retinitis pigmentosa, X-Linked, and sinorespiratory infections, with or without deafness

Preferred Label : retinitis pigmentosa, X-Linked, and sinorespiratory infections, with or without deafness;

MeSH note : mutations in RPGR;

Origin ID

C567595;

UMLS CUI

C2749137;

Currated CISMeF NLP mapping
- Retinitis pigmentosa, X-linked, and sinorespiratory infections with or without deafness [OMIM Phenotype]
MeSH term(s) associated for indexing
- deafness [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- respiratory tract infections [MeSH Descriptor]
- retinitis pigmentosa [MeSH Descriptor]
Record concept(s)
- retinitis pigmentosa, X-Linked, and sinorespiratory infections, with or without deafness [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Retinitis pigmentosa, X-linked, and sinorespiratory infections with or without deafness [OMIM Phenotype]