Schinzel-Giedion syndrome   18899000

SNOMED CT code


SNOMED code18899000
nameSchinzel-Giedion syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Schinzel-Giedion syndrome (disorder)
synonymsSchinzel-Giedion syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteEctoderm structure   63206006
Associated morphologyDysplasia   25723000
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteNail unit structure   770802007
OccurrenceCongenital   255399007
attributes - group4
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteHair structure   386045008
Associated morphologyMorphologically abnormal structure   49755003
attributes - group3
Pathological processPathological developmental process   308490002
Finding siteTooth structure   38199008
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
parents
  • Hereditary disorder of tooth   1148766007
  • Ectodermal dysplasia with hair-tooth-nail defects   239015008
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of the integument   363185004
  • Genetic disorder of nail   402775007
  • Multiple malformation syndrome with unusual brain and/or neuromuscular findings   64162006
  • Hereditary cancer-predisposing syndrome   699346009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Hereditary disorder of tooth   1148766007
            Schinzel-Giedion syndrome   18899000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of embryonic structure   609521009
        Congenital ectodermal defect   254154003
          Ectodermal dysplasia   8654005
            Ectodermal dysplasia with hair-tooth defects   239027006
              Ectodermal dysplasia with hair-tooth-nail defects   239015008
                Schinzel-Giedion syndrome   18899000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Schinzel-Giedion syndrome   18899000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Schinzel-Giedion syndrome   18899000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic disorder of nail   402775007
          Schinzel-Giedion syndrome   18899000

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 unusual brain and/or neuromuscular findings   64162006
                Schinzel-Giedion syndrome   18899000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary cancer-predisposing syndrome   699346009
            Schinzel-Giedion syndrome   18899000

ancestors
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