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Terminology chevron_right Concepts chevron_right 195025008

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Component

195025008

The component that hold information about this concept.

Fully Specified Name (FSN)

Cardiac glycogenosis (disorder)

Shortest Term

Cardiac glycogenosis

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Cardiac glycogenosis (disorder)

SCTID: 195025008, Defined, Active

195025008|Cardiac glycogenosis (disorder)|

en Cardiac glycogenosis
en Cardiac glycogenosis (disorder)

Expression

195025008 |Cardiac glycogenosis (disorder)|
 === 363005004 |Cardiovascular system hereditary disorder (disorder)| + 
29633007 |Glycogen storage disease (disorder)| + 
871646007 |Infiltrative cardiomyopathy (disorder)| + 
762228008 |Congenital cardiovascular disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 23521003 |Glycogen deposition (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 74281007 |Myocardium structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
300044016 - Cardiac glycogenosis (en) View
300044016	en	Synonym (core metadata concept)	Cardiac glycogenosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
579073010 - Cardiac glycogenosis (disorder) (en) View
579073010	en	Fully specified name (core metadata concept)	Cardiac glycogenosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13799211025) - 195025008 -> 64077000 (116680003) View
116680003 \|Is a (attribute)\|	64077000 \|Myocardial degeneration (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13884257025) - 195025008 -> 871646007 (116680003) View
116680003 \|Is a (attribute)\|	871646007 \|Infiltrative cardiomyopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (327257022) - 195025008 -> 195023001 (116680003) View
116680003 \|Is a (attribute)\|	195023001 \|Nutritional and metabolic cardiomyopathies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13797634024) - 195025008 -> 762228008 (116680003) View
116680003 \|Is a (attribute)\|	762228008 \|Congenital cardiovascular disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13797635020) - 195025008 -> 29633007 (116680003) View
116680003 \|Is a (attribute)\|	29633007 \|Glycogen storage disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13797636021) - 195025008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13797638022) - 195025008 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13797649027) - 195025008 -> 23521003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23521003 \|Glycogen deposition (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (961748029) - 195025008 -> 74281007 (363698007) View
363698007 \|Finding site (attribute)\|	74281007 \|Myocardium structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
871646007 View
871646007	Infiltrative cardiomyopathy (disorder)	Infiltrative cardiomyopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
762228008 View
762228008	Congenital cardiovascular disorder (disorder)	Congenital cardiovascular disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
29633007 View
29633007	Glycogen storage disease (disorder)	Glycogenosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363005004 View
363005004	Cardiovascular system hereditary disorder (disorder)	Cardiovascular system hereditary disorder	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 (795fcc83-3137-5d8b-81d1-641418b2af6f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I43.1	TRUE	ALWAYS I43.1 \| THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE	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 (c32cd225-1cb0-5937-8b38-a2af0baffc85) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E74.0	TRUE	ALWAYS E74.0	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)\|

Terminology chevron_right Concepts chevron_right 195025008

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