Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
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: CATC5, CTRCT38, autosomal recessive congenital cataract 5

Echinobase Genes : agk


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)