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Echinobase
Summary Literature (0)
DOID:0110010 - achromatopsia 4

Disease Ontology Definition:An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the GNAT2 gene (139340) on chromosome 1p13.

Synonyms: ACHM4,

Echinobase Genes :


OMIM:
MIM:613856 - achromatopsia 4; achm4

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): achromatopsia (is_a)