Lelis syndrome   719429003

SNOMED CT code


SNOMED code719429003
nameLelis syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Ectodermal dysplasia with acanthosis nigricans syndrome (disorder)
synonyms
  • Lelis syndrome
  • Ectodermal dysplasia with acanthosis nigricans syndrome
attributes - group2
Pathological processPathological developmental process   308490002
Finding siteSkin structure   39937001
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
attributes - group3
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
OccurrenceCongenital   255399007
Finding siteEctoderm structure   63206006
attributes - group1
Has interpretationAbnormal   263654008
InterpretsKeratinization   44138005
parents
  • Inherited disorder of keratinization   254214009
  • Developmental hereditary disorder   363070008
  • Acanthosis nigricans   402599005
  • Autosomal recessive hereditary disorder   85995004
  • Ectodermal dysplasia   8654005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Disorder of keratinization   277905003
          Inherited disorder of keratinization   254214009
            Lelis syndrome   719429003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Lelis syndrome   719429003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Disorder of keratinization   277905003
          Acanthosis nigricans   402599005
            Lelis syndrome   719429003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Lelis syndrome   719429003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of embryonic structure   609521009
        Congenital ectodermal defect   254154003
          Ectodermal dysplasia   8654005
            Lelis syndrome   719429003

ancestors
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