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 )
Relationships
is a type of
has subtype
Other Pages
Genes Involved
Zebrafish Models