retinitis pigmentosa 7, digenic

Preferred Label : retinitis pigmentosa 7, digenic;

MeSH note : digenic mutations in PRPH2 (RDS) and ROM1;

Origin ID

C567263;

UMLS CUI

C2675552;

Automatic exact mappings (from CISMeF team)
- Retinitis pigmentosa 7 [OMIM Phenotype]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- retinitis pigmentosa 7, digenic [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]