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Terminology chevron_right Concepts chevron_right 22011005

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Component

22011005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hartnup disorder, renal type (disorder)

Shortest Term

Hartnup disorder, renal 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 type (disorder)

SCTID: 22011005, Primitive, Active

22011005|Hartnup disorder, renal type (disorder)|

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

Expression

22011005 |Hartnup disorder, renal type (disorder)|
 <<< 80902009 |Neutral 1 amino acid transport defect (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
751372013 - Hartnup disorder, renal type (disorder) (en) View
751372013	en	Fully specified name (core metadata concept)	Hartnup disorder, renal type (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
36922015 - Hartnup disorder, renal type (en) View
36922015	en	Synonym (core metadata concept)	Hartnup disorder, renal type	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (727237026) - 22011005 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (727238020) - 22011005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (183959021) - 22011005 -> 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
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 (4622234d-0fad-5210-97e5-ae8f514be27b) 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)\|

Terminology chevron_right Concepts chevron_right 22011005

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