Erythrokeratodermia variabilis   70041004

SNOMED CT code


SNOMED code70041004
nameErythrokeratodermia variabilis
statusactive
date introduced2002-01-31
fully specified name(s)Erythrokeratodermia variabilis (disorder)
synonyms
  • Erythrokeratodermia variabilis
  • Congenital poikiloderma
  • Mendes da Costa syndrome
attributes - group1
Finding siteEntire skin   181469002
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyHyperkeratosis   26996000
attributes - group2
Has interpretationAbnormal   263654008
InterpretsKeratinization   44138005
parents
  • Congenital ichthyosis of skin   13059002
  • Autosomal hereditary disorder   1899006
  • Congenital keratoderma   6874009
childrenMalignant atrophic papulosis   11131009  removed: 2003-07-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Skin finding   106076001
        Rough skin   816995008
          Congenital ichthyosis of skin   13059002
            Erythrokeratodermia variabilis   70041004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Erythrokeratodermia variabilis   70041004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital keratoderma   6874009
          Erythrokeratodermia variabilis   70041004

ancestors
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