retinitis pigmentosa 42

Preferred Label : retinitis pigmentosa 42;

MeSH note : aka RP42; associated with mtuation in KLHL7;

Origin ID

C567854;

UMLS CUI

C2751986;

Automatic exact mappings (from CISMeF team)
- kelch like family member 7 [ORDO Gene]
- kelch like family member 7 [HGNC gene]
Currated CISMeF NLP mapping
- Retinitis pigmentosa 42 [OMIM Phenotype]
- retinitis pigmentosa 42 [DO Concept]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- retinitis pigmentosa 42 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinitis pigmentosa 42 [OMIM Phenotype]
- retinitis pigmentosa 42 [DO Concept]