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Terminology chevron_right Concepts chevron_right 79468000

Production
The component that hold information about this concept.
Familial benign pemphigus (disorder)
Hailey hailey disease
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Familial benign pemphigus (disorder)

SCTID: 79468000, Primitive, Active


79468000|Familial benign pemphigus (disorder)|
  • en Benign familial chronic pemphigus
  • en Familial benign chronic pemphigus
  • en Familial benign pemphigus
  • en Familial benign pemphigus (disorder)
  • en Hailey hailey disease
  • en Hailey-hailey disease

79468000 |Familial benign pemphigus (disorder)|

<<< 254214009 |Inherited disorder of keratinization (disorder)| +
    128236002 |Chronic disease of skin (disorder)| +
    11164009 |Autosomal dominant hereditary disorder (disorder)| +
    823996003 |Blister of skin (disorder)| +
    1251371002 |Acantholysis of skin (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 339008 |Blister (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 43327007 |Acantholysis (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)| }
        { 263502005 |Clinical course (attribute)| = 90734009 |Chronic (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 44138005 |Keratinization, function (observable entity)| }
Active
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