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Terminology chevron_right Concepts chevron_right 236526008

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Renal disorders in inherited disease (disorder)

Shortest Term

Renal disorders in inherited disease

Definition Status

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

Summary

Renal disorders in inherited disease (disorder)

SCTID: 236526008, Primitive, Inactive

236526008|Renal disorders in inherited disease (disorder)|

Expression

236526008 |Renal disorders in inherited disease (disorder)|
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Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
354545012 - Renal disorders in inherited disease (en) View
354545012	en	Synonym (core metadata concept)	Renal disorders in inherited disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
625132016 - Renal disorders in inherited disease (disorder) (en) View
625132016	en	Fully specified name (core metadata concept)	Renal disorders in inherited disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (51612026) - 236526008 -> 90708001 (116680003) View
116680003 \|Is a (attribute)\|	90708001 \|Kidney disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (522756026) - 236526008 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

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 (f96e6555-d9c6-52e8-9705-3fc59c5787af) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N28.9	TRUE	ALWAYS N28.9	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)\|

Descriptions