Spondyloperipheral dysplasia   702339001

SNOMED CT code


SNOMED code702339001
nameSpondyloperipheral dysplasia
statusactive
date introduced2014-07-31
fully specified name(s)Spondyloperipheral dysplasia (disorder)
synonymsSpondyloperipheral dysplasia
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
OccurrenceCongenital   255399007
Finding siteBone structure   272673000
parents
  • Osteochondrodysplasia syndrome   105985007
  • Skeletal dysplasia   105986008
  • Autosomal dominant hereditary disorder   11164009
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Congenital anomaly of skeletal bone   8447006
childrenSpondyloperipheral dysplasia with short ulna syndrome   763886009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Osteochondrodysplasia syndrome   105985007
                Spondyloperipheral dysplasia   702339001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Disorder of skeletal system   88230002
          Skeletal dysplasia   105986008
            Spondyloperipheral dysplasia   702339001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Spondyloperipheral dysplasia   702339001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Spondyloperipheral dysplasia   702339001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Spondyloperipheral dysplasia   702339001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Spondyloperipheral dysplasia   702339001

ancestors
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