Genodermatosis   239001006

SNOMED CT code


SNOMED code239001006
nameGenodermatosis
statusactive
date introduced2002-01-31
fully specified name(s)Genodermatosis (disorder)
synonymsGenodermatosis
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
Finding siteSkin structure   39937001
OccurrenceCongenital   255399007
parentsCongenital anomaly of skin   199879009
children
  • Acrokeratosis verruciformis of Hopf   400085009
  • Atrichia congenita   403798006
  • Chondrodysplasia punctata, X-linked dominant type   398958000
  • Congenital clubbing   276449002  removed: 2019-01-31
  • Congenital ichthyosis of skin   13059002
  • Congenital skin contracture   10624871000119109
  • Ectodermal dysplasia   8654005
  • Epidermolysis bullosa   61003004
  • Familial focal facial dermal dysplasia   254238008  removed: 2020-01-31
  • Familial multiple tumor syndrome   239003009  removed: 2019-07-31
  • Hereditary clubbing   239055005
  • Ichthyosis hystrix   67510007
  • Inherited cutaneous hyperpigmentation   239079007
  • Multiple benign annular creases of extremities   239053003
  • Pachydermoperiostosis of nail   223726008
  • Pachyonychia congenita syndrome   39427000
  • Palmoplantar keratoderma with clinodactyly syndrome   724224007
  • Reticulate pigmented anomaly of flexures   239054009
  • Rothmund-Thomson syndrome   69093006
hierarchies
a selection of possible paths
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
            Genodermatosis   239001006

ancestors
sorted most to least specific
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