About   Help   FAQ
Disease Ontology Browser
retinitis pigmentosa 49 (DOID:0110377)
Alliance: disease page
Synonyms: RP49
Alt IDs: OMIM:613756, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12.

Disease References using Mouse Models (2)
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
11/12/2024
MGI 6.24 		The Jackson Laboratory