Keutel syndrome   724208006

SNOMED CT code


SNOMED code724208006
nameKeutel syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Keutel syndrome (disorder)
synonyms
  • Keutel syndrome
  • Pulmonic stenosis, brachytelephalangism, calcification of cartilage syndrome
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding sitePulmonary artery within lung   128260003
Associated morphologyStenosis   415582006
attributes - group4
OccurrenceCongenital   255399007
Associated morphologyPathologic calcification   18115005
Finding siteCartilage structure   771314001
Pathological processPathological developmental process   308490002
attributes - group2
OccurrenceCongenital   255399007
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
Finding siteFace structure   89545001
attributes - group3
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyAbnormally short growth   11182007
Finding siteDigit structure   82680008
parents
  • Multiple malformation syndrome with facial-limb defects as major feature   23359005
  • Chondrocalcinosis   239838005
  • Congenital peripheral pulmonary artery stenosis   286071000119109
  • Cardiovascular system hereditary disorder   363005004
  • Connective tissue hereditary disorder   363045008
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Brachydactyly   43476002
  • Congenital anomaly of cartilage   67988000
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
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
            Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Calcinosis   6595006
          Chondrocalcinosis   239838005
            Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Respiratory finding   106048009
      Lower respiratory tract finding   301226008
        Congenital anomaly of lower respiratory system   123654008
          Congenital anomaly of lung   47147007
            Congenital peripheral pulmonary artery stenosis   286071000119109
              Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Cardiovascular finding   106063007
      Disorder of cardiovascular system   49601007
        Cardiovascular system hereditary disorder   363005004
          Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Connective tissue hereditary disorder   363045008
          Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Deformity of limb   445144002
        Longitudinal deficiency of part of limb   716638009
          Brachydactyly   43476002
            Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Congenital connective tissue disorder   363039000
          Congenital anomaly of cartilage   67988000
            Keutel syndrome   724208006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Keutel syndrome   724208006

ancestors
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