NKX3-2 gene related symptoms and diseases
All the information presented here about the NKX3-2 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 NKX3-2 gene
Symptoms // Phenotype | % Cases |
---|---|
Short stature | Very Common - Between 80% and 100% cases |
Disproportionate short stature | Very Common - Between 80% and 100% cases |
Abnormality of the epididymis | Very Common - Between 80% and 100% cases |
Enchondroma | Very Common - Between 80% and 100% cases |
Delayed pubic bone ossification | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NKX3-2 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Enlarged epiphyses
- Pseudoepiphyses
- Abnormally ossified vertebrae
- Stiff neck
- Hypoplastic ilia
- Disproportionate short-trunk short stature
- Protuberant abdomen
- Metaphyseal dysplasia
And 13 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NKX3-2 gene
Here you will find a list of rare diseases related to the NKX3-2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA
Description
Spondylo-megaepiphyseal-metaphyseal dysplasia is a rare, genetic primary bone displasia characterized by disproportionate short stature with short, stiff neck and trunk and relatively long limbs, fingers and toes (which may present flexion contractures), severe vertebral body ossification delay (with frequent kyknodysostosis), markedly enlarged round epiphyses of the long bones, absent ossification of pubic bones and multiple pseudoepiphyses of the short tubular bones in hands and feet. Neurological manifestations resulting from cervical spine instability may be observed.
Most common symptoms of SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA
- Short stature
- Hypertelorism
- Flexion contracture
- Macrocephaly
- Short neck
More info about SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA
Search interest in NKX3-2
Potential gene panels for NKX3-2 gene
NKX3-2 (BAPX1) - Spondylo-megaepiphyseal-metaphyseal dysplasia Panel

By Centre of Molecular Diseases (CMM) CHUV
This panel specifically test the NKX3-2 gene.
More info about this panel
Spondylo-megaepiphyseal-metaphyseal dysplasia (sequence analysis of NKX3-2) Panel

By CGC Genetics
This panel specifically test the NKX3-2 gene.
More info about this panel
Skeletal dysplasia (NGS panel for 31 genes) Panel

By CGC Genetics Skeletal dysplasia (NGS panel for 31 genes) that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 NSDHL TRPV4 P3H1 SBDS SLC35D1 COL10A1
More info about this panel
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection Panel

By PreventionGenetics PreventionGenetics Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection that also includes the following genes: RMRP ROR2 RUNX2 SALL1 BMP1 BMP2 BMPR1B SF3B4 SH3BP2 FBXW4
More info about this panel
Spondylo-Epi-Metaphyseal dysplasias Deletion / Duplication panel Panel

By Connective Tissue Gene Tests Spondylo-Epi-Metaphyseal dysplasias Deletion / Duplication panel that also includes the following genes: RMRP BGN RUNX2 SLC26A2 SMARCAL1 ACP5 CFAP410 CCN6 XYLT1 RAB33B
More info about this panel
Skeletal dysplasia core & extended Deletion / Duplication panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia core & extended Deletion / Duplication panel that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 NSDHL TRPV4 SBDS SLC35D1 COL10A1 COL11A1
More info about this panel
Skeletal dysplasia core & extended Comprehensive panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia core & extended Comprehensive panel that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 NSDHL TRPV4 SBDS SLC35D1 COL10A1 COL11A1
More info about this panel
Skeletal dysplasia core Comprehensive panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia core Comprehensive panel that also includes the following genes: SLC26A2 SOX9 TRIP11 COL1A2 FGFR3 ALPL INPPL1 NKX3-2
More info about this panel
Skeletal dysplasia core NGS panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia core NGS panel that also includes the following genes: SLC26A2 SOX9 TRIP11 COL1A2 FGFR3 ALPL INPPL1 NKX3-2
More info about this panel
Spondylo-Epi-Metaphyseal dysplasias Comprehensive panel Panel

By Connective Tissue Gene Tests Spondylo-Epi-Metaphyseal dysplasias Comprehensive panel that also includes the following genes: RMRP BGN RUNX2 SLC26A2 SMARCAL1 ACP5 CFAP410 CCN6 XYLT1 RAB33B
More info about this panel
Spondylo-Epi-Metaphyseal dysplasias NGS panel Panel

