Neuroblastoma, Susceptibility To, 2; Nblst2

Clinical Features

Top most frequent phenotypes and symptoms related to Neuroblastoma, Susceptibility To, 2; Nblst2

  • Seizures
  • Neoplasm
  • Arrhythmia
  • Hyperhidrosis
  • Aganglionic megacolon
  • Prolonged QT interval
  • Neuroblastoma
  • Abnormal pupil morphology
  • Ganglioneuroma
  • Neoplasm of the nervous system
And another 2 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

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Neuroblastoma, Susceptibility To, 2; Nblst2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Hereditary Brain, CNS, PNS Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, MEN1, ALK, ATM, MRE11, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU
Specificity
6 %
Genes
100 %
Hereditary Brain, CNS, PNS Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, MEN1, ALK, ATM, MRE11, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU
Specificity
6 %
Genes
100 %
Comprehensive Hereditary Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RUNX1, TP53, WT1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127 , (...)

View the complete list with 41 more genes
Specificity
2 %
Genes
100 %
Comprehensive Pulmonary Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

INVS, FBLN5, ELN, DTNBP1, RPGR, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CCDC39, AP3B1, ALMS1, STAT3, CFTR, FOXF1, TINF2, TSC2, TSC1 , (...)

View the complete list with 73 more genes
Specificity
2 %
Genes
100 %
Congenital Central Hypoventilation Syndrome (CCHS) PHOX2B Screening Test.

By Genetics Laboratory - Department of Pathology Rush University Medical Center in United States.

PHOX2B
Specificity
100 %
Genes
100 %
VistaSeq Brain/CNS/PNS Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, RB1, MEN1, ALK, NBN, PTCH1, PHOX2B, NF2, SUFU, NF1, SMARCB1
Specificity
6 %
Genes
100 %
Central Hypoventilation Syndrome Panel (6 Genes).

By Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine) in United States.

RET, PHOX2B, EDN3, BDNF, ASCL1, GDNF
Specificity
17 %
Genes
100 %
PulmoGene Panel (64 Genes).

By Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine) in United States.

FBLN5, RET, ELN, DTNBP1, RPGR, FBN1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CCDC39, AP3B1, STAT3, CFTR, FOXF1, HRAS, TSC2, TSC1 , (...)

View the complete list with 44 more genes
Specificity
2 %
Genes
100 %
Cancer Panel, Hereditary, Sequencing 46 Genes, Deletion/Duplication, 47 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, TP53, RB1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1 , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
100 %
Hereditary Cancer Panel - Neuro17.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, MEN1, TSC2, TSC1, ALK, NBN, PTCH1, PHOX2B, NF2, SUFU, NF1
Specificity
6 %
Genes
100 %
BrainTumorNext.

By Ambry Genetics in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, PTEN, TP53, MEN1, TSC2, TSC1, ALK, NBN, PTCH1, PHOX2B, NF2, SUFU, CDKN2A, PRKAR1A, NF1 , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
100 %
CancerNext-Expanded.

By Ambry Genetics in United States.

BRCA1, BRCA2, VHL, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, TP53, RB1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1, SDHA , (...)

View the complete list with 44 more genes
Specificity
2 %
Genes
100 %
CustomNext: Cancer.

By Ambry Genetics in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, TP53, RB1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1 , (...)

View the complete list with 48 more genes
Specificity
2 %
Genes
100 %
PHOX2B gene sequence.

By Ambry Genetics in United States.

PHOX2B
Specificity
100 %
Genes
100 %
PHOX2B. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PHOX2B
Specificity
100 %
Genes
100 %
Congenital Central Hypoventilation Syndrome - PHOX2B Sequence Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

PHOX2B
Specificity
100 %
Genes
100 %
Congenital Central Hypoventilation Syndrome - PHOX2B Known Point Mutation Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

PHOX2B
Specificity
100 %
Genes
100 %
Neuroblastoma -Sequence Analysis for ALK Ex 21-28 & PHOX2B Ex 1-3.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

ALK, PHOX2B
Specificity
50 %
Genes
100 %
CHOP Comprehensive Hereditary Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

BRCA1, BRCA2, HFE, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, ABCB11, RB1, SDHAF2, RET, SLC25A13, SDHC, FH , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
100 %
Hereditary Brain Tumor Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, MEN1, ALK, ATM, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU, SMARCB1
Specificity
6 %
Genes
100 %
Congenital Central Hypoventilation Syndrome (Ondine Curse) (sequence analysis of PHOX2B gene).

By CGC Genetics in Portugal.

PHOX2B
Specificity
100 %
Genes
100 %
Ondine syndrome (deletion/duplication analysis of PHOX2B gene).

By CGC Genetics in Portugal.

PHOX2B
Specificity
100 %
Genes
100 %
OncoRisk (NGS panel for 48 genes).

By CGC Genetics in Portugal.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH, SDHB, MEN1 , (...)

View the complete list with 28 more genes
Specificity
3 %
Genes
100 %
OncoRisk Plus (NGS panel for 89 genes).

By CGC Genetics in Portugal.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
Hereditary Neuroblastoma and congenital Central Hypoventilation Syndrome via the PHOX2B Gene.

By PreventionGenetics PreventionGenetics in United States.

PHOX2B
Specificity
100 %
Genes
100 %
Congenital Central Hypoventilation Syndrome (CCHS) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

RET, PHOX2A, PHOX2B, EDN3, BDNF, ASCL1, BMP2
Specificity
15 %
Genes
100 %
Neuroblastoma Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KIF1B, ALK, PHOX2B
Specificity
34 %
Genes
100 %
Congenital Central Hypoventilation Syndrome.

By MGZ Medical Genetics Center in Germany.

PHOX2B
Specificity
100 %
Genes
100 %
Hereditary Cancer Syndromes - panels.

By MGZ Medical Genetics Center in Germany.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, RB1, SDHAF2, RET, SDHC , (...)

View the complete list with 80 more genes
Specificity
1 %
Genes
100 %
Newborn: Neonatal Apneas.

By MGZ Medical Genetics Center in Germany.

CHAT, PHOX2B, CHRNE, RAPSN, SCN4A, COLQ, CHRNA1, CHRND, CHRNB1, LAS1L, GLRB, GLRA1, SLC6A5
Specificity
8 %
Genes
100 %
Muscle Weakness (Myopathy, Muscular Dystrophy).

By MGZ Medical Genetics Center in Germany.

TTR, ACAD9, ACADM, ACADS, AGL, ACADVL, TWNK, GAA, TUBB3, AMACR, CPT2, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, MFN2, CRYAB, HADHA , (...)

View the complete list with 159 more genes
Specificity
1 %
Genes
100 %
Central hypoventilation syndrome, congenital, with or without Hirschsprung disease.

By Centogene AG - the Rare Disease Company in Germany.

PHOX2B
Specificity
100 %
Genes
100 %
Central hypoventilation syndrome, congenital, with or without Hirschsprung disease.

By Centogene AG - the Rare Disease Company in Germany.

PHOX2B
Specificity
100 %
Genes
100 %
Central hypoventilation syndrome, congenital, with or without Hirschsprung disease.

By Centogene AG - the Rare Disease Company in Germany.

PHOX2B
Specificity
100 %
Genes
100 %
Central hypoventilation syndrome with or without Hirschsprung disease.

By Centogene AG - the Rare Disease Company in Germany.

PHOX2B
Specificity
100 %
Genes
100 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
100 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company in Germany.

BRCA2, F2, F5, MTHFR, UBE3A, MCCC1, MCCC2, AARS2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
100 %
CentoICU platinum.

By Centogene AG - the Rare Disease Company in Germany.

BRCA2, F2, F5, MTHFR, UBE3A, MCCC1, MCCC2, AARS2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
100 %
Comprehensive pulmonary disease panel.

By Centogene AG - the Rare Disease Company in Germany.

FBLN5, RET, ELN, DTNBP1, FBN1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CCDC39, AP3B1, STAT3, CFTR, FOXF1, TINF2, TSC2, TSC1, PHOX2B , (...)

View the complete list with 46 more genes
Specificity
2 %
Genes
100 %
PHOX2B deletion/duplication testing.

By Molecular Diagnostics Ann and Robert H. Lurie Children's Hospital of Chicago in United States.

PHOX2B
Specificity
100 %
Genes
100 %
PHOX2B sequencing of the entire coding sequence and splice sites.

By Molecular Diagnostics Ann and Robert H. Lurie Children's Hospital of Chicago in United States.

PHOX2B
Specificity
100 %
Genes
100 %
Cancer Predisposition.

By Asper Biogene Asper Biogene LLC in Estonia.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, RB1, SDHAF2, RET, SDHC, FH , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
100 %
Congenital central hypoventilation syndrome (CCHS), PHOX2B sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

PHOX2B
Specificity
100 %
Genes
100 %
Invitae Multi-Cancer Panel.

By Invitae in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH , (...)

View the complete list with 60 more genes
Specificity
2 %
Genes
100 %
Invitae Nervous System/Brain Cancer Panel.

By Invitae in United States.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, TP53, RB1, MEN1, HRAS, TSC2, TSC1, ALK, PTCH1, PHOX2B, NF2, SUFU, PRKAR1A , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
100 %
Invitae Pediatric Nervous System/Brain Tumors Panel.

