muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus

Preferred Label : muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0563074;

UMLS CUI

C0342281;

Currated CISMeF NLP mapping
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus [OMIM Phenotype]
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (disorder) [SNOMED CT concept]
- Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome [ORDO Disease]
Related record
- muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus [OMIM Phenotype]
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (disorder) [SNOMED CT concept]