dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 721834007

Production

add

Component

721834007

The component that hold information about this concept.

Fully Specified Name (FSN)

Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)

Shortest Term

Hyperinsulinism due to ucp2 deficiency

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

Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)

SCTID: 721834007, Primitive, Active

721834007|Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)|

vi Tăng tiết insulin do thiếu hụt protein tách rời 2
en Hyperinsulinism due to uncoupling protein 2 deficiency
en Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)
en Hyperinsulinism due to ucp2 deficiency
en Hyperinsulinism due to ucp2 (uncoupling protein 2) deficiency

Expression

721834007 |Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
736652002 |Neonatal metabolic disorder (disorder)| + 
736653007 |Neonatal disorder of endocrine system (disorder)| + 
42357009 |Disorder of digestive system specific to fetus or newborn (disorder)| + 
1363361006 |Diazoxide-sensitive diffuse hyperinsulinism (disorder)| : 
        { 363698007 |Finding site (attribute)| = 78696007 |Endocrine pancreatic structure (body structure)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
455921000003118 - tăng tiết insulin do thiếu hụt protein tách rời 2 (vi) View
455921000003118	vi	Synonym (core metadata concept)	tăng tiết insulin do thiếu hụt protein tách rời 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
3326184017 - Hyperinsulinism due to uncoupling protein 2 deficiency (en) View
3326184017	en	Synonym (core metadata concept)	Hyperinsulinism due to uncoupling protein 2 deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3326183011 - Hyperinsulinism due to uncoupling protein 2 deficiency (disorder) (en) View
3326183011	en	Fully specified name (core metadata concept)	Hyperinsulinism due to uncoupling protein 2 deficiency (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3326185016 - Hyperinsulinism due to UCP2 deficiency (en) View
3326185016	en	Synonym (core metadata concept)	Hyperinsulinism due to UCP2 deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
3326186015 - Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency (en) View
3326186015	en	Synonym (core metadata concept)	Hyperinsulinism due to UCP2 (uncoupling protein 2) deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6761145021) - 721834007 -> 83469008 (116680003) View
116680003 \|Is a (attribute)\|	83469008 \|Hyperinsulinism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112445021) - 721834007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12876702022) - 721834007 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16329797020) - 721834007 -> 1363361006 (116680003) View
116680003 \|Is a (attribute)\|	1363361006 \|Diazoxide-sensitive diffuse hyperinsulinism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16329798026) - 721834007 -> 736652002 (116680003) View
116680003 \|Is a (attribute)\|	736652002 \|Neonatal metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16329799023) - 721834007 -> 736653007 (116680003) View
116680003 \|Is a (attribute)\|	736653007 \|Neonatal disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16329800022) - 721834007 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15880908028) - 721834007 -> 42357009 (116680003) View
116680003 \|Is a (attribute)\|	42357009 \|Disorder of digestive system specific to fetus or newborn (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6761148023) - 721834007 -> 78696007 (363698007) View
363698007 \|Finding site (attribute)\|	78696007 \|Endocrine pancreatic structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112446022) - 721834007 -> 78696007 (363698007) View
363698007 \|Finding site (attribute)\|	78696007 \|Endocrine pancreatic structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6761144020) - 721834007 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6761146022) - 721834007 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6761147029) - 721834007 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1363361006 View
1363361006	Diazoxide-sensitive diffuse hyperinsulinism (disorder)	Diazoxide-sensitive diffuse hyperinsulinism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
42357009 View
42357009	Disorder of digestive system specific to fetus or newborn (disorder)	Perinatal digestive system disorders	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
736652002 View
736652002	Neonatal metabolic disorder (disorder)	Neonatal metabolic disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
736653007 View
736653007	Neonatal disorder of endocrine system (disorder)	Neonatal endocrine disorder	900000000000073002 \|Sufficiently defined by necessary conditions 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
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions 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 (795d48b8-e6a6-50e9-8686-24f622b5d548) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E16.1	TRUE	ALWAYS E16.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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 721834007

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches