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Terminology chevron_right Concepts chevron_right 81987005

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Component

81987005

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial hypokalemic alkalosis, gullner type (disorder)

Shortest Term

Gullner syndrome

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 alkalosis, gullner type (disorder)

SCTID: 81987005, Primitive, Active

81987005|Familial hypokalemic alkalosis, gullner type (disorder)|

vi Nhiễm kiềm hạ kali máu gia đình, typ gullner
en Familial hypokalaemia
en Familial hypokalemia
en Gullner's syndrome
en Familial hypokalaemic alkalosis, gullner type
en Familial hypokalemic alkalosis, gullner type
en Familial hypokalemic alkalosis, gullner type (disorder)
en Gullner syndrome

Expression

81987005 |Familial hypokalemic alkalosis, gullner type (disorder)|
 <<< 22774003 |Hypokalemic alkalosis (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
111941005 |Familial disease (disorder)| + 
236470002 |Specific renal tubule transport defect (disorder)| + 
106000008 |Metabolic renal disease (disorder)| + 
367591000119105 |Hereditary nephropathy (disorder)| : 
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3401000269110 - nhiễm kiềm hạ kali máu gia đình, typ Gullner (vi) View
3401000269110	vi	Synonym (core metadata concept)	nhiễm kiềm hạ kali máu gia đình, typ Gullner	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
504851014 - Familial hypokalaemia (en) View
504851014	en	Synonym (core metadata concept)	Familial hypokalaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
135995015 - Familial hypokalemia (en) View
135995015	en	Synonym (core metadata concept)	Familial hypokalemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1234669018 - Gullner's syndrome (en) View
1234669018	en	Synonym (core metadata concept)	Gullner's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
504852019 - Familial hypokalaemic alkalosis, Gullner type (en) View
504852019	en	Synonym (core metadata concept)	Familial hypokalaemic alkalosis, Gullner type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
135994016 - Familial hypokalemic alkalosis, Gullner type (en) View
135994016	en	Synonym (core metadata concept)	Familial hypokalemic alkalosis, Gullner type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
823318013 - Familial hypokalemic alkalosis, Gullner type (disorder) (en) View
823318013	en	Fully specified name (core metadata concept)	Familial hypokalemic alkalosis, Gullner type (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
135996019 - Gullner syndrome (en) View
135996019	en	Synonym (core metadata concept)	Gullner syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15058008027) - 81987005 -> 106000008 (116680003) View
116680003 \|Is a (attribute)\|	106000008 \|Metabolic renal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (878890021) - 81987005 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (281229028) - 81987005 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5981569027) - 81987005 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (281228020) - 81987005 -> 236470002 (116680003) View
116680003 \|Is a (attribute)\|	236470002 \|Specific renal tubule transport defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (281230022) - 81987005 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (281231021) - 81987005 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (281232025) - 81987005 -> 22774003 (116680003) View
116680003 \|Is a (attribute)\|	22774003 \|Hypokalemic alkalosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
106000008 View
106000008	Metabolic renal disease (disorder)	Metabolic renal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
367591000119105 View
367591000119105	Hereditary nephropathy (disorder)	Hereditary nephropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
22774003 View
22774003	Hypokalemic alkalosis (disorder)	Hypokalemic alkalosis	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
111941005 View
111941005	Familial disease (disorder)	Familial disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236470002 View
236470002	Specific renal tubule transport defect (disorder)	Specific renal tubule transport defect	900000000000074008 \|Necessary but not sufficient concept 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 (28c8c1b6-27fb-5eaa-a10a-bd2ad5cf5ec8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E87.8	TRUE	ALWAYS E87.8	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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