retinitis pigmentosa 97 Disease Ontology Browser

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Disease Ontology Browser

retinitis pigmentosa 97 (DOID:0061110)
Alliance: disease page
Synonyms: RP97
Alt IDs: OMIM:620422
Definition: A retinitis pigmentosa characterized by onset of night blindness and visual field defects in the first decade of life, with later onset of reduced visual acuity that has_material_basis_in heterozygous mutation in the VWA8 gene on chromosome 13q14.

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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