About   Help   FAQ
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
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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory