SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal dominant hereditary disorder  11164009

Autosomal dominant epidermolysis bullosa simplex  398170002

Weber-Cockayne syndrome   294705005

SNOMED CT code


SNOMED code294705005
nameWeber-Cockayne syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Dominant epidermolysis bullosa simplex, Weber-Cockayne type (disorder)
synonyms
  • Weber-Cockayne syndrome
  • Epidermolysis bullosa simplex of the hands AND/OR feet
  • DEBS-WC
  • Dominant epidermolysis bullosa simplex, Weber-Cockayne type
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyEpidermolysis   85269007
Finding siteSkin structure   39937001
parentsAutosomal dominant epidermolysis bullosa simplex   398170002
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
              Autosomal dominant epidermolysis bullosa simplex   398170002
                Weber-Cockayne syndrome   294705005

ancestors
sorted most to least specific
cpt crosswalks

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