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Disease Ontology Browser
retinitis pigmentosa 26 (DOID:0110368)
Alliance: disease page
Synonyms: RP26
Alt IDs: OMIM:608380, ICD10CM:H35.5
Definition: A retinitis pigmentosa that has_material_basis_in mutation in the CERKL gene on chromosome 2q31.


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
02/11/2020
MGI 6.14
The Jackson Laboratory