WNT10A gene related symptoms and diseases

All the information presented here about the WNT10A gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to WNT10A gene

Symptoms // Phenotype % Cases
Abnormality of dental morphology Common - Between 50% and 80% cases
Dry skin Common - Between 50% and 80% cases
Hypodontia Common - Between 50% and 80% cases
Alopecia Uncommon - Between 30% and 50% cases
Nail dystrophy Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with WNT10A gene alterations may also develop some of the following symptoms and phenotypes:
  • Not very common - Between 30% and 50% cases

  • Conical incisor
  • Plantar hyperkeratosis
  • Anodontia
  • Agenesis of permanent teeth
  • Reduced number of teeth
  • Palmoplantar hyperkeratosis
  • Oligodontia
  • Ectodermal dysplasia

And 61 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to WNT10A gene

Here you will find a list of rare diseases related to the WNT10A. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


AUTOSOMAL RECESSIVE HYPOHIDROTIC ECTODERMAL DYSPLASIA

Alternate names

AUTOSOMAL RECESSIVE HYPOHIDROTIC ECTODERMAL DYSPLASIA Is also known as ar-hed, autosomal recessive anhidrotic ectodermal dysplasia

Most common symptoms of AUTOSOMAL RECESSIVE HYPOHIDROTIC ECTODERMAL DYSPLASIA

  • Alopecia
  • Dry skin
  • Fine hair
  • Hypohidrosis
  • Abnormality of the hair


More info about AUTOSOMAL RECESSIVE HYPOHIDROTIC ECTODERMAL DYSPLASIA

SOURCES: ORPHANET

ODONTO-ONYCHO-DERMAL DYSPLASIA

Alternate names

ODONTO-ONYCHO-DERMAL DYSPLASIA Is also known as oodd

Description

Odonto-onycho-dermal dysplasia is a form of ectodermal dysplasia characterised by hyperkeratosis and hyperhidrosis of the palms and soles, atrophic malar patches, hypodontia, conical teeth, onychodysplasia, and dry and sparse hair.

Most common symptoms of ODONTO-ONYCHO-DERMAL DYSPLASIA

  • Intellectual disability
  • Hyperhidrosis
  • Photophobia
  • Erythema
  • Sparse hair


More info about ODONTO-ONYCHO-DERMAL DYSPLASIA

SOURCES: ORPHANET MESH OMIM

TOOTH AGENESIS, SELECTIVE, 4; STHAG4

Alternate names

TOOTH AGENESIS, SELECTIVE, 4; STHAG4 Is also known as tooth agenesis, selective, 4, with or without ectodermal dysplasia, lateral incisors, absence of, succedaneous teeth, agenesis of, lateral incisors, pegged or missing

Most common symptoms of TOOTH AGENESIS, SELECTIVE, 4; STHAG4

  • Sparse hair
  • Dry skin
  • Hypodontia
  • Reduced number of teeth
  • Sparse eyebrow


More info about TOOTH AGENESIS, SELECTIVE, 4; STHAG4

SOURCES: MESH OMIM

SCHÖPF-SCHULZ-PASSARGE SYNDROME

Alternate names

SCHÖPF-SCHULZ-PASSARGE SYNDROME Is also known as palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome, keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis, eccrine tumors with ectodermal dysplasia, ssps, palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypot

Description

Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.

Most common symptoms of SCHÖPF-SCHULZ-PASSARGE SYNDROME

  • Neoplasm
  • Alopecia
  • Hyperhidrosis
  • Hyperkeratosis
  • Carcinoma


More info about SCHÖPF-SCHULZ-PASSARGE SYNDROME

SOURCES: ORPHANET MESH OMIM

OLIGODONTIA

Alternate names

OLIGODONTIA Is also known as selective tooth agenesis

Description

Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth.

Most common symptoms of OLIGODONTIA

  • Micrognathia
  • Hypoplasia of the maxilla
  • Microdontia
  • Abnormality of the face
  • Oligodontia


More info about OLIGODONTIA

SOURCES: ORPHANET


Potential gene panels for WNT10A gene

WNT10A Panel

Germany.

By Institute for Human Genetics University Clinic Freiburg

This panel specifically test the WNT10A gene.

More info about this panel
Germany.

WNT10A Gene Sequencing Panel

United States.

By GeneDx

This panel specifically test the WNT10A gene.

More info about this panel
United States.

TP63,EDA,EDAR,EDARADD,WNT10A, NextGeneDx.Complete sequencing by NGS Panel

Spain.

