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Terminology chevron_right Concepts chevron_right 447292006

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Component

447292006

The component that hold information about this concept.

Fully Specified Name (FSN)

Mitochondrial encephalomyopathy (disorder)

Shortest Term

Mitochondrial encephalomyopathy

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

Mitochondrial encephalomyopathy (disorder)

SCTID: 447292006, Primitive, Active

447292006|Mitochondrial encephalomyopathy (disorder)|

en Mitochondrial encephalomyopathy
en Mitochondrial encephalomyopathy (disorder)
en Mitochondrial myoencephalopathy

Expression

447292006 |Mitochondrial encephalomyopathy (disorder)|
 <<< 81308009 |Disorder of brain (disorder)| + 
16851005 |Mitochondrial myopathy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2883571014 - Mitochondrial encephalomyopathy (en) View
2883571014	en	Synonym (core metadata concept)	Mitochondrial encephalomyopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2880725016 - Mitochondrial encephalomyopathy (disorder) (en) View
2880725016	en	Fully specified name (core metadata concept)	Mitochondrial encephalomyopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2883572019 - Mitochondrial myoencephalopathy (en) View
2883572019	en	Synonym (core metadata concept)	Mitochondrial myoencephalopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3799786024) - 447292006 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3799787026) - 447292006 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3795200023) - 447292006 -> 280128006 (116680003) View
116680003 \|Is a (attribute)\|	280128006 \|Disorder of soft tissue of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3795201022) - 447292006 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3795202026) - 447292006 -> 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
16851005 View
16851005	Mitochondrial myopathy (disorder)	Ragged red myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
81308009 View
81308009	Disorder of brain (disorder)	Encephalopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1186718008 View
1186718008	Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome (disorder)	Coq4-related neonatal encephalomyopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
778029000 View
778029000	Fast kinase domains 2-related infantile mitochondrial encephalomyopathy (disorder)	Fastkd2-related infantile mitochondrial encephalomyopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
763688008 View
763688008	Deafness, encephaloneuropathy, obesity, valvulopathy syndrome (disorder)	Deafness, encephaloneuropathy, obesity, valvulopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
765401006 View
765401006	Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder)	Mitochondrial dna depletion syndrome encephalomyopathic form	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722212004 View
722212004	Severe x-linked mitochondrial encephalomyopathy (disorder)	Severe x-linked mitochondrial encephalomyopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
718214007 View
718214007	Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)	Mitochondrial neurogastrointestinal encephalomyopathy syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230426003 View
230426003	Myoclonic epilepsy - ragged red fibers (disorder)	Fukuhara syndrome	900000000000074008 \|Necessary but not sufficient concept 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 (baab2f31-c7ad-59e5-8b04-09de35b90a2a) 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)\|

Terminology chevron_right Concepts chevron_right 447292006

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