Distal muscular dystrophy   58795000

SNOMED CT code


SNOMED code58795000
nameDistal muscular dystrophy
statusactive
date introduced2002-01-31
fully specified name(s)Distal muscular dystrophy (disorder)
synonyms
  • Distal myopathy
  • Distal muscular dystrophy
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDystrophy   4720007
Finding siteSkeletal muscle structure   127954009
attributes - group2
Clinical courseProgressive   255314001
parents
  • Autosomal hereditary disorder   1899006
  • Hereditary progressive muscular dystrophy   193225000
  • Muscular dystrophy not predominantly limb girdle in distribution   240070002
children
  • Adenylosuccinate synthetase-like 1-related distal myopathy   1172694007
  • Adult-onset distal myopathy due to valosin containing protein mutation   770792007
  • Benign congenital muscular dystrophy with finger flexion contractures   240078009
  • Distal anoctaminopathy   783166000
  • Distal muscular dystrophy with juvenile onset   193230001
  • Distal muscular dystrophy, Miyoshi type   111506000
  • Distal myopathy 2   702383005
  • Distal myopathy Welander type   726107008
  • Distal myopathy with anterior tibial onset   782675008
  • Distal myopathy with early respiratory muscle involvement   733490006  removed: 2019-07-31
  • Distal myopathy with posterior leg and anterior hand involvement   733489002
  • Distal nebulin myopathy   783148005
  • Finnish upper limb onset distal myopathy   763718009
  • KLHL9-related early-onset distal myopathy   763776004
  • Laing early-onset distal myopathy   764859001
  • Oculopharyngodistal myopathy   763829004
  • Progressive scapulohumeroperoneal distal myopathy   1217226000
  • Tibial muscular dystrophy   698846009
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
            Distal muscular dystrophy   58795000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Hereditary progressive muscular dystrophy   193225000
            Distal muscular dystrophy   58795000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Muscular dystrophy   73297009
          Muscular dystrophy not predominantly limb girdle in distribution   240070002
            Distal muscular dystrophy   58795000

ancestors
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