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DOID:0110253 - cataract 14 multiple types
Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the gene encoding gap junction protein alpha-3 (GJA3) on chromosome 13q12.
Synonyms: CAE3, CTRCT14, zonular pulverulent cataract 3, CZP3
Echinobase Genes

MIM:601885 - cataract 14, multiple types; ctrct14 |
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)