OBO ID: DOID:0110245
Term Name: cataract 38 Search Ontology:
Synonyms:
  • autosomal recessive congenital cataract 5
  • CATC5
  • CTRCT38
Definition: A cataract that has_material_basis_in homozygous mutation in the AGK gene on chromosome 7q34. https://www.ncbi.nlm.nih.gov/pubmed/22415731
References:
  • ICD10CM:Q12.0
  • MIM:614691
Ontology: Human Disease   ( DOID:0110245 )
Relationships
is a type of:
OTHER cataract 38 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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