About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory