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Terminology chevron_right Concepts chevron_right 36891003

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Component

36891003

The component that hold information about this concept.

Fully Specified Name (FSN)

Hartnup disorder, renal/jejunal type (disorder)

Shortest Term

Hartnup disorder, renal/jejunal type

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

Hartnup disorder, renal/jejunal type (disorder)

SCTID: 36891003, Primitive, Active

36891003|Hartnup disorder, renal/jejunal type (disorder)|

en Hartnup disorder, renal/jejunal type (disorder)
en Hartnup disorder, renal/jejunal type

Expression

36891003 |Hartnup disorder, renal/jejunal type (disorder)|
 <<< 80902009 |Neutral 1 amino acid transport defect (disorder)| + 
304370001 |Disorder of jejunum (disorder)| : 
        { 363698007 |Finding site (attribute)| = 21306003 |Jejunal structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 64033007 |Kidney structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
768695018 - Hartnup disorder, renal/jejunal type (disorder) (en) View
768695018	en	Fully specified name (core metadata concept)	Hartnup disorder, renal/jejunal type (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
61539016 - Hartnup disorder, renal/jejunal type (en) View
61539016	en	Synonym (core metadata concept)	Hartnup disorder, renal/jejunal type	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (763929028) - 36891003 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (763931021) - 36891003 -> 21306003 (363698007) View
363698007 \|Finding site (attribute)\|	21306003 \|Jejunal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (207959023) - 36891003 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (763930022) - 36891003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (207955028) - 36891003 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (207957020) - 36891003 -> 119522002 (116680003) View
116680003 \|Is a (attribute)\|	119522002 \|Disorder of small intestine (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (207958026) - 36891003 -> 79787007 (116680003) View
116680003 \|Is a (attribute)\|	79787007 \|Disorder of lower gastrointestinal tract (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1673866025) - 36891003 -> 304370001 (116680003) View
116680003 \|Is a (attribute)\|	304370001 \|Disorder of jejunum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (207956027) - 36891003 -> 80902009 (116680003) View
116680003 \|Is a (attribute)\|	80902009 \|Neutral 1 amino acid transport defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
304370001 View
304370001	Disorder of jejunum (disorder)	Disorder of jejunum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
80902009 View
80902009	Neutral 1 amino acid transport defect (disorder)	Hartnup 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 (3cb8d94f-81af-59cb-8710-6279521eb0ef) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.0	TRUE	ALWAYS E72.0	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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