| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A variant of retinitis pigmentosa characterized by areas of choroidal degeneration with pigment migration and bony spicule formation in the macular area. In contrast to more typical forms of RP, this anomaly destroys central vision, leaving peripheral vision intact. (Human Phenotype Ontology, HP_0008035) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008035 |
| Similar Terms | |
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2 genes associated with the retinitis pigmentosa inversa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
