Search Ontology:
Human Disease

cataract 38

Term ID
DOID:0110245
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
Ontology
Human Disease   ( DOID:0110245 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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