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Terminology chevron_right Concepts chevron_right 61003004

Production
The component that hold information about this concept.
Epidermolysis bullosa (disorder)
Fox disease
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Epidermolysis bullosa (disorder)

SCTID: 61003004, Primitive, Active


61003004|Epidermolysis bullosa (disorder)|
  • en Acantholysis bullosa
  • en Acanthosis bullosa
  • en Bullous recurrent eruption
  • en Dermatitis bullosa hereditaria
  • en Epidermolysis bullosa
  • en Epidermolysis bullosa (disorder)
  • en Keratolysis bullosa hereditaria
  • en Fox disease
  • en Eb - epidermolysis bullosa

61003004 |Epidermolysis bullosa (disorder)|

<<< 363185004 |Hereditary disorder of the integument (disorder)| +
    239001006 |Genodermatosis (disorder)| +
    396325007 |Degenerative skin disorder (disorder)| +
    363070008 |Developmental hereditary disorder (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 85269007 |Epidermolysis (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
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