By Invitae in United States.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, TP53, RB1, MEN1, HRAS, TSC2, TSC1, ALK, PTCH1, PHOX2B, NF2, SUFU, PRKAR1A , (...)

View the complete list with 4 more genes
Specificity
5 %
Genes
100 %
Invitae Familial Neuroblastoma Panel.

By Invitae in United States.

ALK, PHOX2B
Specificity
50 %
Genes
100 %
Invitae Pediatric Solid Tumors Panel.

By Invitae in United States.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, RECQL4, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1, SDHA , (...)

View the complete list with 28 more genes
Specificity
3 %
Genes
100 %
Ondine syndrome: PHOX2B gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PHOX2B
Specificity
100 %
Genes
100 %
Ondine syndrome: Poly-Ala expansion PHOX2B gene.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PHOX2B
Specificity
100 %
Genes
100 %
Congenital Central Hypoventilation Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

RET, PHOX2B, EDN3, HOXA1, BDNF, ASCL1, GDNF
Specificity
15 %
Genes
100 %
Pulmonary Disease: Comprehensive Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

FBLN5, RET, ELN, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CCDC39, AP3B1, STAT3, CFTR, TSC2, TSC1, PHOX2B, FLCN, ENG, SERPINA1 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
100 %
Hereditary Cancer Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, TP53, WT1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1, BLM , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
100 %
Brain, CNS, and PNS Cancer: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, MEN1, ALK, ATM, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU
Specificity
7 %
Genes
100 %
Brain, CNS, and PNS Cancer: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VHL, APC, MSH2, MSH6, MLH1, TP53, MEN1, ALK, ATM, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU
Specificity
7 %
Genes
100 %
Congenital Central Hypoventilation Syndrome: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

RET, PHOX2B, EDN3, HOXA1, BDNF, ASCL1, GDNF
Specificity
15 %
Genes
100 %
Hereditary Cancer Syndrome: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, MSH6, MLH1, MUTYH, PTEN, TP53, WT1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1, BLM , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
100 %
Hypoventilation Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

PHOX2B, EDN3, BDNF, ASCL1, GDNF
Specificity
20 %
Genes
100 %
Lung Disorders NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

FBLN5, RET, ELN, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CCDC39, AP3B1, CFTR, TSC2, TSC1, PHOX2B, FLCN, ENG, SERPINA1, SCNN1A , (...)

View the complete list with 31 more genes
Specificity
2 %
Genes
100 %
Central Hypoventilation Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RET, PHOX2B, EDN3, BDNF, ASCL1, GDNF
Specificity
17 %
Genes
100 %
PHOX2B.

By Fulgent Genetics Fulgent Genetics in United States.

PHOX2B
Specificity
100 %
Genes
100 %
Nervous System / Brain Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, TP53, MEN1, HRAS, TSC2, TSC1, ALK, ATM, PTCH1, PHOX2B, NF2, SUFU, PRKAR1A , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
100 %
Comprehensive Cancer Panel.

By Fulgent Genetics Fulgent Genetics in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, MC1R, TYR , (...)

View the complete list with 104 more genes
Specificity
1 %
Genes
100 %
Hemato-oncology chromosomal microarray.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

BRCA1, BRCA2, APC, MSH2, MLH1, TP53, COL1A1, RB1, BLM, BRAF, HRAS, ALK, PTCH1, PHOX2B, SUFU, CDH1, FUS, SETD2, KDM5C, PAX3 , (...)

View the complete list with 72 more genes
Specificity
2 %
Genes
100 %
Hirschsprung Disease Panel.

By Blueprint Genetics in Finland.

RET, RMRP, PHOX2B, L1CAM, KIF1BP, ZEB2, EDN3, PAX3, EDNRB, SOX10, MITF, BDNF, NRTN, NRG1, CELSR3
Specificity
7 %
Genes
100 %
Hereditary Pediatric Cancer Panel.

By Blueprint Genetics in Finland.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, RECQL4, RUNX1, TP53, WT1, SDHAF2, RET, SDHC, RAF1, FH, SDHB, TMEM127, MEN1 , (...)

View the complete list with 51 more genes
Specificity
2 %
Genes
100 %
Comprehensive Hereditary Cancer Panel.

By Blueprint Genetics in Finland.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, SDHAF2, RET, SDHC, RAF1 , (...)

View the complete list with 126 more genes
Specificity
1 %
Genes
100 %
Central Hypoventilation and Apnea Panel.

By Blueprint Genetics in Finland.

