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Disease Ontology Browser
retinitis pigmentosa 106 (DOID:0051097)
Alliance: disease page
Alt IDs: OMIM:621564
Definition: A retinitis pigmentosa that is charaterized by onset of night blindness and/or loss of peripheral vision in adolescence and that has_material_basis_in heterozygous mutation in the RNU6-9 gene on chromosome 19p13.


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
07/14/2026
MGI 6.24
The Jackson Laboratory