Papillon-Lefèvre syndrome   40158001

SNOMED CT code


SNOMED code40158001
namePapillon-Lefèvre syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Papillon-Lefèvre syndrome (disorder)
synonyms
  • Papillon-Lefevre syndrome
  • Papillon-Lefèvre syndrome
  • Juvenile periodontosis with hyperkeratosis
attributes - group3
Pathological processPathological developmental process   308490002
Finding siteSkin structure of palmar area of hand   70887009
Associated morphologyHyperkeratosis   26996000
OccurrenceCongenital   255399007
attributes - group2
OccurrenceCongenital   255399007
Associated morphologyHyperkeratosis   26996000
Pathological processPathological developmental process   308490002
Finding siteSkin structure of sole of foot   37136002
attributes - group4
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
Finding siteAlveolar process   129143008
OccurrenceCongenital   255399007
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
OccurrenceCongenital   255399007
Finding siteEctoderm structure   63206006
parents
  • Alveolar bone loss   109706009
  • Congenital anomaly of foot   253966001
  • Congenital anomaly of face bones   32003007
  • Congenital anomaly of the hand   34111000
  • Hereditary disorder of musculoskeletal system   363212003
  • Hereditary diffuse palmoplantar keratoderma   400123002
  • Autosomal recessive hereditary disorder   85995004
  • Ectodermal dysplasia   8654005
  • Congenital anomaly of jaw   95473006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of head   118934005
          Disorder of face   118930001
            Disorder of facial bone   128225009
              Alveolar bone loss   109706009
                Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Congenital abnormality of lower limb and pelvic girdle   253937004
          Congenital anomaly of lower limb   84773003
            Congenital anomaly of foot   253966001
              Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of head   118934005
          Disorder of face   118930001
            Disorder of facial bone   128225009
              Congenital anomaly of face bones   32003007
                Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of extremity   128605003
          Congenital anomaly of limb   60475009
            Congenital anomaly of upper limb   66510004
              Congenital anomaly of the hand   34111000
                Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Musculoskeletal finding   106028002
        Disorder of musculoskeletal system   928000
          Hereditary disorder of musculoskeletal system   363212003
            Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Integumentary system finding   106077005
        Disorder of integument   128598002
          Hereditary disorder of the integument   363185004
            Hereditary palmoplantar keratoderma   239066003
              Hereditary diffuse palmoplantar keratoderma   400123002
                Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital ectodermal defect   254154003
            Ectodermal dysplasia   8654005
              Papillon-Lefèvre syndrome   40158001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of head   118934005
          Disorder of face   118930001
            Disorder of jaw   37156001
              Congenital anomaly of jaw   95473006
                Papillon-Lefèvre syndrome   40158001

ancestors
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