SNOMED CT Concept  138875005

Clinical finding  404684003

Integumentary system finding  106077005

Disorder of integument  128598002

Hereditary disorder of the integument  363185004

Epidermolysis bullosa  61003004

Dystrophic epidermolysis bullosa  254185007

Generalized dystrophic epidermolysis bullosa   254188009

SNOMED CT code


SNOMED code254188009
nameGeneralized dystrophic epidermolysis bullosa
statusactive
date introduced2002-01-31
fully specified name(s)Generalized dystrophic epidermolysis bullosa (disorder)
synonyms
  • Generalized dystrophic epidermolysis bullosa
  • Generalised dystrophic epidermolysis bullosa
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyEpidermolysis   85269007
OccurrenceCongenital   255399007
Finding siteSkin structure   39937001
parentsDystrophic epidermolysis bullosa   254185007
children
  • Autosomal dominant generalized dystrophic epidermolysis bullosa   1231284001
  • Dominant dystrophic epidermolysis bullosa, albopapular type   75875004
  • Dystrophic epidermolysis bullosa inverse type   403809003
  • Epidermolysis bullosa pruriginosa   403810008
  • Generalized recessive dystrophic epidermolysis bullosa mitis   254189001
  • Generalized recessive non-mutilating dystrophic epidermolysis bullosa   403808006
  • Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type   725407006
  • Severe generalized recessive dystrophic epidermolysis bullosa   723716009
  • Transient bullous dermolysis of newborn   723553000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Epidermolysis bullosa   61003004
            Dystrophic epidermolysis bullosa   254185007
              Generalized dystrophic epidermolysis bullosa   254188009

ancestors
sorted most to least specific
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