retinitis pigmentosa 18

Preferred Label : retinitis pigmentosa 18;

MeSH note : mutation in PRPF3;

Origin ID

C563320;

UMLS CUI

C1832378;

Currated CISMeF NLP mapping
- Retinitis pigmentosa 18 [OMIM Phenotype]
- retinitis pigmentosa 18 [DO Concept]
- retinitis pigmentosa 18 [Disease (Nov.)]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- retinitis pigmentosa 18 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinitis pigmentosa 18 [OMIM Phenotype]
- retinitis pigmentosa 18 [DO Concept]
- retinitis pigmentosa 18 [Disease (Nov.)]