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Terminology chevron_right Concepts chevron_right 237604008

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Component

237604008

The component that hold information about this concept.

Fully Specified Name (FSN)

Maturity onset diabetes of the young, type 2 (disorder)

Shortest Term

Mody2

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

Maturity onset diabetes of the young, type 2 (disorder)

SCTID: 237604008, Primitive, Active

237604008|Maturity onset diabetes of the young, type 2 (disorder)|

en Mody2 (maturity onset diabetes of the young type 2)
en Gck (glucokinase) monogenic diabetes mellitus
en Maturity onset diabetes in youth type 2
en Maturity onset diabetes of the young, type 2
en Maturity onset diabetes of the young, type 2 (disorder)
en Diabetes mellitus autosomal dominant type ii
en Maturity onset diabetes in youth type ii

Expression

237604008 |Maturity onset diabetes of the young, type 2 (disorder)|
 <<< 609561005 |Maturity-onset diabetes of the young (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (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
4635914013 - GCK monogenic diabetes mellitus (en) View
4635914013	en	Synonym (core metadata concept)	GCK monogenic diabetes mellitus	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
2967834013 - MODY2 (en) View
2967834013	en	Synonym (core metadata concept)	MODY2	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
5246522016 - MODY2 (maturity onset diabetes of the young type 2) (en) View
5246522016	en	Synonym (core metadata concept)	MODY2 (maturity onset diabetes of the young type 2)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
356087019 - MODY - Maturity onset diabetes glucokinase-related (en) View
356087019	en	Synonym (core metadata concept)	MODY - Maturity onset diabetes glucokinase-related	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
356086011 - MODY - Maturity onset diabetes in youth type 2 (en) View
356086011	en	Synonym (core metadata concept)	MODY - Maturity onset diabetes in youth type 2	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
356084014 - MODY - Maturity onset diabetes in youth type II (en) View
356084014	en	Synonym (core metadata concept)	MODY - Maturity onset diabetes in youth type II	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
4635913019 - GCK (glucokinase) monogenic diabetes mellitus (en) View
4635913019	en	Synonym (core metadata concept)	GCK (glucokinase) monogenic diabetes mellitus	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
356085010 - Maturity onset diabetes in youth type 2 (en) View
356085010	en	Synonym (core metadata concept)	Maturity onset diabetes in youth type 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2967875018 - Maturity onset diabetes of the young, type 2 (en) View
2967875018	en	Synonym (core metadata concept)	Maturity onset diabetes of the young, type 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2967841019 - Maturity onset diabetes of the young, type 2 (disorder) (en) View
2967841019	en	Fully specified name (core metadata concept)	Maturity onset diabetes of the young, type 2 (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626356015 - Diabetes mellitus autosomal dominant type II (disorder) (en) View
626356015	en	Fully specified name (core metadata concept)	Diabetes mellitus autosomal dominant type II (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
356082013 - Diabetes mellitus autosomal dominant type II (en) View
356082013	en	Synonym (core metadata concept)	Diabetes mellitus autosomal dominant type II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
356083015 - Maturity onset diabetes in youth type II (en) View
356083015	en	Synonym (core metadata concept)	Maturity onset diabetes in youth type II	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16418102021) - 237604008 -> 782964007 (42752001) View
42752001 \|Due to (attribute)\|	782964007 \|Genetic disease (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14018995028) - 237604008 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14018996027) - 237604008 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4598346026) - 237604008 -> 113331007 (363698007) View
363698007 \|Finding site (attribute)\|	113331007 \|Structure of endocrine system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (53141029) - 237604008 -> 28453007 (116680003) View
116680003 \|Is a (attribute)\|	28453007 \|Maturity onset diabetes mellitus in young (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2713106029) - 237604008 -> 290028006 (47429007) View
47429007 \|Associated with (attribute)\|	290028006 \|Genetic syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4733184028) - 237604008 -> 609561005 (116680003) View
116680003 \|Is a (attribute)\|	609561005 \|Maturity-onset diabetes of the young (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526221027) - 237604008 -> 78696007 (363698007) View
363698007 \|Finding site (attribute)\|	78696007 \|Endocrine pancreatic structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3351664028) - 237604008 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526222023) - 237604008 -> 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
609561005 View
609561005	Maturity-onset diabetes of the young (disorder)	Maturity-onset diabetes of the young	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	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 (2a53b400-4936-58b5-a257-38264cfbf98b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E11.9	TRUE	ALWAYS E11.9	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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