By Instituto de Medicina Genomica Instituto de Medicina Genomica TP63,EDA,EDAR,EDARADD,WNT10A, NextGeneDx.Complete sequencing by NGS that also includes the following genes: WNT10A EDARADD TP63 EDAR EDA

More info about this panel
Spain.

WNT10A. Complete sequencing Panel

Spain.

By Instituto de Medicina Genomica Instituto de Medicina Genomica

This panel specifically test the WNT10A gene.

More info about this panel
Spain.

Odontoonychodermal dysplasia (sequence analysis of WNT10A gene) Panel

Portugal.

By CGC Genetics

This panel specifically test the WNT10A gene.

More info about this panel
Portugal.

Ectodermal dysplasia 1, hypohidrotic, X-linked (deletion/duplication analysis of genes EDA, EDAR, EDARADD and WNT10A) Panel

Portugal.

By CGC Genetics Ectodermal dysplasia 1, hypohidrotic, X-linked (deletion/duplication analysis of genes EDA, EDAR, EDARADD and WNT10A) that also includes the following genes: WNT10A EDARADD EDAR EDA

More info about this panel
Portugal.

Ectodermal Dysplasia Sequencing Panel with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics Ectodermal Dysplasia Sequencing Panel with CNV Detection that also includes the following genes: WNT10A EDARADD EDAR EDA KRT85 NECTIN1

More info about this panel
United States.

Ectodermal Dysplasia via WNT10A Gene Sequencing with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Tooth Agenesis Sequencing Panel with CNV Detection Panel

United States.

By PreventionGenetics PreventionGenetics Tooth Agenesis Sequencing Panel with CNV Detection that also includes the following genes: WNT10A EDARADD EDAR EDA LTBP3 MSX1 PAX9 AXIN2

More info about this panel
United States.

Oligodontia - Selective tooth agenesis Comprehensive panel Panel

United States.

By Connective Tissue Gene Tests Oligodontia - Selective tooth agenesis Comprehensive panel that also includes the following genes: WNT10B WNT10A EDA LRP6 LTBP3 MSX1 PAX9 AXIN2 PTH1R

More info about this panel
United States.

Oligodontia - Selective tooth agenesis NGS panel Panel

United States.

By Connective Tissue Gene Tests Oligodontia - Selective tooth agenesis NGS panel that also includes the following genes: WNT10B WNT10A EDA LRP6 LTBP3 MSX1 PAX9 AXIN2 PTH1R

More info about this panel
United States.

Oligodontia - Selective tooth agenesis Deletion / Duplication panel Panel

United States.

By Connective Tissue Gene Tests Oligodontia - Selective tooth agenesis Deletion / Duplication panel that also includes the following genes: WNT10B WNT10A EDA LRP6 LTBP3 MSX1 PAX9 AXIN2 PTH1R

More info about this panel
United States.

Odontoonychodermal dysplasia Sequencing test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Schopf-Schulz-Passarge syndrome Sequencing test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Schopf-Schulz-Passarge syndrome Comprehensive test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Schopf-Schulz-Passarge syndrome Deletion / Duplication test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Odontoonychodermal dysplasia Comprehensive test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Tooth agenesis, selective, 4 Deletion / Duplication test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Tooth agenesis, selective, 4 Sequencing test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Odontoonychodermal dysplasia Deletion / Duplication test Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Tooth agenesis, selective, 4 Comprehensivetest Panel

United States.

By Connective Tissue Gene Tests

This panel specifically test the WNT10A gene.

More info about this panel
United States.

WNT10A Panel

Netherlands.

By Genome Diagnostics Laboratory University Medical Center Utrecht

This panel specifically test the WNT10A gene.

More info about this panel
Netherlands.

Odontoonychodermal dysplasia Panel

Germany.

By Centogene AG - the Rare Disease Company

This panel specifically test the WNT10A gene.

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.

Ichthyoses and related disorders of cornification Panel Panel

Germany.

By CeGaT GmbH Ichthyoses and related disorders of cornification Panel that also includes the following genes: SLC27A4 SNAP29 ST14 STS TAT TGM1 TGM5 VPS33B ATP2C1 NSDHL

More info about this panel
Germany.

Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel Panel

Germany.

By CeGaT GmbH Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel that also includes the following genes: BCS1L SNRPE SOX18 ST14 TRPS1 IFT122 WNT10A EDARADD SHOC2 LPAR6

More info about this panel
Germany.

Test for Odontoonychodermal Dysplasia Panel

United Kingdom.

By All Wales Genetics Laboratory Institute of Medical Genetics

This panel specifically test the WNT10A gene.

