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Terminology chevron_right Concepts chevron_right 444645005

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Component

444645005

The component that hold information about this concept.

Fully Specified Name (FSN)

Dent's disease (disorder)

Shortest Term

Dent 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

Dent's disease (disorder)

SCTID: 444645005, Primitive, Active

444645005|Dent's disease (disorder)|

en Dent disease
en Dent's disease
en Dent's disease (disorder)

Expression

444645005 |Dent's disease (disorder)|
 <<< 367591000119105 |Hereditary nephropathy (disorder)| + 
1162976004 |X-linked recessive hereditary disease (disorder)| + 
95568003 |Renal tubular disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 50468005 |Proximal convoluted renal tubule structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2871629019 - Dent disease (en) View
2871629019	en	Synonym (core metadata concept)	Dent disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2871630012 - Dent's disease (en) View
2871630012	en	Synonym (core metadata concept)	Dent's disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
2869211018 - Dent's disease (disorder) (en) View
2869211018	en	Fully specified name (core metadata concept)	Dent's disease (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3773082025) - 444645005 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3778135020) - 444645005 -> 64033007 (363698007) View
363698007 \|Finding site (attribute)\|	64033007 \|Kidney structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14008417024) - 444645005 -> 1162976004 (116680003) View
116680003 \|Is a (attribute)\|	1162976004 \|X-linked recessive hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008418025) - 444645005 -> 95568003 (116680003) View
116680003 \|Is a (attribute)\|	95568003 \|Renal tubular disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14008419022) - 444645005 -> 50468005 (363698007) View
363698007 \|Finding site (attribute)\|	50468005 \|Proximal convoluted renal tubule structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3773081021) - 444645005 -> 236526008 (116680003) View
116680003 \|Is a (attribute)\|	236526008 \|Renal disorders in inherited disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3773080022) - 444645005 -> 363338001 (116680003) View
116680003 \|Is a (attribute)\|	363338001 \|Hereditary disorder of the urinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5971859022) - 444645005 -> 367591000119105 (116680003) View
116680003 \|Is a (attribute)\|	367591000119105 \|Hereditary nephropathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1162976004 View
1162976004	X-linked recessive hereditary disease (disorder)	X-linked recessive hereditary disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
367591000119105 View
367591000119105	Hereditary nephropathy (disorder)	Hereditary nephropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95568003 View
95568003	Renal tubular disorder (disorder)	Rối loạn ống thận	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
717789008 View
717789008	Dent disease type 1 (disorder)	Dent disease type 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717790004 View
717790004	Dent disease type 2 (disorder)	Dent disease type 2	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
236713006 View
236713006	X-linked recessive nephrolithiasis with renal failure (disorder)	X-linked recessive nephrolithiasis with renal failure	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 (94992154-b378-5816-bc9b-957e938d74a6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N25.8	TRUE	ALWAYS N25.8	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)\|
ExtendedMap object (aa0c072e-7ff8-5f16-a2ea-1b2c47dea428) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.2	TRUE	ALWAYS Q78.2	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 444645005

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