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Summary Literature (0)
DOID:0110245 - cataract 38

Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the AGK gene on chromosome 7q34.

Synonyms: autosomal recessive congenital cataract 5, CATC5, CTRCT38

Xenbase Genes : agk

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013859 - cataract 38

MIM:
MIM:614691 - CATARACT 38; CTRCT38

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)