Search Ontology:
Human Disease
ectodermal dysplasia
- Term ID
- DOID:2121
- Synonyms
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- 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. (2)
- References
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- GARD:6317
- ICD9CM:757.31
- MESH:D004476
- Ontology
- Human Disease ( DOID:2121 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models