Search Ontology:
Human Disease

cataract 12 multiple types

Term ID
DOID:0110239
Synonyms
  • CTRCT12
Definition
A cataract that has_material_basis_in heterozygous mutation in the gene encoding beaded filament structural protein-2 (BFSP2) on chromosome 3q22. https://www.ncbi.nlm.nih.gov/pubmed/10729115
References
Ontology
Human Disease   ( DOID:0110239 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models