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Terminology chevron_right Concepts chevron_right 1351781002

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The component that hold information about this concept.
Autosomal recessive combined immunodeficiency due to bcl10 immune signaling adaptor mutation (disorder)
Autosomal recessive combined immunodeficiency due to bcl10 mutation
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Autosomal recessive combined immunodeficiency due to bcl10 immune signaling adaptor mutation (disorder)

SCTID: 1351781002, Primitive, Active


1351781002|Autosomal recessive combined immunodeficiency due to bcl10 immune signaling adaptor mutation (disorder)|
  • en Autosomal recessive combined immunodeficiency due to bcl10 deficiency
  • en Autosomal recessive combined immunodeficiency due to bcl10 immune signaling adaptor mutation
  • en Autosomal recessive combined immunodeficiency due to bcl10 immune signaling adaptor mutation (disorder)
  • en Autosomal recessive combined immunodeficiency due to bcl10 mutation

1351781002 |Autosomal recessive combined immunodeficiency due to bcl10 immune signaling adaptor mutation (disorder)|

<<< 442459007 |Combined immunodeficiency disease (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| :
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
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