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Terminology chevron_right Concepts chevron_right 82732003

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Component

82732003

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial hypokalemic periodic paralysis (disorder)

Shortest Term

Periodic paralysis i

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

Familial hypokalemic periodic paralysis (disorder)

SCTID: 82732003, Primitive, Active

82732003|Familial hypokalemic periodic paralysis (disorder)|

vi Liệt chu kỳ hạ kali huyết có tính chất gia đình
en Hokpp - hypokalaemic periodic paralysis
en Hokpp - hypokalemic periodic paralysis
en Familial hypokalaemic periodic paralysis
en Familial hypokalemic periodic paralysis
en Familial hypokalemic periodic paralysis (disorder)
en Hypokalaemic periodic paralysis
en Hypokalemic periodic paralysis
en Periodic paralysis i

Expression

82732003 |Familial hypokalemic periodic paralysis (disorder)|
 <<< 267607008 |Familial periodic paralysis (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363212003 |Hereditary disorder of musculoskeletal system (disorder)| : 
        { 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
510611000003110 - liệt chu kỳ hạ kali huyết có tính chất gia đình (vi) View
510611000003110	vi	Synonym (core metadata concept)	liệt chu kỳ hạ kali huyết có tính chất gia đình	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4572800012 - HOKPP - hypokalaemic periodic paralysis (en) View
4572800012	en	Synonym (core metadata concept)	HOKPP - hypokalaemic periodic paralysis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4572799013 - HOKPP - hypokalemic periodic paralysis (en) View
4572799013	en	Synonym (core metadata concept)	HOKPP - hypokalemic periodic paralysis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
505241013 - Familial hypokalaemic periodic paralysis (en) View
505241013	en	Synonym (core metadata concept)	Familial hypokalaemic periodic paralysis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
137245011 - Familial hypokalemic periodic paralysis (en) View
137245011	en	Synonym (core metadata concept)	Familial hypokalemic periodic paralysis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
824217011 - Familial hypokalemic periodic paralysis (disorder) (en) View
824217011	en	Fully specified name (core metadata concept)	Familial hypokalemic periodic paralysis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
137247015 - Hypokalaemic periodic paralysis (en) View
137247015	en	Synonym (core metadata concept)	Hypokalaemic periodic paralysis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
137246012 - Hypokalemic periodic paralysis (en) View
137246012	en	Synonym (core metadata concept)	Hypokalemic periodic paralysis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
505240014 - Periodic paralysis I (en) View
505240014	en	Synonym (core metadata concept)	Periodic paralysis I	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13805670023) - 82732003 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13805671022) - 82732003 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (881087029) - 82732003 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (282516025) - 82732003 -> 267607008 (116680003) View
116680003 \|Is a (attribute)\|	267607008 \|Familial periodic paralysis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
267607008 View
267607008	Familial periodic paralysis (disorder)	Cavarre disease	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 (15630f98-415c-5398-b434-b97ae680df56) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	G72.3	TRUE	ALWAYS G72.3	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)\|

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