brody myopathy

Preferred Label : brody myopathy;

MeSH synonym : autosomal recessive brody myopathy; brody disease;

Origin ID

C536607;

UMLS CUI

C1832918;

Currated CISMeF NLP mapping
- Brody disease [OMIM Phenotype]
- Brody myopathy [DO Concept]
- Brody myopathy [ORDO Disease]
- Brody myopathy (disorder) [SNOMED CT concept]
DO Cross reference
- Brody myopathy [DO Concept]
MeSH term(s) associated for indexing
- myotonia congenita [MeSH Descriptor]
ORDO relation(s)
- Brody myopathy [ORDO Disease]
Record concept(s)
- Brody myopathy [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Brody disease [OMIM Phenotype]
- Brody myopathy [ORDO Disease]
- Brody myopathy [DO Concept]
- Brody myopathy (disorder) [SNOMED CT concept]