nemaline myopathy 2

Preferred Label : nemaline myopathy 2;

MeSH synonym : nemaline myopathy caused by mutation in the nebulin gene;

Origin ID

C538349;

UMLS CUI

C1850569;

Currated CISMeF NLP mapping
- Nemaline Myopathy 2 [NCIt concept]
- Nemaline myopathy 2 [OMIM Phenotype]
- nemaline myopathy 2 [DO Concept]
MeSH term(s) associated for indexing
- myopathies, nemaline [MeSH Descriptor]
Record concept(s)
- Nemaline Myopathy 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Nemaline Myopathy 2 [NCIt concept]
- Nemaline myopathy 2 [OMIM Phenotype]
- nemaline myopathy 2 [DO Concept]