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Summary Literature (0)
DOID:0110269 - cataract 3 multiple types

Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the beta-B2-crystallin gene (CRYBB2) on chromosome 22q11.

Synonyms: CCA2, CTRCT3, cataract 3 multiple types with or without microcornea, congenital Cerulean type cataract 2,

Xenbase Genes : crybb2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011104 - cataract 3 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)