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Terminology chevron_right Concepts chevron_right 702444009

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Component

702444009

The component that hold information about this concept.

Fully Specified Name (FSN)

Autoimmune lymphoproliferative syndrome (disorder)

Shortest Term

Canale-smith syndrome

Definition Status

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

Summary

Autoimmune lymphoproliferative syndrome (disorder)

SCTID: 702444009, Primitive, Active

702444009|Autoimmune lymphoproliferative syndrome (disorder)|

en Alps - autoimmune lymphoproliferative syndrome
en Autoimmune lymphoproliferative syndrome
en Autoimmune lymphoproliferative syndrome (disorder)
en Canale-smith syndrome

Expression

702444009 |Autoimmune lymphoproliferative syndrome (disorder)|
 <<< 277466009 |Lymphoproliferative disorder (disorder)| + 
414027002 |Disorder of hematopoietic structure (disorder)| + 
414030009 |Disorder of immune structure (disorder)| + 
58606001 |Primary immune deficiency disorder (disorder)| + 
1899006 |Autosomal hereditary disorder (disorder)| + 
363138005 |Hereditary disorder of immune system (disorder)| + 
699346009 |Hereditary cancer-predisposing syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 414629003 |Lymphoproliferative disorder (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 56972008 |Lymphocyte (cell)|,
370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5286163018 - ALPS - autoimmune lymphoproliferative syndrome (en) View
5286163018	en	Synonym (core metadata concept)	ALPS - autoimmune lymphoproliferative syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2995326018 - Autoimmune lymphoproliferative syndrome (en) View
2995326018	en	Synonym (core metadata concept)	Autoimmune lymphoproliferative syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2995459016 - Autoimmune lymphoproliferative syndrome (disorder) (en) View
2995459016	en	Fully specified name (core metadata concept)	Autoimmune lymphoproliferative syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2995703010 - Canale-Smith syndrome (en) View
2995703010	en	Synonym (core metadata concept)	Canale-Smith syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12438148026) - 702444009 -> 277606000 (116680003) View
116680003 \|Is a (attribute)\|	277606000 \|Lymphoreticular tumor (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12438149023) - 702444009 -> 109958007 (116680003) View
116680003 \|Is a (attribute)\|	109958007 \|Hematologic neoplasm of uncertain behavior (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12438150023) - 702444009 -> 414823004 (116680003) View
116680003 \|Is a (attribute)\|	414823004 \|Neoplasm affecting hematopoietic structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12438151022) - 702444009 -> 84631004 (116676008) View
116676008 \|Associated morphology (attribute)\|	84631004 \|Lymphoproliferative disease, no icd-o subtype (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13891543029) - 702444009 -> 277466009 (116680003) View
116680003 \|Is a (attribute)\|	277466009 \|Lymphoproliferative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13891544024) - 702444009 -> 414027002 (116680003) View
116680003 \|Is a (attribute)\|	414027002 \|Disorder of hematopoietic structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13891545020) - 702444009 -> 414629003 (116676008) View
116676008 \|Associated morphology (attribute)\|	414629003 \|Lymphoproliferative disorder (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968700021) - 702444009 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968701020) - 702444009 -> 3239007 (116680003) View
116680003 \|Is a (attribute)\|	3239007 \|Lymphocyte disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12436713022) - 702444009 -> 363138005 (116680003) View
116680003 \|Is a (attribute)\|	363138005 \|Hereditary disorder of immune system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12437009026) - 702444009 -> 414030009 (116680003) View
116680003 \|Is a (attribute)\|	414030009 \|Disorder of immune structure (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12438077027) - 702444009 -> 58606001 (116680003) View
116680003 \|Is a (attribute)\|	58606001 \|Primary immune deficiency disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12438078021) - 702444009 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12438079029) - 702444009 -> 56972008 (363698007) View
363698007 \|Finding site (attribute)\|	56972008 \|Lymphocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12438152026) - 702444009 -> 699346009 (116680003) View
116680003 \|Is a (attribute)\|	699346009 \|Hereditary cancer-predisposing syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11172163028) - 702444009 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5046358023) - 702444009 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
699346009 View
699346009	Hereditary cancer-predisposing syndrome (disorder)	Hereditary neoplastic syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
414027002 View
414027002	Disorder of hematopoietic structure (disorder)	Rối loạn cấu trúc tạo máu	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
414030009 View
414030009	Disorder of immune structure (disorder)	Disorder of immune structure	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
277466009 View
277466009	Lymphoproliferative disorder (disorder)	Bệnh tăng sinh mô bạch huyết	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1899006 View
1899006	Autosomal hereditary disorder (disorder)	Autosomal hereditary disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
58606001 View
58606001	Primary immune deficiency disorder (disorder)	Primary immunodeficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363138005 View
363138005	Hereditary disorder of immune system (disorder)	Hereditary disorder of immune system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1197361002 View
1197361002	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)\|	True
1197362009 View
1197362009	Signal transducer and activator of transcription 3-related early-onset multisystem autoimmune disease (disorder)	Stat3-related early-onset multisystem autoimmune disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (b05a23f3-1b7b-5fc9-a160-bd21bdbf1b01) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D72.8	TRUE	ALWAYS D72.8	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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