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Terminology chevron_right Concepts chevron_right 768553002

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Component

768553002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hypermanganesemia with dystonia (disorder)

Shortest Term

Hypermanganesemia with dystonia

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

Hypermanganesemia with dystonia (disorder)

SCTID: 768553002, Primitive, Active

768553002|Hypermanganesemia with dystonia (disorder)|

en Familial manganese-induced neurotoxicity
en Hmndyt - hypermanganesemia with dystonia
en Hypermanganesemia with dystonia
en Hypermanganesemia with dystonia (disorder)

Expression

768553002 |Hypermanganesemia with dystonia (disorder)|
 <<< 363235000 |Hereditary disorder of nervous system (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
63656007 |Disorder of manganese metabolism (disorder)| + 
15802004 |Dystonia (disorder)| : 
        { 363698007 |Finding site (attribute)| = 76375004 |Extrapyramidal system structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3686023014 - Familial manganese-induced neurotoxicity (en) View
3686023014	en	Synonym (core metadata concept)	Familial manganese-induced neurotoxicity	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3686024015 - HMNDYT - hypermanganesemia with dystonia (en) View
3686024015	en	Synonym (core metadata concept)	HMNDYT - hypermanganesemia with dystonia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3686022016 - Hypermanganesemia with dystonia (en) View
3686022016	en	Synonym (core metadata concept)	Hypermanganesemia with dystonia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3686021011 - Hypermanganesemia with dystonia (disorder) (en) View
3686021011	en	Fully specified name (core metadata concept)	Hypermanganesemia with dystonia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13882858025) - 768553002 -> 255324009 (363714003) View
363714003 \|Interprets (attribute)\|	255324009 \|Movement (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16350686023) - 768553002 -> 363847004 (363714003) View
363714003 \|Interprets (attribute)\|	363847004 \|Movement observable (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9443066022) - 768553002 -> 76375004 (363698007) View
363698007 \|Finding site (attribute)\|	76375004 \|Extrapyramidal system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9443063025) - 768553002 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9443064020) - 768553002 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9443065021) - 768553002 -> 63656007 (116680003) View
116680003 \|Is a (attribute)\|	63656007 \|Disorder of manganese metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9443067029) - 768553002 -> 15802004 (116680003) View
116680003 \|Is a (attribute)\|	15802004 \|Dystonia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
15802004 View
15802004	Dystonia (disorder)	Dystonia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63656007 View
63656007	Disorder of manganese metabolism (disorder)	Disorder of manganese metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
768554008 View
768554008	Hypermanganesemia with dystonia 2 (disorder)	Hypermanganesemia with dystonia 2	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
702377007 View
702377007	Hypermanganesemia with dystonia, polycythemia, and cirrhosis (disorder)	Hypermanganesemia with dystonia, polycythemia, and cirrhosis	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 (4dead5aa-1299-5703-82ea-93fa8b7dedbb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G24.9	TRUE	ALWAYS G24.9	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 (e8c13152-46f7-5906-954f-18e5c6586d52) 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 (f03d12b4-b18e-5f21-8fe7-fccd891251fe) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.8	TRUE	ALWAYS E83.8	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)\|

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