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Disease Ontology Browser
retinitis pigmentosa 37 (DOID:0110399)
Alliance: disease page
Synonyms: RP37
Alt IDs: OMIM:611131, ICD10CM:H35.5, MESH:C567005
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the NR2E3 gene on chromosome 15q23.


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
01/24/2023
MGI 6.22
The Jackson Laboratory