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Summary Literature (0)
DOID:0110259 - cataract 43

Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the UNC45B gene on chromosome 17q12.

Synonyms: CTRCT43

Xenbase Genes : unc45b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014565 - cataract 43

MIM:
MIM:616279 - CATARACT 43; CTRCT43

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

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