Search Ontology:
Human Disease

cataract 39 multiple types

Term ID
DOID:0110236
Synonyms
  • autosomal dominant cataract 39 multiple types
  • CTRCT39
Definition
A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34. https://www.ncbi.nlm.nih.gov/pubmed/23288985
References
Ontology
Human Disease   ( DOID:0110236 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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