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Disease Ontology Browser
ectodermal dysplasia (DOID:2121)
Alliance: disease page
Synonyms: Congenital ectodermal defect; Congenital ectodermal dysplasia
Alt IDs: ICD9CM:757.31, MESH:D004476, NCI:C84683, OMIM:PS305100, ORDO:79373, UMLS_CUI:C0013575
Definition: A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.

Disease References using Mouse Models (10)
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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory