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Disease Ontology Browser
retinitis pigmentosa 13 (DOID:0110403)
Alliance: disease page
Synonyms: RP13
Alt IDs: OMIM:600059, ICD10CM:H35.5, MESH:C564008
Definition: A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3.

Disease References using Mouse Models (1)
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)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory