Ectodermal dysplasia with hair-tooth-nail defects   239015008

SNOMED CT code


SNOMED code239015008
nameEctodermal dysplasia with hair-tooth-nail defects
statusactive
date introduced2002-01-31
fully specified name(s)Ectodermal dysplasia with hair-tooth-nail defects (disorder)
synonymsEctodermal dysplasia with hair-tooth-nail defects
attributes - group2
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteTooth structure   38199008
OccurrenceCongenital   255399007
attributes - group1
Pathological processPathological developmental process   308490002
Finding siteEctoderm structure   63206006
OccurrenceCongenital   255399007
Associated morphologyDysplasia   25723000
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteHair structure   386045008
OccurrenceCongenital   255399007
attributes - group4
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
Finding siteNail unit structure   770802007
OccurrenceCongenital   255399007
parents
  • Ectodermal dysplasia with hair-tooth defects   239027006
  • Ectodermal dysplasia with hair-nail defect   239035009
  • Ectodermal dysplasia with tooth-nail defects   239040001
children
  • Arthrogryposis and ectodermal dysplasia syndrome   786039009
  • Chondroectodermal dysplasia   62501005
  • Dermo-odonto dysplasia   721091003
  • Dermodental dysplasia   239022000
  • Dwarfism, alopecia, pseudoanodontia, cutis laxa   239025003
  • Ectodermal dysplasia trichoodontoonychial type   734018003
  • Ectodermal dysplasia with hair-tooth-nail-sweating defect   239006001
  • Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome   1279835008
  • Ectodermal dysplasia, syndactyly and pili torti   239024004
  • Fried's tooth and nail syndrome   239020008
  • Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome   763658004
  • Incontinentia pigmenti syndrome   367520004
  • Oculotrichodysplasia   722062004
  • Odonto onycho dysplasia with alopecia syndrome   763828007
  • Odonto-onychial dysplasia with alopecia   239019002
  • Odonto-onycho-dermal dysplasia   403762003
  • Salamon's syndrome   239023005
  • Schinzel-Giedion syndrome   18899000
  • Schoepf-Schulz-Passage syndrome   239018005
  • Tricho-dento-osseous syndrome   38993008
  • Tricho-onychodental dysplasia   239014007
  • Trichodermodysplasia and dental alterations syndrome   763620003
  • Trichoodontoonychial dysplasia   766813000
hierarchies
a selection of possible paths
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

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
            Congenital anomaly of hair   65033000
              Ectodermal dysplasia with hair-nail defect   239035009
                Ectodermal dysplasia with hair-tooth-nail defects   239015008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental abnormality of nail   238715009
          Congenital anomaly of nail   35964007
            Ectodermal dysplasia with nail defect   239046007
              Ectodermal dysplasia with tooth-nail defects   239040001
                Ectodermal dysplasia with hair-tooth-nail defects   239015008

ancestors
sorted most to least specific
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