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Summary Literature (0)
DOID:0110258 - cataract 10 multiple types


Disease Ontology Definition:A cataract that has_material_basis_in heterozygous mutation in the CRYBA1 gene on chromosome 17q11.

Synonyms: CCZS, congenital zonular cataract with sutural opacities, CTRCT10

Xenbase Genes : cryba1, cryba1.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010948 - cataract 10 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)