Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

SNOMED CT code


SNOMED code766820007
nameSpondyloepimetaphyseal dysplasia with multiple dislocations
statusactive
date introduced2018-07-31
fully specified name(s)Spondyloepimetaphyseal dysplasia with multiple dislocations (disorder)
synonyms
  • Spondyloepimetaphyseal dysplasia with multiple dislocations
  • Spondyloepimetaphyseal dysplasia with joint laxity type 2
  • Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic type
  • Spondyloepimetaphyseal dysplasia with joint laxity Hall type
  • Spondyloepimetaphyseal dysplasia with multiple dislocations Hall type
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
Finding siteBone structure   272673000
OccurrenceCongenital   255399007
attributes - group2
Finding siteJoint structure of multiple body sites   773190007
Associated morphologyDislocation   87642003
attributes - group3
Clinical courseProgressive   255314001
attributes - group4
Due toSpontaneous event   789750003
attributes - group5
InterpretsHeight / growth measure   271603002
parents
  • Autosomal dominant hereditary disorder   11164009
  • Spondyloepimetaphyseal disorder   254062008
  • Multiple dislocations with dysplasia   254098000
  • Bone injury   284003005
  • 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
              Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Metaphyseal chondrodysplasia   28681006
              Spondyloepimetaphyseal disorder   254062008
                Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chronic disease   27624003
        Chronic disease of musculoskeletal system   128237006
          Chronic arthropathy   38850007
            Multiple dislocations with dysplasia   254098000
              Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Traumatic or non-traumatic injury   417163006
        Injury of musculoskeletal system   105606008
          Bone injury   284003005
            Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Spondyloepimetaphyseal dysplasia with multiple dislocations   766820007

ancestors
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