About   Help   FAQ
Disease Ontology Browser
achromatopsia 2 (DOID:0110007)
Alliance: disease page
Synonyms: ACHM2; RMCH2; rod monochromacy 2; rod monochromatism 2
Alt IDs: OMIM:216900, MESH:C536128
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.24
The Jackson Laboratory