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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 on chromosome 1p13.

Synonyms: ACHM4,

Xenbase Genes : gnat2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013465 - achromatopsia 4


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

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