inclusion body myopathy autosomal recessive

Preferred Label : inclusion body myopathy autosomal recessive;

MeSH synonym : inclusion body myopathy 2, autosomal recessive; inclusion body myopathy quadriceps sparing; inclusion body myopathy, Quadriceps-Sparing; inclusion body myopathy, autosomal recessive;

Details

Origin ID

C538329;

UMLS CUI

C1833373;

Automatic exact mappings (from CISMeF team)
- Inclusion body myopathy 2 (disorder) [SNOMED CT concept]
- Inclusion body myopathy 2, autosomal recessive [OMIM Phenotype]
- Nonaka myopathy [OMIM Phenotype]
DO Cross reference
- GNE myopathy [DO Concept]
MeSH term(s) associated for indexing
- myositis, inclusion body [MeSH Descriptor]
Record concept(s)
- Inclusion body myopathy autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Inclusion body myopathy 2, autosomal recessive [OMIM Phenotype]

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