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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:0018852 - achromatopsia |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
color blindness (is_a)