Adult-onset distal myopathy due to valosin containing protein mutation   770792007

SNOMED CT code


SNOMED code770792007
nameAdult-onset distal myopathy due to valosin containing protein mutation
statusactive
date introduced2019-01-31
fully specified name(s)Adult-onset distal myopathy due to valosin containing protein mutation (disorder)
synonyms
  • Adult-onset distal myopathy due to VCP (valosin containing protein) mutation
  • Adult-onset distal myopathy due to VCP mutation
  • Adult-onset distal myopathy due to valosin containing protein mutation
attributes - group2
Associated morphologyDystrophy   4720007
Pathological processPathological developmental process   308490002
Finding siteSkeletal muscle structure   127954009
attributes - group3
Clinical courseProgressive   255314001
attributes - group1
OccurrenceAdulthood   41847000
Finding siteSkeletal muscle structure   127954009
Associated morphologyDystrophy   4720007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Distal muscular dystrophy   58795000
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
              Adult-onset distal myopathy due to valosin containing protein mutation   770792007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Distal muscular dystrophy   58795000
              Adult-onset distal myopathy due to valosin containing protein mutation   770792007

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