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Terminology chevron_right Concepts chevron_right 16894671000119102

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The component that hold information about this concept.
Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance (disorder)
Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance (disorder)

SCTID: 16894671000119102, Defined, Active


16894671000119102|Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance (disorder)|
  • en Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance
  • en Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance (disorder)

16894671000119102 |Immunoglobulin g deficiency due to monoclonal gammopathy of undetermined significance (disorder)|

=== 414030009 |Disorder of immune structure (disorder)| +
    12631000119106 |Immunoglobulin g deficiency (disorder)| :
        { 363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        { 42752001 |Due to (attribute)| = 277577000 |Monoclonal gammopathy of uncertain significance (disorder)| }
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