ophthalmoplegic neuromuscular disorder with abnormal mitochondria

Preferred Label : ophthalmoplegic neuromuscular disorder with abnormal mitochondria;

Origin ID

C564925;

UMLS CUI

C1850302;

Currated CISMeF NLP mapping
- Ophthalmoplegic neuromuscular disorder with abnormal mitochondria [OMIM Phenotype]
MeSH term(s) associated for indexing
- mitochondrial diseases [MeSH Descriptor]
- muscular diseases [MeSH Descriptor]
- ophthalmoplegia [MeSH Descriptor]
Record concept(s)
- ophthalmoplegic neuromuscular disorder with abnormal mitochondria [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ophthalmoplegic neuromuscular disorder with abnormal mitochondria [OMIM Phenotype]