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Terminology chevron_right Concepts chevron_right 206457007

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Component

206457007

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal jaundice with congenital hypothyroidism (disorder)

Shortest Term

Neonatal jaundice with congenital hypothyroidism

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Neonatal jaundice with congenital hypothyroidism (disorder)

SCTID: 206457007, Defined, Active

206457007|Neonatal jaundice with congenital hypothyroidism (disorder)|

en Neonatal jaundice with congenital hypothyroidism
en Neonatal jaundice with congenital hypothyroidism (disorder)

Expression

206457007 |Neonatal jaundice with congenital hypothyroidism (disorder)|
 === 387712008 |Neonatal jaundice (disorder)| + 
190268003 |Congenital hypothyroidism (disorder)| + 
405629002 |Infant hypothyroidism (disorder)| + 
22925008 |Neonatal disorder (disorder)| : 
        { 42752001 |Due to (attribute)| = 190268003 |Congenital hypothyroidism (disorder)| }
        { 246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 69748006 |Thyroid structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
316625012 - Neonatal jaundice with congenital hypothyroidism (en) View
316625012	en	Synonym (core metadata concept)	Neonatal jaundice with congenital hypothyroidism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
591954017 - Neonatal jaundice with congenital hypothyroidism (disorder) (en) View
591954017	en	Fully specified name (core metadata concept)	Neonatal jaundice with congenital hypothyroidism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11575717029) - 206457007 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12066552022) - 206457007 -> 14783006 (42752001) View
42752001 \|Due to (attribute)\|	14783006 \|Hyperbilirubinemia (disorder)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12066553028) - 206457007 -> 18619003 (363698007) View
363698007 \|Finding site (attribute)\|	18619003 \|Scleral structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12066554023) - 206457007 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12066555024) - 206457007 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12066556020) - 206457007 -> 707861009 (363698007) View
363698007 \|Finding site (attribute)\|	707861009 \|Structure of skin and/or skin-associated mucous membrane (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14975736026) - 206457007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14975737024) - 206457007 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15798446029) - 206457007 -> 22925008 (116680003) View
116680003 \|Is a (attribute)\|	22925008 \|Neonatal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15798447022) - 206457007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15798448028) - 206457007 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2743670027) - 206457007 -> 190268003 (47429007) View
47429007 \|Associated with (attribute)\|	190268003 \|Congenital hypothyroidism (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14967902025) - 206457007 -> 190268003 (42752001) View
42752001 \|Due to (attribute)\|	190268003 \|Congenital hypothyroidism (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14975734028) - 206457007 -> 190268003 (116680003) View
116680003 \|Is a (attribute)\|	190268003 \|Congenital hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14975735027) - 206457007 -> 405629002 (116680003) View
116680003 \|Is a (attribute)\|	405629002 \|Infant hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (972842023) - 206457007 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2743669028) - 206457007 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11575718023) - 206457007 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1791882029) - 206457007 -> 303270005 (363698007) View
363698007 \|Finding site (attribute)\|	303270005 \|Liver and/or biliary structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1791883023) - 206457007 -> 371578004 (246454002) View
246454002 \|Occurrence (attribute)\|	371578004 \|Perinatal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2556712021) - 206457007 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2615878028) - 206457007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972846021) - 206457007 -> 118971007 (363698007) View
363698007 \|Finding site (attribute)\|	118971007 \|Digestive system subdivision (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (331365020) - 206457007 -> 111470007 (116680003) View
116680003 \|Is a (attribute)\|	111470007 \|Neonatal jaundice (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972844024) - 206457007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1939642020) - 206457007 -> 387712008 (116680003) View
116680003 \|Is a (attribute)\|	387712008 \|Neonatal jaundice (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (972843029) - 206457007 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972845020) - 206457007 -> 57855005 (246454002) View
246454002 \|Occurrence (attribute)\|	57855005 \|Perinatal state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972847028) - 206457007 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
190268003 View
190268003	Congenital hypothyroidism (disorder)	Congenital hypothyroidism	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
387712008 View
387712008	Neonatal jaundice (disorder)	Vàng da sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
22925008 View
22925008	Neonatal disorder (disorder)	Neonatal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
405629002 View
405629002	Infant hypothyroidism (disorder)	Infant hypothyroidism	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 (4d2ab016-ee3c-5a60-bdf5-127bd83726cc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P59.9	TRUE	ALWAYS P59.9	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)\|
ExtendedMap object (5037bf15-d959-5801-906c-4a531ffe057f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E03.1	TRUE	ALWAYS E03.1	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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