Epidermolysis bullosa simplex   67144006


SNOMED code67144006
nameEpidermolysis bullosa simplex
date introduced2002-01-31
fully specified name(s)Epidermolysis bullosa simplex (disorder)
synonymsEpidermolysis bullosa simplex
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteSkin structure   39937001
Associated morphologyEpidermolysis   85269007
parentsEpidermolysis bullosa   61003004
  • Autosomal dominant epidermolysis bullosa simplex   398170002
  • Autosomal recessive epidermolysis bullosa simplex   1156849001
  • Basal epidermolysis bullosa simplex   723163000
  • Epidermolysis bullosa simplex herpetiformis   254179000
  • Epidermolysis bullosa simplex of the hands and feet   367420002  removed: 2015-01-31
  • Epidermolysis bullosa simplex with hypodontia   254177003
  • Epidermolysis bullosa simplex with mottled pigmentation   254180002
  • Epidermolysis bullosa simplex with neuromuscular disease   254182005  removed: 2020-01-31
  • Epidermolysis simplex superficialis   254181003
  • Generalized epidermolysis bullosa simplex   254178008  removed: 2002-07-31
  • Generalized epidermolysis bullosa simplex   90496008
  • Suprabasal epidermolysis bullosa simplex   724840004
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
            Epidermolysis bullosa simplex   67144006

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