Larsen syndrome   63387002

SNOMED CT code


SNOMED code63387002
nameLarsen syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Larsen syndrome (disorder)
synonymsLarsen syndrome
attributes - group2
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteBone structure   272673000
Associated morphologyDysplasia   25723000
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteFace structure   89545001
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteLimb structure   66019005
Associated morphologyMorphologically abnormal structure   49755003
attributes - group4
Associated morphologyDislocation   87642003
Finding siteJoint structure of multiple body sites   773190007
attributes - group5
Clinical courseProgressive   255314001
attributes - group6
Due toSpontaneous event   789750003
parents
  • Autosomal dominant hereditary disorder   11164009
  • Injury of face   125593007
  • Multiple malformation syndrome with facial-limb defects as major feature   23359005
  • Multiple dislocations with dysplasia   254098000
  • Bone injury   284003005
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Congenital anomaly of skeletal bone   8447006
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
              Larsen syndrome   63387002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Injury of face   125593007
            Larsen syndrome   63387002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          Multiple malformation syndrome with facial-limb defects as major feature   23359005
            Larsen syndrome   63387002

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
              Larsen syndrome   63387002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Traumatic or non-traumatic injury   417163006
        Injury of musculoskeletal system   105606008
          Bone injury   284003005
            Larsen syndrome   63387002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Larsen syndrome   63387002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Larsen syndrome   63387002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Larsen syndrome   63387002

ancestors
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