4A SGCA SGCB SGCD SGCE SGCG TCAP
More info about this panel Spain.
Lipodystrophy Related Disorders , Panel Massive Sequencing (NGS) 10 Genes Panel
Spain.
By Reference Laboratory Genetics Lipodystrophy Related Disorders , Panel Massive Sequencing (NGS) 10 Genes that also includes the following genes: ZMPSTE24 CAV1 BSCL2 CIDEC AGPAT2 LMNA LMNB2 PLIN1 PPARG CAVIN1
More info about this panel Spain.
Charcot-Marie-Tooth Disease Type 2 , Panel Massive Sequencing (NGS) 20 Genes Panel
Spain.
By Reference Laboratory Genetics Charcot-Marie-Tooth Disease Type 2 , Panel Massive Sequencing (NGS) 20 Genes that also includes the following genes: GDAP1 KIF1B MFN2 TRPV4 AARS LRSAM1 MED25 DYNC1H1 DNM2 HSPB8
More info about this panel Spain.
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes Panel
Spain.
By Reference Laboratory Genetics Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SGCD SLC25A3 SLC6A4 SNTA1 TAZ
More info about this panel Spain.
Cardiac Conduction System Related Disorders , Panel Massive Sequencing (NGS) 20 Genes Panel
Spain.
By Reference Laboratory Genetics Cardiac Conduction System Related Disorders , Panel Massive Sequencing (NGS) 20 Genes that also includes the following genes: SCN10A SCN1B SCN5A TBX5 TTR CACNA1D ACTC1 HCN4 TRPM4 TNNI3K
More info about this panel Spain.
Emery-Dreifuss Muscular Dystrophy , Panel Massive Sequencing (NGS) 6 Genes Panel
Spain.
By Reference Laboratory Genetics Emery-Dreifuss Muscular Dystrophy , Panel Massive Sequencing (NGS) 6 Genes that also includes the following genes: SYNE2 SYNE1 TMEM43 EMD FHL1 LMNA
More info about this panel Spain.
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Panel (ARVD/ARVC Panel) Panel
Germany.
By Labor Dr. Wisplinghoff Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Panel (ARVD/ARVC Panel) that also includes the following genes: RYR2 TGFB3 TTN DES TMEM43 DSC2 DSG2 DSP JUP LMNA
More info about this panel Germany.
Phosphorus Dilated Cardiomyopathy Including Recessive Pediatric Syndromes Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Dilated Cardiomyopathy Including Recessive Pediatric Syndromes Panel that also includes the following genes: RYR2 SCN5A SDHA SGCD SLC22A5 TAZ TCAP TNNC1 TNNI3 TNNT2
More info about this panel United States.
Phosphorus Pan Arrhythmia Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Arrhythmia Panel that also includes the following genes: RYR2 SCN10A SCN4B SCN5A SNTA1 TGFB3 TNNI3 TNNT2 TRDN TTN
More info about this panel United States.
Phosphorus Pan Cardiomyopathy Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A SGCD SLC22A5 TAZ TCAP TGFB3 TNNC1 TNNI3 TNNT2
More info about this panel United States.
Phosphorus Pan Cardiomyopathy Including Recessive Pediatric Syndromes Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Cardiomyopathy Including Recessive Pediatric Syndromes Panel that also includes the following genes: RIT1 RRAS RYR2 SCN5A SDHA SGCD SLC22A5 BRAF SOS1 SOS2
More info about this panel United States.
Phosphorus Pan Cardiomyopathy Including Rasopathies Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Cardiomyopathy Including Rasopathies Panel that also includes the following genes: RIT1 RRAS RYR2 SCN5A SGCD SLC22A5 BRAF SOS1 SOS2 TAZ
More info about this panel United States.
Phosphorus Pan Arrhythmia and Cardiomyopathy Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Arrhythmia and Cardiomyopathy Panel that also includes the following genes: RYR2 SCN10A SCN4B SCN5A SGCD SLC22A5 SNTA1 TAZ TCAP TGFB3
More info about this panel United States.
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies Panel that also includes the following genes: RIT1 RRAS RYR2 SCN10A SCN4B SCN5A SGCD SLC22A5 BRAF SNTA1
More info about this panel United States.
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel that also includes the following genes: RIT1 RRAS RYR2 SCN10A SCN4B SCN5A SDHA SGCD SLC22A5 BRAF
More info about this panel United States.
Phosphorus Pan Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel that also includes the following genes: RIT1 RRAS RYR2 SCN5A SDHA SGCD SLC22A5 BRAF SOS1 SOS2
More info about this panel United States.
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Recessive Pediatric Syndromes Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Pan Arrhythmia and Cardiomyopathy Including Recessive Pediatric Syndromes Panel that also includes the following genes: RYR2 SCN10A SCN4B SCN5A SDHA SGCD SLC22A5 SNTA1 TAZ TCAP
More info about this panel United States.
Phosphorus Arrhythmogenic Cardiomyopathy Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Arrhythmogenic Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A TGFB3 TNNI3 TNNT2 TTN LDB3 ACTN2 RBM20 DES
More info about this panel United States.
Phosphorus Dilated Cardiomyopathy Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Dilated Cardiomyopathy Panel that also includes the following genes: RYR2 SCN5A SGCD SLC22A5 TAZ TCAP TNNC1 TNNI3 TNNT2 TPM1
More info about this panel United States.
Phosphorus Left Ventricular Noncompaction Panel Panel
United States.
By Phosphorus Diagnostics LLC Phosphorus Left Ventricular Noncompaction Panel that also includes the following genes: RYR2 SCN5A TAZ TNNI3 TNNT2 TPM1 VCL ACTC1 LDB3 ACTN2
More info about this panel United States.
Tempus xT assay Panel
United States.
By Tempus Labs, Inc. Tempus xT assay that also includes the following genes: BCL6 RIT1 BCL7A BCR ROS1 RPL5 RPS15 RPS6KB1 RUNX1 RXRA
More info about this panel United States.
Tempus xO assay Panel
United States.
By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2
More info about this panel United States.
Hutchinson-Gilford Progeria Syndrome: targeted gene sequencing Panel
Canada.
By CEN4GEN Institute for Genomics and Molecular Diagnostics
This panel specifically test the LMNA gene.
More info about this panel Canada.
LMNA-Related Dilated Cardiomyopathy: gene sequencing Panel
Canada.
By CEN4GEN Institute for Genomics and Molecular Diagnostics
This panel specifically test the LMNA gene.
More info about this panel Canada.
Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis Panel
Canada.
By CEN4GEN Institute for Genomics and Molecular Diagnostics Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis that also includes the following genes: BMP15 FOXL2 POF1B PSMC3IP HFM1 NOBOX FIGLA CYP17A1 CYP19A1 DIAPH2
More info about this panel Canada.
Emery-Dreifuss Muscular Dystrophy: gene sequencing panel Panel
Canada.
By CEN4GEN Institute for Genomics and Molecular Diagnostics Emery-Dreifuss Muscular Dystrophy: gene sequencing panel that also includes the following genes: EMD FHL1 LMNA
More info about this panel Canada.
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