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Disease Ontology Browser
achromatopsia 2 (DOID:0110007)
Alliance: disease page
Synonyms: ACHM2; RMCH2; rod monochromacy 2; rod monochromatism 2
Alt IDs: OMIM:216900
Definition: An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11.

Disease References using Mouse Models (4)

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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last database update
MGI 6.20
The Jackson Laboratory