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Terminology chevron_right Concepts chevron_right 472320005

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Component

472320005

The component that hold information about this concept.

Fully Specified Name (FSN)

Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder)

Shortest Term

Maternally inherited mitochondrial cardiomyopathy and myopathy

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 and myopathy (disorder)

SCTID: 472320005, Defined, Active

472320005|Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder)|

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

Expression

472320005 |Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder)|
 === 1187635008 |Maternally inherited mitochondrial cardiomyopathy (disorder)| + 
16851005 |Mitochondrial myopathy (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| + 
60738003 |Secondary myopathy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 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
2951114015 - Maternally inherited mitochondrial cardiomyopathy and myopathy (en) View
2951114015	en	Synonym (core metadata concept)	Maternally inherited mitochondrial cardiomyopathy and myopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2951122010 - Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder) (en) View
2951122010	en	Fully specified name (core metadata concept)	Maternally inherited mitochondrial cardiomyopathy and myopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4678121025) - 472320005 -> 472315005 (116680003) View
116680003 \|Is a (attribute)\|	472315005 \|Mitochondrial cardiomyopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12088715023) - 472320005 -> 363005004 (116680003) View
116680003 \|Is a (attribute)\|	363005004 \|Cardiovascular system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13902321021) - 472320005 -> 1162975000 (116680003) View
116680003 \|Is a (attribute)\|	1162975000 \|Maternally inherited mitochondrial deoxyribonucleic acid disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15851703025) - 472320005 -> 1187635008 (116680003) View
116680003 \|Is a (attribute)\|	1187635008 \|Maternally inherited mitochondrial cardiomyopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15778773021) - 472320005 -> 60738003 (116680003) View
116680003 \|Is a (attribute)\|	60738003 \|Secondary myopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088716024) - 472320005 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678122021) - 472320005 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678123027) - 472320005 -> 74281007 (363698007) View
363698007 \|Finding site (attribute)\|	74281007 \|Myocardium structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678124022) - 472320005 -> 240096000 (42752001) View
42752001 \|Due to (attribute)\|	240096000 \|Mitochondrial cytopathy (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4678120029) - 472320005 -> 16851005 (116680003) View
116680003 \|Is a (attribute)\|	16851005 \|Mitochondrial myopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1187635008 View
1187635008	Maternally inherited mitochondrial cardiomyopathy (disorder)	Maternally inherited mitochondrial cardiomyopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
16851005 View
16851005	Mitochondrial myopathy (disorder)	Ragged red myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
60738003 View
60738003	Secondary myopathy (disorder)	Secondary myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363212003 View
363212003	Hereditary disorder of musculoskeletal system (disorder)	Hereditary disorder of musculoskeletal 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 (0fb450dd-1988-55b5-94e0-1057540efee4) 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 (1c0cf6cf-2a8d-5409-9c8c-e2404a6c9f50) 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 (76980b07-97dd-51d7-943c-07c4b748f685) 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 (96e970dd-a308-5062-a8b2-aa88c72854b0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	I42.4	TRUE	ALWAYS I42.4	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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