Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia   703544004

SNOMED CT code


SNOMED code703544004
nameInclusion body myopathy with early-onset Paget disease and frontotemporal dementia
statusactive
date introduced2014-07-31
fully specified name(s)Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)
synonyms
  • Lower motor neuron degeneration with Paget-like bone disease
  • Pagetoid amyotrophic lateral sclerosis
  • Muscular dystrophy limb-girdle with Paget disease of bone
  • Pagetoid neuroskeletal syndrome
  • Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
  • IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteSkeletal muscle structure   127954009
parents
  • Autosomal dominant hereditary disorder   11164009
  • Myopathy with cytoplasmic inclusions   240086009
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia   703544004

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
              Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia   703544004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia   703544004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia   703544004

ancestors
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