retinitis pigmentosa 41

Preferred Label : retinitis pigmentosa 41;

MeSH note : mutations in PROM1; aka RP41;

MeSH synonym : retinal degeneration, autosomal recessive, Prominin-Related;

Details

Origin ID

C567422;

UMLS CUI

C2677516;

Currated CISMeF NLP mapping
- Retinitis pigmentosa 41 [OMIM Phenotype]
- retinitis pigmentosa 41 [DO Concept]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- retinitis pigmentosa 41 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinitis pigmentosa 41 [OMIM Phenotype]
- retinitis pigmentosa 41 [DO Concept]

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