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Terminology chevron_right Concepts chevron_right 230676009

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Component

230676009

The component that hold information about this concept.

Fully Specified Name (FSN)

Putative defect in acetylcholine synthesis or packaging (disorder)

Shortest Term

Putative defect in acetylcholine synthesis or packaging

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

Putative defect in acetylcholine synthesis or packaging (disorder)

SCTID: 230676009, Primitive, Active

230676009|Putative defect in acetylcholine synthesis or packaging (disorder)|

en Putative defect in acetylcholine synthesis or packaging
en Putative defect in acetylcholine synthesis or packaging (disorder)

Expression

230676009 |Putative defect in acetylcholine synthesis or packaging (disorder)|
 <<< 230669004 |Genetically determined myasthenia (disorder)| : 
        { 363698007 |Finding site (attribute)| = 31627007 |Neuromuscular junction (cell structure)|,
370135005 |Pathological process (attribute)| = 263680009 |Autoimmune process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 127954009 |Skeletal muscle structure (body structure)| }
        { 370135005 |Pathological process (attribute)| = 472963003 |Hypersensitivity process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
345615017 - Putative defect in acetylcholine synthesis or packaging (en) View
345615017	en	Synonym (core metadata concept)	Putative defect in acetylcholine synthesis or packaging	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
618516013 - Putative defect in acetylcholine synthesis or packaging (disorder) (en) View
618516013	en	Fully specified name (core metadata concept)	Putative defect in acetylcholine synthesis or packaging (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (492901022) - 230676009 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (492902026) - 230676009 -> 31627007 (363698007) View
363698007 \|Finding site (attribute)\|	31627007 \|Neuromuscular junction (cell structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1724586027) - 230676009 -> 263680009 (370135005) View
370135005 \|Pathological process (attribute)\|	263680009 \|Autoimmune process (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4675189025) - 230676009 -> 472963003 (370135005) View
370135005 \|Pathological process (attribute)\|	472963003 \|Hypersensitivity process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11530752029) - 230676009 -> 31627007 (363698007) View
363698007 \|Finding site (attribute)\|	31627007 \|Neuromuscular junction (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11530753023) - 230676009 -> 263680009 (370135005) View
370135005 \|Pathological process (attribute)\|	263680009 \|Autoimmune process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2710004025) - 230676009 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3777820023) - 230676009 -> 421961002 (42752001) View
42752001 \|Due to (attribute)\|	421961002 \|Hypersensitivity reaction (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3187296026) - 230676009 -> 418925002 (42752001) View
42752001 \|Due to (attribute)\|	418925002 \|Immune hypersensitivity reaction (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (492900023) - 230676009 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (41227027) - 230676009 -> 230669004 (116680003) View
116680003 \|Is a (attribute)\|	230669004 \|Genetically determined myasthenia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
230669004 View
230669004	Genetically determined myasthenia (disorder)	Genetically determined myasthenia	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 (dadebac6-6e9c-5b77-91bc-b2b8a8750347) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G70.0	TRUE	ALWAYS G70.0 \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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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