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Terminology chevron_right Concepts chevron_right 237651005

Production

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Component

237651005

The component that hold information about this concept.

Fully Specified Name (FSN)

Insulin resistance - type a (disorder)

Shortest Term

Type a insulin resistance

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

Insulin resistance - type a (disorder)

SCTID: 237651005, Primitive, Active

237651005|Insulin resistance - type a (disorder)|

en Type a insulin resistance
en Insulin resistance - type a
en Insulin resistance - type a (disorder)

Expression

237651005 |Insulin resistance - type a (disorder)|
 <<< 609569007 |Diabetes mellitus due to genetic defect in insulin action (disorder)| + 
1899006 |Autosomal hereditary disorder (disorder)| + 
763325000 |Insulin resistance (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| : 
        { 363698007 |Finding site (attribute)| = 113331007 |Structure of endocrine system (body structure)| }
        { 42752001 |Due to (attribute)| = 782964007 |Genetic disease (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2475901019 - Type A insulin resistance (en) View
2475901019	en	Synonym (core metadata concept)	Type A insulin resistance	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
356181016 - Insulin resistance - type A (en) View
356181016	en	Synonym (core metadata concept)	Insulin resistance - type A	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
626410010 - Insulin resistance - type A (disorder) (en) View
626410010	en	Fully specified name (core metadata concept)	Insulin resistance - type A (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16409697024) - 237651005 -> 782964007 (42752001) View
42752001 \|Due to (attribute)\|	782964007 \|Genetic disease (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9107613020) - 237651005 -> 363137000 (116680003) View
116680003 \|Is a (attribute)\|	363137000 \|Hereditary disorder by system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12876689020) - 237651005 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4731854025) - 237651005 -> 113331007 (363698007) View
363698007 \|Finding site (attribute)\|	113331007 \|Structure of endocrine system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (53215029) - 237651005 -> 48606007 (116680003) View
116680003 \|Is a (attribute)\|	48606007 \|Drug resistance to insulin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3659434024) - 237651005 -> 410942007 (47429007) View
47429007 \|Associated with (attribute)\|	410942007 \|Drug or medicament (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9107612026) - 237651005 -> 1899006 (116680003) View
116680003 \|Is a (attribute)\|	1899006 \|Autosomal hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9107614025) - 237651005 -> 763325000 (116680003) View
116680003 \|Is a (attribute)\|	763325000 \|Insulin resistance (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4733397020) - 237651005 -> 609569007 (116680003) View
116680003 \|Is a (attribute)\|	609569007 \|Diabetes mellitus due to genetic defect in insulin action (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2853940028) - 237651005 -> 410942007 (246075003) View
246075003 \|Causative agent (attribute)\|	410942007 \|Drug or medicament (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1729704026) - 237651005 -> 113331007 (363698007) View
363698007 \|Finding site (attribute)\|	113331007 \|Structure of endocrine system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1729703021) - 237651005 -> 373873005 (246075003) View
246075003 \|Causative agent (attribute)\|	373873005 \|Pharmaceutical / biologic product (product)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2575184027) - 237651005 -> 410942007 (246075003) View
246075003 \|Causative agent (attribute)\|	410942007 \|Drug or medicament (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2476982026) - 237651005 -> 311980000 (246075003) View
246075003 \|Causative agent (attribute)\|	311980000 \|Drug, medicament or biological substance (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526302022) - 237651005 -> 2533004 (246075003) View
246075003 \|Causative agent (attribute)\|	2533004 \|Drug (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526303028) - 237651005 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
763325000 View
763325000	Insulin resistance (disorder)	Insulin resistance	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
609569007 View
609569007	Diabetes mellitus due to genetic defect in insulin action (disorder)	Diabetes mellitus due to genetic defect in insulin action	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1899006 View
1899006	Autosomal hereditary disorder (disorder)	Autosomal hereditary disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (32fd37e6-07b6-5c5f-a059-0ac4cb454011) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E13.6	TRUE	ALWAYS E13.6	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 (6bd5cedc-44c5-5c41-88d7-ab8ead9fbb85) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E13.9	TRUE	ALWAYS E13.9	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)\|

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