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Terminology chevron_right Concepts chevron_right 1363572000

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1363572000
The component that hold information about this concept.
Combined immunodeficiency due to forkhead box n1 haploinsufficiency (disorder)
Combined immunodeficiency due to foxn1 haploinsufficiency
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 forkhead box n1 haploinsufficiency (disorder)

SCTID: 1363572000, Primitive, Active


1363572000|Combined immunodeficiency due to forkhead box n1 haploinsufficiency (disorder)|
  • en Combined immunodeficiency due to forkhead box n1 haploinsufficiency
  • en Combined immunodeficiency due to forkhead box n1 haploinsufficiency (disorder)
  • en Combined immunodeficiency due to foxn1 haploinsufficiency

1363572000 |Combined immunodeficiency due to forkhead box n1 haploinsufficiency (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    442459007 |Combined immunodeficiency disease (disorder)| :
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
Active

5449741017 - Combined immunodeficiency due to forkhead box N1 haploinsufficiency (en) View

5449741017
en
Synonym (core metadata concept)
Combined immunodeficiency due to forkhead box N1 haploinsufficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

5449742012 - Combined immunodeficiency due to forkhead box N1 haploinsufficiency (disorder) (en) View

5449742012
en
Fully specified name (core metadata concept)
Combined immunodeficiency due to forkhead box N1 haploinsufficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

5449743019 - Combined immunodeficiency due to FOXN1 haploinsufficiency (en) View

5449743019
en
Synonym (core metadata concept)
Combined immunodeficiency due to FOXN1 haploinsufficiency
900000000000020002 |Only initial character 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

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (73d62e2e-ca7b-53d3-a6e2-d6a0cca95b86) 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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