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Disease Ontology Browser
achromatopsia 2 (DOID:0110007)
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 (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/18/2017
MGI 6.08
The Jackson Laboratory