Search Ontology:
Human Disease

cataract 33

Term ID
DOID:0110264
Synonyms
  • cortical cataract 33
  • CTRCT33
Definition
A cataract that has_material_basis_in homozygous mutation in the beaded filament structural protein-1 gene (BFSP1) on chromosome 20p12. https://www.ncbi.nlm.nih.gov/pubmed/17225135
References
Ontology
Human Disease   ( DOID:0110264 )
Relationships
is a type of
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Genes Involved
Zebrafish Models