mitochondrial myopathy with a defect in mitochondrial protein transport

Preferred Label : mitochondrial myopathy with a defect in mitochondrial protein transport;

Origin ID

C565376;

UMLS CUI

C1855034;

Currated CISMeF NLP mapping
- Mitochondrial myopathy with a defect in mitochondrial-protein transport [OMIM Phenotype]
MeSH term(s) associated for indexing
- mitochondrial myopathies [MeSH Descriptor]
Record concept(s)
- mitochondrial myopathy with a defect in mitochondrial protein transport [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mitochondrial myopathy with a defect in mitochondrial-protein transport [OMIM Phenotype]