retinitis pigmentosa 39 Disease Ontology Browser

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Disease Ontology Browser

retinitis pigmentosa 39 (DOID:0110360)
Alliance: disease page
Synonyms: RP39
Alt IDs: OMIM:613809, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the USH2A gene on chromosome 1q41.

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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