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Summary Literature (1)
DOID:0110007 - achromatopsia 2

Disease Ontology Definition:An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.

Synonyms: ACHM2, RMCH2, rod monochromacy 2, rod monochromatism 2,

Xenbase Genes : cnga3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009003 - achromatopsia 2


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

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