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Disease Ontology Browser
achromatopsia 4 (DOID:0110010)
Alliance: disease page
Synonyms: ACHM4
Alt IDs: OMIM:613856
Definition: An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the GNAT2 gene (139340) on chromosome 1p13.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory