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Disease Ontology Browser
retinitis pigmentosa 12 (DOID:0110358)
Alliance: disease page
Synonyms: RP12
Alt IDs: OMIM:600105, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the CRB1 gene on chromosome 1q31.3.

Disease References using Mouse Models (2)

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
MGI 6.20
The Jackson Laboratory