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loading...| Preferred Name |
Retinitis Pigmentosa |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85045 |
| code |
C85045 |
| DEFINITION |
A rare inherited retinal dystrophy disorder characterized by spots of black bone-spicule pigmentation of the retinal pigment epithelium. It is manifested with decreased vision in low light or in the night, followed by decreased peripheral vision, and, eventual decreased central vision. It may lead to blindness. |
| label |
Retinitis Pigmentosa |
| Preferred_Name |
Retinitis Pigmentosa |
| prefixIRI |
C85045 |
| prefLabel |
Retinitis Pigmentosa |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0035334 |
| subClassOf |
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