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Terminology chevron_right Concepts chevron_right 1187635008

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Component

1187635008

The component that hold information about this concept.

Fully Specified Name (FSN)

Maternally inherited mitochondrial cardiomyopathy (disorder)

Shortest Term

Maternally inherited mitochondrial cardiomyopathy

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

Maternally inherited mitochondrial cardiomyopathy (disorder)

SCTID: 1187635008, Defined, Active

1187635008|Maternally inherited mitochondrial cardiomyopathy (disorder)|

en Maternally inherited mitochondrial cardiomyopathy
en Maternally inherited mitochondrial cardiomyopathy (disorder)

Expression

1187635008 |Maternally inherited mitochondrial cardiomyopathy (disorder)|
 === 1162975000 |Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)| + 
363005004 |Cardiovascular system hereditary disorder (disorder)| + 
472315005 |Mitochondrial cardiomyopathy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 74281007 |Myocardium structure (body structure)| }
        { 42752001 |Due to (attribute)| = 240096000 |Mitochondrial cytopathy (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4674560017 - Maternally inherited mitochondrial cardiomyopathy (en) View
4674560017	en	Synonym (core metadata concept)	Maternally inherited mitochondrial cardiomyopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4674559010 - Maternally inherited mitochondrial cardiomyopathy (disorder) (en) View
4674559010	en	Fully specified name (core metadata concept)	Maternally inherited mitochondrial cardiomyopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14976811023) - 1187635008 -> 16851005 (116680003) View
116680003 \|Is a (attribute)\|	16851005 \|Mitochondrial myopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14976813021) - 1187635008 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14976814026) - 1187635008 -> 40172005 (116680003) View
116680003 \|Is a (attribute)\|	40172005 \|Cardiac complication (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14976815025) - 1187635008 -> 57809008 (116680003) View
116680003 \|Is a (attribute)\|	57809008 \|Myocardial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14976818028) - 1187635008 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15778777022) - 1187635008 -> 60738003 (116680003) View
116680003 \|Is a (attribute)\|	60738003 \|Secondary myopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15852492028) - 1187635008 -> 472315005 (116680003) View
116680003 \|Is a (attribute)\|	472315005 \|Mitochondrial cardiomyopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14976810024) - 1187635008 -> 1162975000 (116680003) View
116680003 \|Is a (attribute)\|	1162975000 \|Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14976812027) - 1187635008 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14976816029) - 1187635008 -> 240096000 (42752001) View
42752001 \|Due to (attribute)\|	240096000 \|Mitochondrial cytopathy (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14976817022) - 1187635008 -> 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
1162975000 View
1162975000	Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)	Maternally inherited mitochondrial disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
472315005 View
472315005	Mitochondrial cardiomyopathy (disorder)	Mitochondrial cardiomyopathy	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
472320005 View
472320005	Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder)	Maternally inherited mitochondrial cardiomyopathy and myopathy	900000000000073002 \|Sufficiently defined by necessary conditions 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 (2f9965a0-e12c-5dbe-b56c-17bd81e3effd) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.8	TRUE	ALWAYS E88.8	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)\|
ExtendedMap object (88cbbb00-c112-51de-838f-2b5d92693419) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G71.3	TRUE	ALWAYS G71.3	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 (9c73a905-90b7-55cb-8b8b-23505ed42a72) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I42.9	TRUE	ALWAYS I42.9	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 (cd1c8836-13ea-5a9b-a283-003ee98ce1d8) 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)\|

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