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Terminology chevron_right Concepts chevron_right 58034007

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The component that hold information about this concept.
Congenital hypergammaglobulinemia (disorder)
Hypergammaglobulinemia, nos
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital hypergammaglobulinemia (disorder)

SCTID: 58034007, Primitive, Active


58034007|Congenital hypergammaglobulinemia (disorder)|
  • en Congenital hypergammaglobulinaemia
  • en Congenital hypergammaglobulinemia
  • en Congenital hypergammaglobulinemia (disorder)

58034007 |Congenital hypergammaglobulinemia (disorder)|

<<< 36138009 |Congenital immunodeficiency disease (disorder)| :
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
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