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DOID:0110256 - cataract 21 multiple types
Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the MAF gene on chromosome 16q23.
Synonyms: CCA4, CTRCT21, cataract 21 multiple types with or without microcornea, congenital cataract Cerulean type 4,
Xenbase Genes : maf
MONDO:0012437 - cataract 21 multiple types |
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)