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Terminology chevron_right Concepts chevron_right 1187119002

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Component

1187119002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary pediatric behçet-like disease (disorder)

Shortest Term

Behçet-like disease due to ha20

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

Hereditary pediatric behçet-like disease (disorder)

SCTID: 1187119002, Primitive, Active

1187119002|Hereditary pediatric behçet-like disease (disorder)|

en Behçet-like disease due to ha20
en Behçet-like disease due to haploinsufficiency of a20
en Hereditary paediatric behçet-like disease
en Hereditary pediatric behçet-like disease
en Hereditary pediatric behçet-like disease (disorder)

Expression

1187119002 |Hereditary pediatric behçet-like disease (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
58184002 |Recurrent disease (disorder)| + 
1290916005 |Haploinsufficiency of a20 (disorder)| + 
363138005 |Hereditary disorder of immune system (disorder)|
        { 116676008 |Associated morphology (attribute)| = 409774005 |Inflammatory morphology (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)|,
370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255227004 |Recurrent (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4669941019 - Behçet-like disease due to HA20 (en) View
4669941019	en	Synonym (core metadata concept)	Behçet-like disease due to HA20	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4669945011 - Behçet-like disease due to haploinsufficiency of A20 (en) View
4669945011	en	Synonym (core metadata concept)	Behçet-like disease due to haploinsufficiency of A20	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4669942014 - Hereditary paediatric Behçet-like disease (en) View
4669942014	en	Synonym (core metadata concept)	Hereditary paediatric Behçet-like disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4669943016 - Hereditary pediatric Behçet-like disease (en) View
4669943016	en	Synonym (core metadata concept)	Hereditary pediatric Behçet-like disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4669944010 - Hereditary pediatric Behçet-like disease (disorder) (en) View
4669944010	en	Fully specified name (core metadata concept)	Hereditary pediatric Behçet-like disease (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14963580025) - 1187119002 -> 128139000 (116680003) View
116680003 \|Is a (attribute)\|	128139000 \|Inflammatory disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14963584023) - 1187119002 -> 56019007 (116680003) View
116680003 \|Is a (attribute)\|	56019007 \|Systemic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14963592025) - 1187119002 -> 409774005 (116676008) View
116676008 \|Associated morphology (attribute)\|	409774005 \|Inflammatory morphology (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15779572020) - 1187119002 -> 1290916005 (116680003) View
116680003 \|Is a (attribute)\|	1290916005 \|Haploinsufficiency of a20 (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15779573026) - 1187119002 -> 363138005 (116680003) View
116680003 \|Is a (attribute)\|	363138005 \|Hereditary disorder of immune system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15779574021) - 1187119002 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15779575022) - 1187119002 -> 409774005 (116676008) View
116676008 \|Associated morphology (attribute)\|	409774005 \|Inflammatory morphology (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15779576023) - 1187119002 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14963579028) - 1187119002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14963585024) - 1187119002 -> 58184002 (116680003) View
116680003 \|Is a (attribute)\|	58184002 \|Recurrent disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14963587027) - 1187119002 -> 255227004 (263502005) View
263502005 \|Clinical course (attribute)\|	255227004 \|Recurrent (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1290916005 View
1290916005	Haploinsufficiency of a20 (disorder)	A20 haploinsufficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
58184002 View
58184002	Recurrent disease (disorder)	Recurrent disease	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
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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (64d08773-b4aa-508e-bd99-ee6e89733467) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D89.8	TRUE	ALWAYS D89.8 \| 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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