By Connective Tissue Gene Tests Spondylo-Epi-Metaphyseal dysplasias NGS panel that also includes the following genes: RMRP BGN RUNX2 SLC26A2 SMARCAL1 ACP5 CFAP410 CCN6 XYLT1 RAB33B
More info about this panel
Skeletal dysplasia core & extended NGS panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia core & extended NGS panel that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 NSDHL TRPV4 SBDS SLC35D1 COL10A1 COL11A1
More info about this panel
Skeletal dysplasia core Deletion / Duplication panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia core Deletion / Duplication panel that also includes the following genes: SLC26A2 SOX9 TRIP11 COL1A2 FGFR3 ALPL INPPL1 NKX3-2
More info about this panel
Skeletal dysplasia and skeletal ciliopathy Comprehensive panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia and skeletal ciliopathy Comprehensive panel that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 CFAP410 NSDHL IFT122 IFT81 IFT52 TRPV4
More info about this panel
Skeletal dysplasia and skeletal ciliopathy NGS panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia and skeletal ciliopathy NGS panel that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 CFAP410 NSDHL IFT122 IFT81 IFT52 TRPV4
More info about this panel
Skeletal dysplasia and skeletal ciliopathy Deletion / Duplication panel Panel

By Connective Tissue Gene Tests Skeletal dysplasia and skeletal ciliopathy Deletion / Duplication panel that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 CFAP410 NSDHL IFT122 IFT81 IFT52 TRPV4
More info about this panel
Metaphyseal dysplasia panel Panel

By Centogene AG - the Rare Disease Company Metaphyseal dysplasia panel that also includes the following genes: RMRP RUNX2 ANKH CDKN1C FLNA MMP13 MMP9 NKX3-2
More info about this panel
Spondylo-megaepiphyseal-metaphyseal dysplasia Panel

By Centogene AG - the Rare Disease Company
This panel specifically test the NKX3-2 gene.
More info about this panel
Spondylometaphyseal dysplasia and Spondylo-epi-(meta)-physeal dysplasia Panel Panel

By CeGaT GmbH Spondylometaphyseal dysplasia and Spondylo-epi-(meta)-physeal dysplasia Panel that also includes the following genes: RMRP SMARCAL1 ACP5 CCN6 XYLT1 RAB33B B3GALT6 TRPV4 CHST3 CANT1
More info about this panel
Skeletal dysplasias Panel

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Skeletal dysplasias that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 CCN6 NSDHL TRPV4 SBDS EVC2 SLC35D1
More info about this panel
Disproportionate Short Stature: Sequencing Panel Panel

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Disproportionate Short Stature: Sequencing Panel that also includes the following genes: ROR2 RUNX2 BMPR1B SHOX SLC26A2 SMARCAL1 SOX9 TBCE TBX6 TRIP11
More info about this panel
Skeletal Dysplasia: Sequencing Panel Panel

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
Disproportionate Short Stature: Deletion/Duplication Panel Panel

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Disproportionate Short Stature: Deletion/Duplication Panel that also includes the following genes: ROR2 RUNX2 BMPR1B SHOX SLC26A2 SMARCAL1 SOX9 TBCE TRIP11 TRPS1
More info about this panel
Skeletal Dysplasias NGS panel Panel

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
NKX3-2 Panel

By Fulgent Genetics Fulgent Genetics
This panel specifically test the NKX3-2 gene.
More info about this panel
Spondylometaphyseal / Spondyloepi-(meta)-physeal Dysplasia Panel Panel

By Blueprint Genetics Spondylometaphyseal / Spondyloepi-(meta)-physeal Dysplasia Panel that also includes the following genes: RMRP BGN SMARCAL1 ACP5 CCN6 RAB33B B3GALT6 TRPV4 CHST3 CANT1
More info about this panel
Comprehensive Skeletal Dysplasias and Disorders Panel Panel

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
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel Panel

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
SKELETAL DYSPLASIA NGS PANEL Panel

By Laboratorio de Genetica Clinica SL SKELETAL DYSPLASIA NGS PANEL that also includes the following genes: SLC26A2 SOX9 TRIP11 TRPV4 EVC2 SLC35D1 COL10A1 COL11A1 COL11A2 COL1A2
More info about this panel
Skeletal Dysplasias , Panel Massive Sequencing (NGS) 36 Genes Panel

By Reference Laboratory Genetics Skeletal Dysplasias , Panel Massive Sequencing (NGS) 36 Genes that also includes the following genes: RMRP SLC26A2 SOX9 TRIP11 CCN6 NSDHL TRPV4 SBDS EVC2 SLC35D1
More info about this panel
Tempus xO assay Panel

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
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