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Echinobase
Summary Literature (0)
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,

Echinobase Genes : opn1lw



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)