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Disease Ontology Browser
retinitis pigmentosa 41 (DOID:0110376)
Alliance: disease page
Synonyms: RP41
Alt IDs: OMIM:612095, ICD10CM:H35.5, MESH:C567422
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the PROM1 gene on chromosome 4p15.

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)
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last database update
02/13/2024
MGI 6.23
The Jackson Laboratory