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Disease Ontology Browser
ectodermal dysplasia 1 (DOID:0111664)
Alliance: disease page
Synonyms: Christ-Siemens-Touraine syndrome; CST syndrome; ectodermal dysplasia 1, anhidrotic; ectodermal dysplasia 1, hypohidrotic, X-linked; ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked; ED1; HED1; hypohidrotic ectodermal dysplasia, X-Linked; X-linked anhidrotic ectodermal dysplasia; XHED; XLHED
Alt IDs: OMIM:305100, MESH:D053358, NCI:C84562, ORDO:181, UMLS_CUI:C0162359
Definition: A hypohidrotic ectodermal dysplasia that has_material_basis_in X-linked recessive mutation in EDA on chromosome Xq13.1.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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03/25/2025
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