RET, MECP2, CHAT, PHOX2B, CHRNE, RAPSN, SCN4A, COLQ, CHRNA1, CHRND, CHRNB1, ZEB2, EDN3, GLRA1, SLC6A5
Specificity
7 %
Genes
100 %
Comprehensive Pulmonology Panel.

By Blueprint Genetics in Finland.

FBLN5, RET, ELN, SMPD1, MECP2, HPS1, HPS4, CCDC39, CHAT, STAT3, CFTR, FOXF1, TINF2, TSC2, TSC1, PHOX2B, FLCN, CHRNE, SERPINA1, SLC7A7 , (...)

View the complete list with 46 more genes
Specificity
2 %
Genes
100 %
Haddad syndrome.

By Bioarray in Spain.

PHOX2B
Specificity
100 %
Genes
100 %
Caris MI TumorSeek 592-Gene NGS Panel.

By Caris Life Sciences in United States.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, FOXL2, HNF1A, PPARG, COL1A1, WT1, RB1, SDHAF2 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
100 %
HYPOVENTILATION SYNDROME, CONGENITAL CENTRAL (ONDINE SYNDROME).

By Laboratorio de Genetica Clinica SL in Spain.

RET, PHOX2B, EDN3, BDNF, ASCL1, GDNF
Specificity
17 %
Genes
100 %
Ondine Syndrome, Sequencing PHOX2B Gene.

By Reference Laboratory Genetics in Spain.

PHOX2B
Specificity
100 %
Genes
100 %
Ondine Syndrome (Congenital Central Hypoventilation Syndrome) , Deletions-Duplications (MLPA) PHOX2B Gene.

By Reference Laboratory Genetics in Spain.

PHOX2B
Specificity
100 %
Genes
100 %
Oncology Genetic Panel , Panel Massive Sequencing (NGS) 90 Genes.

By Reference Laboratory Genetics in Spain.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, HNF1A, WT1, RB1, SDHAF2, RET, SDHC , (...)

View the complete list with 70 more genes
Specificity
2 %
Genes
100 %
Ondine Syndrome (Congenital Central Hypoventilation Syndrome), Panel Massive Sequencing (NGS) 6 Genes.

By Reference Laboratory Genetics in Spain.

RET, PHOX2B, EDN3, BDNF, ASCL1, GDNF
Specificity
17 %
Genes
100 %
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes.

By Reference Laboratory Genetics in Spain.

TTR, RET, EYA4, PITX2, DSP, CRYAB, DNM1L, SLC25A3, TSFM, DNAJC19, PHOX2A, TAZ, DMD, DMPK, PTPN11, PHOX2B, FKTN, LMNA, CAV3, TTN , (...)

View the complete list with 75 more genes
Specificity
2 %
Genes
100 %
Neuroblastoma , Panel Massive Sequencing (NGS) 4 Genes.

By Reference Laboratory Genetics in Spain.

KIF1B, NME1, ALK, PHOX2B
Specificity
25 %
Genes
100 %
Phosphorus Brain and Nervous System Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, TP53, RB1, SDHAF2, RET, SDHC, SDHB, TMEM127, MEN1, SDHA, HRAS, TSC2, TSC1 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
100 %
Phosphorus Pan-Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH , (...)

View the complete list with 63 more genes
Specificity
2 %
Genes
100 %
Phosphorus Pediatric Cancers Panel.

By Phosphorus Diagnostics LLC in United States.

VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
100 %
Tempus xT assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, MTHFR, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ATP7B, FOXL2, HNF1A, WT1, RB1 , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
100 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ABCB11, ABCB4, FKBP10, FOXL2, HNF1A, PPARG , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
100 %
Brain, CNS, and PNS Cancer: Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

VHL, APC, MSH2, PMS2, MSH6, MLH1, TP53, MEN1, ALK, ATM, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU
Specificity
7 %
Genes
100 %
Brain, CNS, and PNS Cancer: Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

VHL, APC, MSH2, MSH6, MLH1, TP53, MEN1, ALK, ATM, NBN, PTCH1, PHOX2B, NF2, PALB2, SUFU
Specificity
7 %
Genes
100 %
CEN4GEN Comprehensive Hereditary Cancer Syndrome: Gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BRCA1, BRCA2, HFE, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, WT1, RB1, SDHAF2, RET, MC1R , (...)

View the complete list with 123 more genes
Specificity
1 %
Genes
100 %
Hereditary Cancer Syndrome: Gene Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BRCA1, BRCA2, VHL, APC, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, TP53, WT1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1, BLM , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
100 %
Hereditary Cancer Syndrome: Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, MSH6, MLH1, MUTYH, PTEN, TP53, WT1, SDHAF2, RET, SDHC, FH, SDHB, TMEM127, MEN1, BLM , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
100 %

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