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Summary Literature (0)
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, congenital cataract Cerulean type 4, cataract 21 multiple types with or without microcornea, CTRCT21

Xenbase Genes : maf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012437 - epithelial-mesenchymal boundary

MIM:
MIM:610202 - CATARACT 21, MULTIPLE TYPES; CTRCT21

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal dominant disease (is_a), cataract (is_a)