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. (2)
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 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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