Myopathy with cytoplasmic inclusions   240086009

SNOMED CT code


SNOMED code240086009
nameMyopathy with cytoplasmic inclusions
statusactive
date introduced2002-01-31
fully specified name(s)Myopathy with cytoplasmic inclusions (disorder)
synonymsMyopathy with cytoplasmic inclusions
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteSkeletal muscle structure   127954009
OccurrenceCongenital   255399007
parentsCongenital anomaly of skeletal muscle   89886004
children
  • Desmin related myopathy with Mallory body-like inclusions   715646003
  • Desmin-related myofibrillar myopathy   770627003
  • Hereditary inclusion body myopathy type 4   770786001
  • Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome   724349009
  • Inclusion body myopathy 2   702382000
  • Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia   703544004
  • X-linked myopathy with excessive autophagy   719815005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Muscle finding   106030000
      Disorder of muscle   129565002
        Disorder of skeletal muscle   75047002
          Congenital anomaly of skeletal muscle   89886004
            Myopathy with cytoplasmic inclusions   240086009

ancestors
sorted most to least specific
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