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Terminology chevron_right Concepts chevron_right 75652008

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Component

75652008

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial renal iminoglycinuria (disorder)

Shortest Term

Familial renal iminoglycinuria

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Familial renal iminoglycinuria (disorder)

SCTID: 75652008, Defined, Active

75652008|Familial renal iminoglycinuria (disorder)|

vi Rối loạn tái hấp thu glycin và imino ở thận có tính gia đình
en Familial renal iminoglycinuria
en Familial renal iminoglycinuria (disorder)

Expression

75652008 |Familial renal iminoglycinuria (disorder)|
 === 367591000119105 |Hereditary nephropathy (disorder)| + 
84121007 |Iminoglycinuria (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
111941005 |Familial disease (disorder)| + 
86095007 |Inborn error of metabolism (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5681000269118 - rối loạn tái hấp thu glycin và imino ở thận có tính gia đình (vi) View
5681000269118	vi	Synonym (core metadata concept)	rối loạn tái hấp thu glycin và imino ở thận có tính gia đình	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
125653016 - Familial renal iminoglycinuria (en) View
125653016	en	Synonym (core metadata concept)	Familial renal iminoglycinuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
816286010 - Familial renal iminoglycinuria (disorder) (en) View
816286010	en	Fully specified name (core metadata concept)	Familial renal iminoglycinuria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (862786024) - 75652008 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (862787026) - 75652008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2696698021) - 75652008 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5981050026) - 75652008 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2696699029) - 75652008 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (271022024) - 75652008 -> 111941005 (116680003) View
116680003 \|Is a (attribute)\|	111941005 \|Familial disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (271023025) - 75652008 -> 84121007 (116680003) View
116680003 \|Is a (attribute)\|	84121007 \|Iminoglycinuria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (271024020) - 75652008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
367591000119105 View
367591000119105	Hereditary nephropathy (disorder)	Hereditary nephropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
84121007 View
84121007	Iminoglycinuria (disorder)	Iminoglycinuria	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
86095007 View
86095007	Inborn error of metabolism (disorder)	Inborn error of metabolism	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

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 (09838e68-b4af-5495-aa03-0dec5d39ff08) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.8	TRUE	ALWAYS E72.8	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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