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Summary Literature (0)
DOID:0110241 - cataract 41

Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.

Synonyms: congenital nuclear type cataract 41, CTRCT41

Xenbase Genes : wfs1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007287 - cataract 41

MIM:
MIM:116400 - CATARACT 41; CTRCT41

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)