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Ontology Browser

Term:
Ectodermal Dysplasia 3, Anhidrotic (DOID:9003272)
Annotations: Rat: (3) Mouse: (3) Human: (3) Chinchilla: (3) Bonobo: (3) Dog: (3) Squirrel: (3) Pig: (3)
Parent Terms Term With Siblings Child Terms
Anhidrotic Ectodermal Dysplasia 1 +   
Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant  
Ectodermal Dysplasia 15, Hypohidrotic/Hair Type  
Ectodermal Dysplasia 3, Anhidrotic  
An autosomal dominant form of ectodermal dysplasia which is due to mutations in the gene for the EDAR RECEPTOR.
Hypohidrotic Ectodermal Dysplasia with Hypothyroidism and Ciliary Dyskinesia 
Hypohidrotic Ectodermal Dysplasia, Autosomal Recessive +   
Hypohidrotic Ectodermal Dysplasia, with Hypothyroidism and Agenesis of the Corpus Callosum 
Hypohidrotic Ectodermal Dysplasia, with Immune Deficiency  

Synonyms
Exact Synonyms: AUTOSOMAL DOMINANT HYPOHIDROTIC ECTODERMAL DYSPLASIA ;   ECTD10A ;   ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT ;   ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT ;   HED ;   autosomal dominant ectodermal dysplasia-10A
Primary IDs: MESH:D053359
Alternate IDs: OMIM:129490 ;   RDO:0007616
Definition Sources: MESH:D053359

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.