Cutis laxa, autosomal dominant   111388003

SNOMED CT code


SNOMED code111388003
nameCutis laxa, autosomal dominant
statusactive
date introduced2002-01-31
fully specified name(s)Cutis laxa, autosomal dominant (disorder)
synonymsCutis laxa, autosomal dominant
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteConnective tissue structure   21793004
attributes - group2
Finding siteSkin structure   39937001
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
              Cutis laxa, autosomal dominant   111388003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Congenital connective tissue disorder   363039000
          Inherited cutis laxa   254220005
            Cutis laxa, autosomal dominant   111388003

ancestors
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