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Terminology chevron_right Concepts chevron_right 723443003

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723443003
The component that hold information about this concept.
Neutrophil immunodeficiency syndrome (disorder)
Neutrophil immunodeficiency 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

Neutrophil immunodeficiency syndrome (disorder)

SCTID: 723443003, Primitive, Active


723443003|Neutrophil immunodeficiency syndrome (disorder)|
  • en Neutrophil immunodeficiency syndrome
  • en Neutrophil immunodeficiency syndrome (disorder)

723443003 |Neutrophil immunodeficiency syndrome (disorder)|

<<< 234632005 |Immunodeficiency associated with chromosomal abnormality (disorder)| +
    402794002 |Heritable disorder of neutrophil function (disorder)| :
        { 42752001 |Due to (attribute)| = 409709004 |Chromosomal disorder (disorder)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
Active

3424635011 - Neutrophil immunodeficiency syndrome (en) View

3424635011
en
Synonym (core metadata concept)
Neutrophil immunodeficiency syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3424634010 - Neutrophil immunodeficiency syndrome (disorder) (en) View

3424634010
en
Fully specified name (core metadata concept)
Neutrophil immunodeficiency syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (6818171026) - 723443003 -> 409709004 (42752001) View

42752001 |Due to (attribute)|
409709004 |Chromosomal disorder (disorder)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6818174023) - 723443003 -> 91689009 (363698007) View

363698007 |Finding site (attribute)|
91689009 |Body system structure (body structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11171364029) - 723443003 -> 769247005 (370135005) View

370135005 |Pathological process (attribute)|
769247005 |Abnormal immune process (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6818175024) - 723443003 -> 106182000 (363705008) View

363705008 |Has definitional manifestation (attribute)|
106182000 |Immune system finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6818172022) - 723443003 -> 234632005 (116680003) View

116680003 |Is a (attribute)|
234632005 |Immunodeficiency associated with chromosomal abnormality (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6818173028) - 723443003 -> 402794002 (116680003) View

116680003 |Is a (attribute)|
402794002 |Heritable disorder of neutrophil function (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

402794002 View

402794002
Heritable disorder of neutrophil function (disorder)
Heritable disorder of neutrophil function
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
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 (67f09157-06d3-5475-b840-cf81a8a9446d) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D71
TRUE
ALWAYS D71 | 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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