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Terminology chevron_right Concepts chevron_right 715864007

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Component

715864007

The component that hold information about this concept.

Fully Specified Name (FSN)

Non-wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

Shortest Term

Xơ gan liên quan đến đồng vô căn

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

Non-wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

SCTID: 715864007, Primitive, Active

715864007|Non-wilsonian hepatic copper toxicosis of infancy and childhood (disorder)|

vi Xơ gan liên quan đến đồng vô căn
en Idiopathic copper associated cirrhosis of liver
en Non-wilsonian hepatic copper toxicosis of infancy and childhood
en Non-wilsonian hepatic copper toxicosis of infancy and childhood (disorder)

Expression

715864007 |Non-wilsonian hepatic copper toxicosis of infancy and childhood (disorder)|
 <<< 89580002 |Cryptogenic cirrhosis (disorder)| + 
737204007 |Disorder of liver due to disorder of mineral metabolism (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 64770007 |Nodular regeneration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 57977008 |Chronic fibrosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        { 42752001 |Due to (attribute)| = 79886009 |Disorder of copper metabolism (disorder)| }
        { 246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)| }
        { 246454002 |Occurrence (attribute)| = 255398004 |Childhood (qualifier value)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
456621000003117 - xơ gan liên quan đến đồng vô căn (vi) View
456621000003117	vi	Synonym (core metadata concept)	xơ gan liên quan đến đồng vô căn	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3304659013 - Idiopathic copper associated cirrhosis of liver (en) View
3304659013	en	Synonym (core metadata concept)	Idiopathic copper associated cirrhosis of liver	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3303974016 - Non-Wilsonian hepatic copper toxicosis of infancy and childhood (en) View
3303974016	en	Synonym (core metadata concept)	Non-Wilsonian hepatic copper toxicosis of infancy and childhood	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
3304658017 - Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) (en) View
3304658017	en	Fully specified name (core metadata concept)	Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6557914029) - 715864007 -> 41969006 (116680003) View
116680003 \|Is a (attribute)\|	41969006 \|Idiopathic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6578802023) - 715864007 -> 19943007 (116680003) View
116680003 \|Is a (attribute)\|	19943007 \|Cirrhosis of liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13730097029) - 715864007 -> 89580002 (116680003) View
116680003 \|Is a (attribute)\|	89580002 \|Cryptogenic cirrhosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13741853021) - 715864007 -> 737204007 (116680003) View
116680003 \|Is a (attribute)\|	737204007 \|Disorder of liver due to disorder of mineral metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6578801027) - 715864007 -> 79886009 (42752001) View
42752001 \|Due to (attribute)\|	79886009 \|Disorder of copper metabolism (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6578803029) - 715864007 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6578804024) - 715864007 -> 255398004 (246454002) View
246454002 \|Occurrence (attribute)\|	255398004 \|Childhood (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9617201021) - 715864007 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6557920028) - 715864007 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6578805020) - 715864007 -> 64770007 (116676008) View
116676008 \|Associated morphology (attribute)\|	64770007 \|Nodular regeneration (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6578806021) - 715864007 -> 112674009 (116676008) View
116676008 \|Associated morphology (attribute)\|	112674009 \|Fibrosis (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6578807028) - 715864007 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9617202025) - 715864007 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621732029) - 715864007 -> 57977008 (116676008) View
116676008 \|Associated morphology (attribute)\|	57977008 \|Chronic fibrosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9621733023) - 715864007 -> 64770007 (116676008) View
116676008 \|Associated morphology (attribute)\|	64770007 \|Nodular regeneration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
89580002 View
89580002	Cryptogenic cirrhosis (disorder)	Idiopathic cirrhosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
737204007 View
737204007	Disorder of liver due to disorder of mineral metabolism (disorder)	Rối loạn gan do rối loạn chuyển hóa chất khoáng	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 (2d8bb865-5cd6-521e-9f1c-d07ac61ba35b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K74.6	TRUE	ALWAYS K74.6 \| 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)\|
ExtendedMap object (3b9aeea8-ff3a-5fce-bd1c-3b3e95f20b60) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.0	TRUE	ALWAYS E83.0	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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