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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: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):
cataract (is_a)