Acroosteolysis, keloid-like lesions, premature aging syndrome   776417008

SNOMED CT code


SNOMED code776417008
nameAcroosteolysis, keloid-like lesions, premature aging syndrome
statusactive
date introduced2019-01-31
fully specified name(s)Acroosteolysis, keloid-like lesions, premature aging syndrome (disorder)
synonyms
  • Acroosteolysis, keloid-like lesions, premature ageing syndrome
  • Acroosteolysis, keloid-like lesions, premature aging syndrome
  • Premature aging syndrome, Penttinen type
  • Premature ageing syndrome Penttinen type
attributes - group1
OccurrenceCongenital   255399007
Finding siteSkin structure   39937001
attributes - group2
Finding siteBone structure   272673000
OccurrenceCongenital   255399007
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Acroosteolysis, keloid-like lesions, premature aging syndrome   776417008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Hereditary acroosteolysis   254148004
            Acroosteolysis, keloid-like lesions, premature aging syndrome   776417008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Premature aging syndrome   399959003
            Acroosteolysis, keloid-like lesions, premature aging syndrome   776417008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Metabolic bone disease   50279003
          Acroosteolysis, keloid-like lesions, premature aging syndrome   776417008

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