myosclerosis, autosomal recessive

Preferred Label : myosclerosis, autosomal recessive;

MeSH synonym : myopathy, myosclerotic; myosclerosis, congenital, of lowenthal;

Origin ID

C564968;

UMLS CUI

C1850671;

Currated CISMeF NLP mapping
- Myosclerosis, autosomal recessive [OMIM Phenotype]
- myosclerotic myopathy [Disease (Nov.)]
MeSH term(s) associated for indexing
- myopathies, structural, congenital [MeSH Descriptor]
Record concept(s)
- myosclerosis, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myosclerosis [MedDRA Preferred Term]
- Myosclerosis (disorder) [SNOMED CT concept]
- Myosclerosis, autosomal recessive [OMIM Phenotype]
- myosclerotic myopathy [Disease (Nov.)]