dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 267607008

Production

add

Component

267607008

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial periodic paralysis (disorder)

Shortest Term

Cavarre disease

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 periodic paralysis (disorder)

SCTID: 267607008, Primitive, Active

267607008|Familial periodic paralysis (disorder)|

en Familial myoplegia
en Familial periodic paralysis
en Familial periodic paralysis (disorder)
en Familial recurrent paralysis
en Myoplegic dystrophy
en Periodic myotonia
en Cavarre disease

Expression

267607008 |Familial periodic paralysis (disorder)|
 <<< 26111005 |Metabolic myopathy (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
399425011 - Familial myoplegia (en) View
399425011	en	Synonym (core metadata concept)	Familial myoplegia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
399422014 - Familial periodic paralysis (en) View
399422014	en	Synonym (core metadata concept)	Familial periodic paralysis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
660244012 - Familial periodic paralysis (disorder) (en) View
660244012	en	Fully specified name (core metadata concept)	Familial periodic paralysis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
399424010 - Familial recurrent paralysis (en) View
399424010	en	Synonym (core metadata concept)	Familial recurrent paralysis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
399423016 - Myoplegic dystrophy (en) View
399423016	en	Synonym (core metadata concept)	Myoplegic dystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
399428013 - Periodic myotonia (en) View
399428013	en	Synonym (core metadata concept)	Periodic myotonia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
399426012 - Westphal disease (en) View
399426012	en	Synonym (core metadata concept)	Westphal disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
399427015 - Cavarre disease (en) View
399427015	en	Synonym (core metadata concept)	Cavarre disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (594930024) - 267607008 -> 127954009 (363698007) View
363698007 \|Finding site (attribute)\|	127954009 \|Skeletal muscle structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (88967028) - 267607008 -> 26111005 (116680003) View
116680003 \|Is a (attribute)\|	26111005 \|Metabolic myopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
26111005 View
26111005	Metabolic myopathy (disorder)	Metabolic myopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
30967002 View
30967002	Thyrotoxic periodic paralysis (disorder)	Hashitoxic periodic paralysis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
40381009 View
40381009	Familial normokalemic periodic paralysis (disorder)	Periodic paralysis iii	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
82732003 View
82732003	Familial hypokalemic periodic paralysis (disorder)	Periodic paralysis i	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
304737009 View
304737009	Familial hyperkalemic periodic paralysis (disorder)	Gamstorp disease	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 (c8b3c8f3-d240-55d1-b4a5-eeb137ca6a6d) 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)\|

Terminology chevron_right Concepts chevron_right 267607008

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches