dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 707756004

Production

add

Component

707756004

The component that hold information about this concept.

Fully Specified Name (FSN)

Gitelman syndrome (disorder)

Shortest Term

Gitelman 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

Gitelman syndrome (disorder)

SCTID: 707756004, Primitive, Active

707756004|Gitelman syndrome (disorder)|

en Gitelman's syndrome
en Gitelman syndrome
en Gitelman syndrome (disorder)

Expression

707756004 |Gitelman syndrome (disorder)|
 <<< 80710001 |Primary hypomagnesemia (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
22774003 |Hypokalemic alkalosis (disorder)| + 
54879000 |Hypokalemic nephropathy (disorder)| + 
735475005 |Renal hypocalciuria (disorder)| + 
363045008 |Connective tissue hereditary disorder (disorder)| + 
367591000119105 |Hereditary nephropathy (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 409774005 |Inflammatory morphology (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 50235001 |Structure of interstitial tissue of kidney (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 409774005 |Inflammatory morphology (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 58471003 |Renal tubule structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3031308017 - Gitelman's syndrome (en) View
3031308017	en	Synonym (core metadata concept)	Gitelman's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3031375018 - Gitelman syndrome (en) View
3031375018	en	Synonym (core metadata concept)	Gitelman syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3031384018 - Gitelman syndrome (disorder) (en) View
3031384018	en	Fully specified name (core metadata concept)	Gitelman syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5987507023) - 707756004 -> 707755000 (116680003) View
116680003 \|Is a (attribute)\|	707755000 \|Familial hypokalemic and hypomagnesemic tubulopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15870715023) - 707756004 -> 22774003 (116680003) View
116680003 \|Is a (attribute)\|	22774003 \|Hypokalemic alkalosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15870716024) - 707756004 -> 54879000 (116680003) View
116680003 \|Is a (attribute)\|	54879000 \|Hypokalemic nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15870717026) - 707756004 -> 80710001 (116680003) View
116680003 \|Is a (attribute)\|	80710001 \|Primary hypomagnesemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15097301024) - 707756004 -> 363045008 (116680003) View
116680003 \|Is a (attribute)\|	363045008 \|Connective tissue hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15097302028) - 707756004 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15097303022) - 707756004 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5987508029) - 707756004 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5987509021) - 707756004 -> 29704000 (363698007) View
363698007 \|Finding site (attribute)\|	29704000 \|Structure of parenchyma of kidney (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5987510027) - 707756004 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5987511028) - 707756004 -> 50235001 (363698007) View
363698007 \|Finding site (attribute)\|	50235001 \|Structure of interstitial tissue of kidney (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12088489020) - 707756004 -> 409774005 (116676008) View
116676008 \|Associated morphology (attribute)\|	409774005 \|Inflammatory morphology (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088490027) - 707756004 -> 409774005 (116676008) View
116676008 \|Associated morphology (attribute)\|	409774005 \|Inflammatory morphology (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088491028) - 707756004 -> 50235001 (363698007) View
363698007 \|Finding site (attribute)\|	50235001 \|Structure of interstitial tissue of kidney (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12088492024) - 707756004 -> 58471003 (363698007) View
363698007 \|Finding site (attribute)\|	58471003 \|Renal tubule structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5987506025) - 707756004 -> 86353007 (116680003) View
116680003 \|Is a (attribute)\|	86353007 \|Hypocalciuria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7216727023) - 707756004 -> 735475005 (116680003) View
116680003 \|Is a (attribute)\|	735475005 \|Renal hypocalciuria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
735475005 View
735475005	Renal hypocalciuria (disorder)	Renal hypocalciuria	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
363045008 View
363045008	Connective tissue hereditary disorder (disorder)	Connective tissue hereditary disorder	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
54879000 View
54879000	Hypokalemic nephropathy (disorder)	Osmotic nephrosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
80710001 View
80710001	Primary hypomagnesemia (disorder)	Primary hypomagnesemia	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

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 (b3eac91f-0202-5717-9c07-49bfcf56ef8d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N15.8	TRUE	ALWAYS N15.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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 707756004

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches