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Echinobase
Summary Literature (0)
DOID:0110008 - achromatopsia 3

Disease Ontology Definition:An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.

Synonyms: ACHM1, ACHM3, Pingelapese blindness, RMCH1, rod monochromacy 1, rod monochromatism 1,

Echinobase Genes :


OMIM:
MIM:262300 - achromatopsia 3; achm3

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

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