About   Help   FAQ
Disease Ontology Browser
retinitis pigmentosa 7 (DOID:0110383)
Alliance: disease page
Synonyms: RP7
Alt IDs: OMIM:608133, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.

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 & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.17
The Jackson Laboratory