EDARADD gene related symptoms and diseases
All the information presented here about the EDARADD gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to EDARADD gene
| Symptoms // Phenotype | % Cases | 
|---|---|
| Hypohidrosis | Common - Between 50% and 80% cases | 
| Dry skin | Common - Between 50% and 80% cases | 
| Abnormality of dental morphology | Common - Between 50% and 80% cases | 
| Hypodontia | Common - Between 50% and 80% cases | 
| Hypotrichosis | Common - Between 50% and 80% cases | 
Other less frequent symptoms and clinical features
Patients with EDARADD gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Thick vermilion border
 Not very common - Between 30% and 50% cases
- Abnormality of the fingernails
 - Anhidrosis
 - Abnormal number of teeth
 - Abnormality of the forehead
 - Hypohidrotic ectodermal dysplasia
 - Anhidrotic ectodermal dysplasia
 - Absent nipple
 
And 40 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to EDARADD gene
Here you will find a list of rare diseases related to the EDARADD. 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
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT; ECTD11A
Alternate names
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT; ECTD11A Is also known as hed, ectodermal dysplasia, hypohidrotic, autosomal dominant
Description
Some ectodermal dysplasias are here classified as congenital disorders characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.Hypohidrotic, or anhidrotic, ectodermal dysplasia (HED/EDA) is characterized by a triad of signs comprising sparse hair (hypotrichosis), abnormal or missing teeth (anodontia or hypodontia), and inability to sweat (anhidrosis or hypohidrosis). Typical clinical manifestations also include dryness of the skin, eyes, airways, and mucous membranes presumably due to the defective development of several exocrine glands. Hypohidrotic ectodermal dysplasia can be associated with dysmorphic features (forehead bumps, rings under the eyes, everted nose, and prominent lips) and occasionally with absent nipples (summary by Cluzeau et al., 2011).For a discussion of genetic heterogeneity of hypohidrotic/anhidrotic ectodermal dysplasia, see {305100}.
Most common symptoms of ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT; ECTD11A
- Hyperhidrosis
 - Sparse hair
 - Hypotrichosis
 - Dry skin
 - Thick vermilion border
 
More info about ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT; ECTD11A
SOURCES: OMIM
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B
Alternate names
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B Is also known as eda, ectodermal dysplasia, hypohidrotic, hed, ectodermal dysplasia, anhidrotic
Description
Some ectodermal dysplasias are here classified as congenital disorders characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.Hypohidrotic, or anhidrotic, ectodermal dysplasia (HED/EDA) is characterized by a triad of signs comprising sparse hair (hypotrichosis), abnormal or missing teeth (anodontia or hypodontia), and inability to sweat (anhidrosis or hypohidrosis). Typical clinical manifestations also include dryness of the skin, eyes, airways, and mucous membranes presumably due to the defective development of several exocrine glands. Hypohidrotic ectodermal dysplasia can be associated with dysmorphic features (forehead bumps, rings under the eyes, everted nose, and prominent lips) and occasionally with absent nipples (summary by Cluzeau et al., 2011).For a discussion of genetic heterogeneity of hypohidrotic/anhidrotic ectodermal dysplasia, see {305100}.
Most common symptoms of ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B
- Depressed nasal bridge
 - Fever
 - Recurrent respiratory infections
 - Hyperhidrosis
 - Respiratory tract infection
 
More info about ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B
SOURCES: OMIM
AUTOSOMAL DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA
Alternate names
AUTOSOMAL DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA Is also known as autosomal dominant anhidrotic ectodermal dysplasia, ad-hed
Most common symptoms of AUTOSOMAL DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA
- Abnormality of the dentition
 - Prominent forehead
 - Hypotrichosis
 - Abnormality of skin pigmentation
 - Thick vermilion border
 
