Search Ontology: 
        
        Human Disease
            retinitis pigmentosa 7
- Term ID
- DOID:0110383
- Synonyms
- 
    
        
        - RP7
 
- Definition
- A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/1749427
- References
- 
    
        
        
    
    - ICD10CM:H35.5
- MESH:C564284
- MIM:608133
 
- Ontology
- Human Disease ( DOID:0110383 )
                
                    
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