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Disease Ontology Browser
retinitis pigmentosa 50 (DOID:0110396)
Alliance: disease page
Synonyms: RP50
Alt IDs: OMIM:613194, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the BEST1 gene on chromosome 11q13.


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
03/19/2024
MGI 6.23
The Jackson Laboratory