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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,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0009875 - achromatopsia 3 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee