retinitis pigmentosa 102 Disease Ontology Browser

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retinitis pigmentosa 102 (DOID:0051093)
Alliance: disease page
Alt IDs: OMIM:621560
Definition: A retinitis pigmentosa that is charaterized by onset of night blindness and loss of peripheral vision in adolescence, and eventual reduction in visual acuity with progression of disease and that has_material_basis_in heterozygous mutation in the RNU4-2 gene on chromosome 12q24.

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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