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DOID:0110236 - cataract 39 multiple types
Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34.
Synonyms: CTRCT39, autosomal dominant cataract 39 multiple types,
Xenbase Genes :
MONDO:0014075 - cataract 39 multiple types |
Other Model Organisms: AGR, 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)