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Summary Literature (3)
DOID:13911 - achromatopsia


Disease Ontology Definition:A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance.

Synonyms: ACHM, Monochromatism

Xenbase Genes : pde6c, cnga3, opn1lw, atf6, pde6h, cngb3, gnat2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018852 - achromatopsia


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

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