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DOID:0110241 - cataract 41
Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.
Synonyms: CTRCT41, congenital nuclear type cataract 41,
Xenbase Genes : wfs1
MONDO:0007287 - cataract 41 |
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)