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Terminology chevron_right Concepts chevron_right 784340000

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784340000
The component that hold information about this concept.
Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)
Combined immunodeficiency due to il21r deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)

SCTID: 784340000, Primitive, Active


784340000|Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)|
  • en Combined immunodeficiency due to il21r deficiency
  • en Combined immunodeficiency due to interleukin 21 receptor deficiency
  • en Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)

784340000 |Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)|

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

3763682018 - Combined immunodeficiency due to IL21R deficiency (en) View

3763682018
en
Synonym (core metadata concept)
Combined immunodeficiency due to IL21R deficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3763683011 - Combined immunodeficiency due to interleukin 21 receptor deficiency (en) View

3763683011
en
Synonym (core metadata concept)
Combined immunodeficiency due to interleukin 21 receptor deficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3763681013 - Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder) (en) View

3763681013
en
Fully specified name (core metadata concept)
Combined immunodeficiency due to interleukin 21 receptor deficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

442459007 View

442459007
Combined immunodeficiency disease (disorder)
Combined immunodeficiency disease
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (1734b6f9-f2b4-5ce1-aa95-c9da72b8f074) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D81.8
TRUE
ALWAYS D81.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
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