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Terminology chevron_right Concepts chevron_right 1362020006

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The component that hold information about this concept.
Hyperimmunoglobulin m syndrome type 3 (disorder)
Hyperimmunoglobulin m syndrome type 3
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Hyperimmunoglobulin m syndrome type 3 (disorder)

SCTID: 1362020006, Primitive, Active


1362020006|Hyperimmunoglobulin m syndrome type 3 (disorder)|
  • en Autosomal recessive combined immunodeficiency due to cd40 mutation
  • en Higm3 - hyperimmunoglobulin m syndrome type 3
  • en Hyper-igm syndrome due to cd40 deficiency
  • en Hyperimmunoglobulin m syndrome type 3
  • en Hyperimmunoglobulin m syndrome type 3 (disorder)

1362020006 |Hyperimmunoglobulin m syndrome type 3 (disorder)|

<<< 403836001 |Autosomal recessive hyper- immunoglobulin m syndrome (disorder)| +
    783248004 |Hyperimmunoglobulin m syndrome with susceptibility to opportunistic infection (disorder)| :
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
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