Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT code


SNOMED code724069009
namePatterson Stevenson Fontaine syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Patterson Stevenson Fontaine syndrome (disorder)
synonyms
  • Patterson Stevenson Fontaine syndrome
  • Split foot deformity with mandibulofacial dysostosis syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteBone structure of extremity   48566001
Associated morphologyDysplasia   25723000
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
OccurrenceCongenital   255399007
Finding siteBone structure of face   91397008
parents
  • Dysostosis   109420003
  • Autosomal dominant hereditary disorder   11164009
  • Multiple malformation syndrome with facial-limb defects as major feature   23359005
  • Congenital anomaly of face bones   32003007
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Lesion of face   767811005
  • Congenital dysplasia of limb   88631000119105
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Dysostosis   109420003
              Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Patterson Stevenson Fontaine syndrome   724069009

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
            Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Bone finding   118953000
        Facial bone finding   248398006
          Disorder of facial bone   128225009
            Congenital anomaly of face bones   32003007
              Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Disorder of face   118930001
          Lesion of face   767811005
            Patterson Stevenson Fontaine syndrome   724069009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          Congenital dysplasia of limb   88631000119105
            Patterson Stevenson Fontaine syndrome   724069009

ancestors
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