OBO ID: DOID:11367
Term Name: congenital aphakia Search Ontology:
Synonyms:
  • APHAKIA, CONGENITAL PRIMARY
  • Congenital absence of lens
Definition:
References:
  • ICD10CM:Q12.3
  • ICD9CM:743.35
  • NCI:C35172
  • OMIM:610256
  • SNOMEDCT_US_2023_03_01:35387008
  • UMLS_CUI:C0152422
Ontology: Human Disease   ( DOID:11367 )
Relationships
is a type of:
OTHER congenital aphakia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FOXE3 Anterior segment dysgenesis 2, multiple subtypes 610256
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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