More info about AUTOSOMAL DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA
SOURCES: ORPHANET
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
Search interest in EDARADD
Potential gene panels for EDARADD gene
EDARADD Gene Sequencing Panel
 United States.
By GeneDx
This panel specifically test the EDARADD 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.
EDARADD. Complete sequencing Panel
 Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
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.
Anhidrotic ectodermal dysplasia (sequence analysis of EDARADD gene) Panel
 Portugal.
By CGC Genetics
This panel specifically test the EDARADD gene.
More info about this panel
 Portugal.
Ectodermal dysplasia (NGS panel for 8 genes) Panel
 Portugal.
By CGC Genetics Ectodermal dysplasia (NGS panel for 8 genes) that also includes the following genes: EDARADD KRT74 EDAR EDA GJB6 HOXC13 KRT85 MSX1
More info about this panel
 Portugal.
Ectodermal dysplasia (NGS panel for 8 genes) Panel
 Portugal.
By CGC Genetics Ectodermal dysplasia (NGS panel for 8 genes) that also includes the following genes: EDARADD KRT74 EDAR EDA GJB6 HOXC13 KRT85 MSX1
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 EDARADD Gene Sequencing with CNV Detection Panel
 United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the EDARADD 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.
Ectodermal dysplasia Comprehensive panel Panel
 United States.
By Connective Tissue Gene Tests Ectodermal dysplasia Comprehensive panel that also includes the following genes: EDARADD KDF1 KRT74 EDAR EDA GJB6 HOXC13 KRT85 MSX1
More info about this panel
 United States.
Ectodermal dysplasia Deletion / Duplication panel Panel
 United States.
By Connective Tissue Gene Tests Ectodermal dysplasia Deletion / Duplication panel that also includes the following genes: EDARADD KDF1 KRT74 EDAR EDA GJB6 HOXC13 KRT85 MSX1
More info about this panel
 United States.
Ectodermal dysplasia NGS panel Panel
 United States.
By Connective Tissue Gene Tests Ectodermal dysplasia NGS panel that also includes the following genes: EDARADD KDF1 KRT74 EDAR EDA GJB6 HOXC13 KRT85 MSX1
More info about this panel
 United States.
Ectodermal dysplasia, hypohidrotic AR Panel
 Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the EDARADD gene.
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 Hypohidrotic Ectodermal Dysplasia, Autosomal Panel
 United Kingdom.
By All Wales Genetics Laboratory Institute of Medical Genetics Test for Hypohidrotic Ectodermal Dysplasia, Autosomal that also includes the following genes: EDARADD EDAR
More info about this panel
 United Kingdom.
Ectodermal dysplasia, hypohidrotic Panel
 Austria.
By Praxis fuer Humangenetik Wien
This panel specifically test the EDARADD gene.
More info about this panel
 Austria.
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.
Ectodermal dysplasia, hypohidrotic Panel
 Slovakia.
By MedGene
This panel specifically test the EDARADD 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.
Hypohidrotic Ectodermal dysplasia: EDARADD gene sequence analysis Panel
 Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
This panel specifically test the EDARADD 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.
Hypohidrotic ectodermal dysplasia Panel
 Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Hypohidrotic ectodermal dysplasia that also includes the following genes: EDARADD EDAR EDA
More info about this panel
 Spain.
Hypohidrotic Ectodermal Dysplasia: Sequencing Panel Panel
 United States.
By EGL Genetic Diagnostics Eurofins Clinical Diagnostics Hypohidrotic Ectodermal Dysplasia: Sequencing Panel that also includes the following genes: EDARADD EDAR EDA
More info about this panel
 United States.
Ectodermal Dysplasia NGS Panel Panel
 United States.
By Fulgent Genetics Fulgent Genetics Ectodermal Dysplasia NGS Panel that also includes the following genes: EDARADD EDAR EDA
More info about this panel
 United States.
EDARADD Panel
 United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the EDARADD 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.
Ectodermal Dysplasia via the EDARADD Gene Panel
 Iran.
By Genomic Research Center Shahid Beheshti University of Medical Sciences
This panel specifically test the EDARADD gene.
More info about this panel
 Iran.
Hypohidrotic autosomal recessive ectodermal dysplasia Panel
 Spain.
By Bioarray
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
Autosomal hypohidrotic ectodermal dysplasia Panel
 Spain.
By Bioarray
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
Ectodermal Dysplasia via the EDARADD Gene Panel
 Iran.
By Center for Comprehensive Genetic Services Shahid Beheshti University of Medical Sciences
This panel specifically test the EDARADD gene.
More info about this panel
 Iran.
HYPOHIDROTIC/ANHIDROTIC ECTODERMAL DYSPLASIA Panel
 Spain.
By Laboratorio de Genetica Clinica SL HYPOHIDROTIC/ANHIDROTIC ECTODERMAL DYSPLASIA that also includes the following genes: EDARADD EDAR EDA
More info about this panel
 Spain.
Autosomal Recessive Hypohidrotic Ectodermal Dysplasia Type 11B , Sequencing EDARADD Gene Panel
 Spain.
By Reference Laboratory Genetics
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
Autosomal Dominant Hypohidrotic Ectodermal Dysplasia Type 11A , Sequencing EDARADD Gene Panel
 Spain.
By Reference Laboratory Genetics
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
Autosomal Dominant Hypohidrotic Ectodermal Dysplasia Type 11A , Deletions-Duplications (MLPA) EDARADD Gene Panel
 Spain.
By Reference Laboratory Genetics
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
Autosomal Recessive Hypohidrotic Ectodermal Dysplasia Type 11B , Deletions-Duplications (MLPA) EDARADD Gene Panel
 Spain.
By Reference Laboratory Genetics
This panel specifically test the EDARADD gene.
More info about this panel
 Spain.
Hypohidrotic Ectodermal Dysplasia , Massive Sequencing (NGS) EDA,EDAR and EDARADD Genes Panel
 Spain.
By Reference Laboratory Genetics Hypohidrotic Ectodermal Dysplasia , Massive Sequencing (NGS) EDA,EDAR and EDARADD Genes that also includes the following genes: EDARADD EDAR EDA
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.
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Panel
 Germany.
By Labor Dr. Wisplinghoff
This panel specifically test the EDARADD gene.
More info about this panel
 Germany.
Autosomal dominant hypohidrotic ectodermal dysplasia Panel
 Germany.
By Labor Dr. Wisplinghoff
This panel specifically test the EDARADD gene.
More info about this panel
 Germany.
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