| Term Name: | retinitis pigmentosa 80 |
|---|---|
| Synonyms: | RP80 |
| Definition: | A retinitis pigmentosa that has_material_basis_in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13. |
| Ontology: | Human Disease [DOID:0061111] ( DOID:0061111 ) |