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Terminology chevron_right Concepts chevron_right 1197361002

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1197361002
The component that hold information about this concept.
Autoimmune lymphoproliferative syndrome due to cytotoxic t-lymphocyte associated protein 4 haploinsufficiency (disorder)
Ctla-4 haploinsufficiency with autoimmune infiltration disease
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

Autoimmune lymphoproliferative syndrome due to cytotoxic t-lymphocyte associated protein 4 haploinsufficiency (disorder)

SCTID: 1197361002, Primitive, Active


1197361002|Autoimmune lymphoproliferative syndrome due to cytotoxic t-lymphocyte associated protein 4 haploinsufficiency (disorder)|
  • en Autoimmune lymphoproliferative syndrome due to ctla4 haploinsufficiency
  • en Autoimmune lymphoproliferative syndrome due to cytotoxic t-lymphocyte associated protein 4 haploinsufficiency
  • en Autoimmune lymphoproliferative syndrome due to cytotoxic t-lymphocyte associated protein 4 haploinsufficiency (disorder)
  • en Ctla-4 haploinsufficiency with autoimmune infiltration disease

1197361002 |Autoimmune lymphoproliferative syndrome due to cytotoxic t-lymphocyte associated protein 4 haploinsufficiency (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    702444009 |Autoimmune lymphoproliferative syndrome (disorder)| +
    85828009 |Autoimmune disease (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 414629003 |Lymphoproliferative disorder (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 56972008 |Lymphocyte (cell)|,
          370135005 |Pathological process (attribute)| = 263680009 |Autoimmune process (qualifier value)| }
Active

4696010012 - Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency (en) View

4696010012
en
Synonym (core metadata concept)
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

4696011011 - Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (en) View

4696011011
en
Synonym (core metadata concept)
Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

4696012016 - Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (disorder) (en) View

4696012016
en
Fully specified name (core metadata concept)
Autoimmune lymphoproliferative syndrome due to cytotoxic T-lymphocyte associated protein 4 haploinsufficiency (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

4696009019 - CTLA-4 haploinsufficiency with autoimmune infiltration disease (en) View

4696009019
en
Synonym (core metadata concept)
CTLA-4 haploinsufficiency with autoimmune infiltration disease
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (15028769027) - 1197361002 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15028770026) - 1197361002 -> 702444009 (116680003) View

116680003 |Is a (attribute)|
702444009 |Autoimmune lymphoproliferative syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15028771027) - 1197361002 -> 56972008 (363698007) View

363698007 |Finding site (attribute)|
56972008 |Lymphocyte (cell)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15028772023) - 1197361002 -> 414629003 (116676008) View

116676008 |Associated morphology (attribute)|
414629003 |Lymphoproliferative disorder (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15028774024) - 1197361002 -> 85828009 (116680003) View

116680003 |Is a (attribute)|
85828009 |Autoimmune disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15028775020) - 1197361002 -> 263680009 (370135005) View

370135005 |Pathological process (attribute)|
263680009 |Autoimmune process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

702444009 View

702444009
Autoimmune lymphoproliferative syndrome (disorder)
Canale-smith syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

85828009 View

85828009
Autoimmune disease (disorder)
Bệnh tự miễn
900000000000073002 |Sufficiently defined by necessary conditions 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 (dbd769b1-6437-5f69-9523-b8a3727481a7) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D84.8
TRUE
ALWAYS D84.8 | 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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