CHILD syndrome   17608003

SNOMED CT code


SNOMED code17608003
nameCHILD syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder)
synonyms
  • Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
  • CHILD syndrome
  • CHILD (congenital hemidysplasia, ichthyosiform erythroderma, limb defects) syndrome
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
Finding siteSkin structure   39937001
OccurrenceCongenital   255399007
attributes - group3
InterpretsKeratinization   44138005
Has interpretationAbnormal   263654008
attributes - group2
OccurrenceCongenital   255399007
Finding siteLimb structure   66019005
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
parents
  • X-linked dominant hereditary disease   1162984000
  • Congenital anomaly of skin   199879009
  • Congenital ichthyosiform erythroderma   254156001
  • Disorder of lipid metabolism   267431006
  • Developmental hereditary disorder   363070008
  • Multiple malformation syndrome with limb defect as major feature   41443008
  • Congenital anomaly of limb   60475009
  • Inborn error of metabolism   86095007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              X-linked dominant hereditary disease   1162984000
                CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Congenital anomaly of integument   38164009
          Congenital anomaly of skin   199879009
            CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital ichthyosiform erythroderma   254156001
          CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of lipoprotein AND/OR lipid metabolism   48286001
          Disorder of lipid metabolism   267431006
            CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Multiple system malformation syndrome   82354003
              Multiple malformation syndrome with limb defect as major feature   41443008
                CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Disorder of limb   128605003
        Congenital anomaly of limb   60475009
          CHILD syndrome   17608003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          CHILD syndrome   17608003

ancestors
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