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Summary Literature (0)
DOID:0110264 - cataract 33

Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the beaded filament structural protein-1 gene (BFSP1) on chromosome 20p12.

Synonyms: CTRCT33, cortical cataract 33

Xenbase Genes : bfsp1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012665 - cataract 33

MIM:
MIM:611391 - CATARACT 33, MULTIPLE TYPES; CTRCT33

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), cataract (is_a)