More info about this panel
United Kingdom.

Odontoonychodermal dysplasia Panel

Austria.

By Praxis fuer Humangenetik Wien

This panel specifically test the WNT10A gene.

More info about this panel
Austria.

Schopf-Schulz-Passarge syndrome Panel

Austria.

By Praxis fuer Humangenetik Wien

This panel specifically test the WNT10A gene.

More info about this panel
Austria.

Tooth agenesis, selective, 4 Panel

Austria.

By Praxis fuer Humangenetik Wien

This panel specifically test the WNT10A gene.

More info about this panel
Austria.

qCarrier Plus Panel

Spain.

By Quantitative Genomic Medicine Laboratories, SL qCarrier Plus that also includes the following genes: RMRP RP2 RPE65 RPGR RPS6KA3 RS1 SACS SGCA SGCB SGSH

More info about this panel
Spain.

qGenEx Craniofacial Anomalies Panel

Spain.

By Quantitative Genomic Medicine Laboratories, SL qGenEx Craniofacial Anomalies that also includes the following genes: RUNX2 SALL1 TSHZ1 BMP4 SEMA3E SF3B4 SH3BP2 SHH SIX1 SIX3

More info about this panel
Spain.

Odontoonychodermal dysplasia Panel

Slovakia.

By MedGene

This panel specifically test the WNT10A gene.

More info about this panel
Slovakia.

Tooth agenesis, selective, 4 Panel

Slovakia.

By MedGene

This panel specifically test the WNT10A gene.

More info about this panel
Slovakia.

Schopf-Schulz-Passarge syndrome Panel

Slovakia.

By MedGene

This panel specifically test the WNT10A gene.

More info about this panel
Slovakia.

Invitae Ectodermal Dysplasia with or without Tooth Agenesis Panel Panel

United States.

By Invitae Invitae Ectodermal Dysplasia with or without Tooth Agenesis Panel that also includes the following genes: WNT10A EDARADD EDAR EDA LTBP3 MSX1 NFKBIA PAX9

More info about this panel
United States.

Schopf-Schulz-Passarge syndrome: WNT10A gene sequence analysis Panel

Spain.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases

This panel specifically test the WNT10A gene.

More info about this panel
Spain.

Ectodermal dysplasia Panel

Spain.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Ectodermal dysplasia that also includes the following genes: TRAF6 WNT10A EDARADD TP63 CDH3 EDA2R EDAR EDA GJB6 IKBKG

More info about this panel
Spain.

WNT10A Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the WNT10A gene.

More info about this panel
United States.

Ectodermal Dysplasia Panel Panel

Finland.

By Blueprint Genetics Ectodermal Dysplasia Panel that also includes the following genes: RMRP BCS1L IFT122 WNT10A EDARADD TP63 MPLKIP CDH3 PORCN EVC2

More info about this panel
Finland.

Palmoplantar Keratoderma Panel Panel

Finland.

By Blueprint Genetics Palmoplantar Keratoderma Panel that also includes the following genes: WNT10A SERPINB7 MBTPS2 TRPV3 SLURP1 KRT6C CTSC AAGAB DSG1 DSP

More info about this panel
Finland.

ODONTO ONYCHO DERMAL DYSPLASIA Panel

Spain.

By Laboratorio de Genetica Clinica SL

This panel specifically test the WNT10A gene.

More info about this panel
Spain.

Odontoonychodermal Dysplasia , Sequencing WNT10A Panel

Spain.

By Reference Laboratory Genetics

This panel specifically test the WNT10A gene.

More info about this panel
Spain.

Schopf-Schulz-Passarge Syndrome , Sequencing WNT10A Gene Panel

Spain.

By Reference Laboratory Genetics

This panel specifically test the WNT10A gene.

More info about this panel
Spain.

Ectodermal Dysplasia , Panel Massive Sequencing (NGS) 9 Genes Panel

Spain.

By Reference Laboratory Genetics Ectodermal Dysplasia , Panel Massive Sequencing (NGS) 9 Genes that also includes the following genes: WNT10A EDARADD TP63 CDH3 EDAR EDA GJB6 IKBKG NFKBIA

More info about this panel
Spain.

Dentinogenesis Imperfecta, Panel Massive Sequencing (NGS) 4 Genes Panel

Spain.

By Reference Laboratory Genetics Dentinogenesis Imperfecta, Panel Massive Sequencing (NGS) 4 Genes that also includes the following genes: WNT10A DSPP MSX1 PTH1R

More info about this panel
Spain.

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.

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