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Disease Ontology Browser
retinitis pigmentosa 33 (DOID:0110366)
Alliance: disease page
Synonyms: RP33
Alt IDs: OMIM:610359, ICD10CM:H35.5, MESH:C563676
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the SNRNP200 gene on chromosome 2q11.


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
04/09/2024
MGI 6.23
The Jackson Laboratory