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Terminology chevron_right Concepts chevron_right 84121007

Production

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Component

84121007

The component that hold information about this concept.

Fully Specified Name (FSN)

Iminoglycinuria (disorder)

Shortest Term

Iminoglycinuria

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

Iminoglycinuria (disorder)

SCTID: 84121007, Primitive, Active

84121007|Iminoglycinuria (disorder)|

vi Iminoglycin niệu
en Iminoglycinuria
en Iminoglycinuria (disorder)

Expression

84121007 |Iminoglycinuria (disorder)|
 <<< 236470002 |Specific renal tubule transport defect (disorder)| + 
16784003 |Amino acid transport disorder (disorder)| + 
106000008 |Metabolic renal disease (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
2921000269115 - iminoglycin niệu (vi) View
2921000269115	vi	Synonym (core metadata concept)	iminoglycin niệu	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
139496018 - Iminoglycinuria (en) View
139496018	en	Synonym (core metadata concept)	Iminoglycinuria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
825899010 - Iminoglycinuria (disorder) (en) View
825899010	en	Fully specified name (core metadata concept)	Iminoglycinuria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
139497010 - Iminoglycinuria, NOS (en) View
139497010	en	Synonym (core metadata concept)	Iminoglycinuria, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15058010025) - 84121007 -> 106000008 (116680003) View
116680003 \|Is a (attribute)\|	106000008 \|Metabolic renal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (884403022) - 84121007 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (285011020) - 84121007 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (884402028) - 84121007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (285008024) - 84121007 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (285009027) - 84121007 -> 236470002 (116680003) View
116680003 \|Is a (attribute)\|	236470002 \|Specific renal tubule transport defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (285010021) - 84121007 -> 16784003 (116680003) View
116680003 \|Is a (attribute)\|	16784003 \|Amino acid transport disorder (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
16784003 View
16784003	Amino acid transport disorder (disorder)	Amino acid transport disorder	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
25765006 View
25765006	Neonatal iminoglycinuria (disorder)	Neonatal iminoglycinuria	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
75652008 View
75652008	Familial renal iminoglycinuria (disorder)	Familial renal iminoglycinuria	900000000000073002 \|Sufficiently defined by necessary conditions 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 (a5bb3464-a397-5f6b-a2a6-83f9f56366ff) 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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