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Terminology chevron_right Concepts chevron_right 733206005

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The component that hold information about this concept.
Erythroderma in infancy (disorder)
Erythroderma in infancy
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Erythroderma in infancy (disorder)

SCTID: 733206005, Defined, Active


733206005|Erythroderma in infancy (disorder)|
  • en Erythroderma in infancy
  • en Erythroderma in infancy (disorder)

733206005 |Erythroderma in infancy (disorder)|

=== 399992009 |Erythroderma (disorder)| +
    239091003 |Dermatosis of infancy (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 70819003 |Erythema (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 39937001 |Skin structure (body structure)|,
          246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
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