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Terminology chevron_right Concepts chevron_right 80902009

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Component

80902009

The component that hold information about this concept.

Fully Specified Name (FSN)

Neutral 1 amino acid transport defect (disorder)

Shortest Term

Hartnup disease

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

Neutral 1 amino acid transport defect (disorder)

SCTID: 80902009, Primitive, Active

80902009|Neutral 1 amino acid transport defect (disorder)|

vi Khiếm khuyết vận chuyển acid amin 1 trung tính
en Neutral 1 amino acid transport defect
en Neutral 1 amino acid transport defect (disorder)
en Neutral amino acid transport defect
en Hartnup disease
en Hartnup disorder

Expression

80902009 |Neutral 1 amino acid transport defect (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
3611000269110 - khiếm khuyết vận chuyển acid amin 1 trung tính (vi) View
3611000269110	vi	Synonym (core metadata concept)	khiếm khuyết vận chuyển acid amin 1 trung tính	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
134190018 - Neutral 1 amino acid transport defect (en) View
134190018	en	Synonym (core metadata concept)	Neutral 1 amino acid transport defect	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
822114012 - Neutral 1 amino acid transport defect (disorder) (en) View
822114012	en	Fully specified name (core metadata concept)	Neutral 1 amino acid transport defect (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1234522018 - Neutral amino acid transport defect (en) View
1234522018	en	Synonym (core metadata concept)	Neutral amino acid transport defect	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
134191019 - Hartnup disease (en) View
134191019	en	Synonym (core metadata concept)	Hartnup disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
134192014 - Hartnup disorder (en) View
134192014	en	Synonym (core metadata concept)	Hartnup disorder	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15058005029) - 80902009 -> 106000008 (116680003) View
116680003 \|Is a (attribute)\|	106000008 \|Metabolic renal disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (876011027) - 80902009 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (279512022) - 80902009 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (876010026) - 80902009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (279510025) - 80902009 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (279511026) - 80902009 -> 236470002 (116680003) View
116680003 \|Is a (attribute)\|	236470002 \|Specific renal tubule transport defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (279513028) - 80902009 -> 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
22011005 View
22011005	Hartnup disorder, renal type (disorder)	Hartnup disorder, renal type	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
36891003 View
36891003	Hartnup disorder, renal/jejunal type (disorder)	Hartnup disorder, renal/jejunal type	900000000000074008 \|Necessary but not sufficient concept 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 (3fed4d6f-77e3-539a-b252-e1a1a3706306) 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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