retinitis pigmentosa 14

Preferred Label : retinitis pigmentosa 14;

MeSH note : mutation in TULP1;

MeSH synonym : retinitis pigmentosa, juvenile, TULP1-Related;

Origin ID

C563992;

UMLS CUI

C1838603;

Automatic exact mappings (from CISMeF team)
- Leber congenital amaurosis 15 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Retinitis pigmentosa 14 [OMIM Phenotype]
- retinitis pigmentosa 14 [DO Concept]
- retinitis pigmentosa 14 [Disease (Nov.)]
MeSH term(s) associated for indexing
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- retinitis pigmentosa 14 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinitis pigmentosa 14 [OMIM Phenotype]
- retinitis pigmentosa 14 [DO Concept]
- retinitis pigmentosa 14 [Disease (Nov.)]