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Summary Literature (0)
DOID:0110261 - cataract 35

Disease Ontology Definition:A cataract that has_material_basis_in variation in the region 19q13.

Synonyms: CATCN1, CTRCT35, autosomal recessive congenital nuclear cataract 1, cataract 35, congenital nuclear,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012260 - cataract 35


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

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