Search Ontology:
Human Disease
ectodermal dysplasia
- Term ID
- DOID:2121
- Synonyms
-
- Congenital ectodermal defect
- Congenital ectodermal dysplasia
- Definition
- A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings. (3)
- References
-
- GARD:6317
- ICD9CM:757.31
- MESH:D004476
- MIM:PS305100
- NCI:C84683
- ORDO:79373
- SNOMEDCT_US_2023_03_01:8654005
- UMLS_CUI:C0013575
- Ontology
- Human Disease ( DOID:2121 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models