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Disease Ontology Browser
retinitis pigmentosa 13 (DOID:0110403)
Alliance: disease page
Synonyms: RP13
Alt IDs: OMIM:600059, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutations in the PRPF8 gene on chromosome 17p13.3.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory