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Terminology chevron_right Concepts chevron_right 234640004

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234640004
The component that hold information about this concept.
18-p syndrome with associated immunodeficiency (disorder)
Immunodeficiency associated with 18p syndrome
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

18-p syndrome with associated immunodeficiency (disorder)

SCTID: 234640004, Primitive, Active


234640004|18-p syndrome with associated immunodeficiency (disorder)|
  • en 18-p syndrome with associated immunodeficiency
  • en 18-p syndrome with associated immunodeficiency (disorder)
  • en Immunodeficiency associated with 18p syndrome

234640004 |18-p syndrome with associated immunodeficiency (disorder)|

<<< 234632005 |Immunodeficiency associated with chromosomal abnormality (disorder)| :
        { 47429007 |Associated with (attribute)| = 409709004 |Chromosomal disorder (disorder)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

351583012 - 18-p syndrome with associated immunodeficiency (en) View

351583012
en
Synonym (core metadata concept)
18-p syndrome with associated immunodeficiency
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

622987012 - 18-p syndrome with associated immunodeficiency (disorder) (en) View

622987012
en
Fully specified name (core metadata concept)
18-p syndrome with associated immunodeficiency (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2532304011 - Immunodeficiency associated with 18p syndrome (en) View

2532304011
en
Synonym (core metadata concept)
Immunodeficiency associated with 18p syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

234632005 View

234632005
Immunodeficiency associated with chromosomal abnormality (disorder)
Immunodeficiency associated with chromosomal abnormality
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (69e949e0-649f-55c0-ba80-2a93f9248a53) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D82.8
TRUE
ALWAYS D82.8
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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