retinitis pigmentosa 78 Disease Ontology Browser

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Disease Ontology Browser

retinitis pigmentosa 78 (DOID:0061113)
Alliance: disease page
Synonyms: RP78
Alt IDs: OMIM:617433
Definition: A retinitis pigmentosa characterized by central visual disturbance, visual field defects, and nyctalopia that has_material_basis_in homozygous or compound heterozygous mutation in the ARHGEF18 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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