Search Ontology:
Human Disease

congenital aphakia

Term ID
DOID:11367
Synonyms
  • APHAKIA, CONGENITAL PRIMARY
  • Congenital absence of lens
Definition
References
  • ICD10CM:Q12.3
  • ICD9CM:743.35
  • MIM:610256
  • NCI:C35172
  • SNOMEDCT_US_2023_03_01:35387008
  • UMLS_CUI:C0152422
Ontology
Human Disease   ( DOID:11367 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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