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Disease Ontology Browser
retinitis pigmentosa 10 (DOID:0110388)
Alliance: disease page
Synonyms: RP10
Alt IDs: OMIM:180105, ICD10CM:H35.5, MESH:C566715
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32.


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
07/02/2024
MGI 6.13
The Jackson Laboratory