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Disease Ontology Browser
retinitis pigmentosa 107 (DOID:0051098)
Alliance: disease page
Alt IDs: OMIM:621587
Definition: A retinitis pigmentosa that is charaterized by onset of RP ranging from the second decade to the sixth decade of life, with affected individuals experiencing night blindness, constriction of peripheral vision, and reduced visual acuity and that has_material_basis_in homozygous or compound heterozygous mutation in the CFAP20 gene on chromosome 16q21.

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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Send questions and comments to User Support. 		last database update
07/14/2026
MGI 6.24 		The Jackson Laboratory