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Disease Ontology Browser
hypohidrotic ectodermal dysplasia (DOID:14793)
Synonyms: anhidrotic ectodermal dysplasia 3; Christ-Siemens-Touraine Syndrome; Ectodermal Dysplasia 1, Anhydrotic; Hypohidrotic X-linked ectodermal dysplasia (disorder)
Alt IDs: OMIM:129490, OMIM:224900, OMIM:300291, OMIM:305100, DOID:0050446, DOID:0050447, MESH:D053358, NCI:C84562, UMLS_CUI:C0162359
Definition: A monogenic disease that is characterized by malformation of ectodermal (skin, hair, teeth and sweat glands) structures including hypotrichosis (sparseness of scalp and body hair), hypohidrosis (reduced ability to sweat), and hypodontia (congenital absence of teeth).

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/13/2017
MGI 6.10
The Jackson Laboratory