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Disease Ontology Browser
achromatopsia 3 (DOID:0110008)
Alliance: disease page
Synonyms: ACHM1; ACHM3; Pingelapese blindness; RMCH1; rod monochromacy 1; rod monochromatism 1
Alt IDs: OMIM:262300, MESH:C536129
Definition: An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2.

Disease References using Mouse Models (3)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory