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Terminology chevron_right Concepts chevron_right 276565004

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Attribute Value with ID “fccc95a7-d7b3-5cdc-bf44-a9cef48605ac” doesn’t exist. Perhaps it was deleted?

Component

276565004

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal goiter (disorder)

Shortest Term

Neonatal goiter

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 goiter (disorder)

SCTID: 276565004, Defined, Active

276565004|Neonatal goiter (disorder)|

en Neonatal goiter
en Neonatal goiter (disorder)
en Neonatal goitre

Expression

276565004 |Neonatal goiter (disorder)|
 === 3716002 |Goiter (disorder)| + 
736653007 |Neonatal disorder of endocrine system (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 442021009 |Enlargement (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181117000 |Entire thyroid gland (body structure)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
412758012 - Neonatal goiter (en) View
412758012	en	Synonym (core metadata concept)	Neonatal goiter	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
669495018 - Neonatal goiter (disorder) (en) View
669495018	en	Fully specified name (core metadata concept)	Neonatal goiter (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
412759016 - Neonatal goitre (en) View
412759016	en	Synonym (core metadata concept)	Neonatal goitre	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2756711028) - 276565004 -> 22925008 (116680003) View
116680003 \|Is a (attribute)\|	22925008 \|Neonatal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663219027) - 276565004 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663220022) - 276565004 -> 181117000 (363698007) View
363698007 \|Finding site (attribute)\|	181117000 \|Entire thyroid gland (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13649406028) - 276565004 -> 736653007 (116680003) View
116680003 \|Is a (attribute)\|	736653007 \|Neonatal disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13649407021) - 276565004 -> 181117000 (363698007) View
363698007 \|Finding site (attribute)\|	181117000 \|Entire thyroid gland (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13649408027) - 276565004 -> 442021009 (116676008) View
116676008 \|Associated morphology (attribute)\|	442021009 \|Enlargement (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2716727020) - 276565004 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3385186029) - 276565004 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3385187022) - 276565004 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (94032020) - 276565004 -> 276564000 (116680003) View
116680003 \|Is a (attribute)\|	276564000 \|Perinatal fetal and/or neonatal thyroid disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (599836025) - 276565004 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2855278024) - 276565004 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1739178029) - 276565004 -> 371578004 (246454002) View
246454002 \|Occurrence (attribute)\|	371578004 \|Perinatal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (599835026) - 276565004 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (599837023) - 276565004 -> 57855005 (246454002) View
246454002 \|Occurrence (attribute)\|	57855005 \|Perinatal state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (94033026) - 276565004 -> 3716002 (116680003) View
116680003 \|Is a (attribute)\|	3716002 \|Goiter (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
736653007 View
736653007	Neonatal disorder of endocrine system (disorder)	Neonatal endocrine disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
3716002 View
3716002	Goiter (disorder)	Goiter	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
59957008 View
59957008	Neonatal graves' disease (disorder)	Neonatal graves' disease	900000000000073002 \|Sufficiently defined by necessary conditions 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 (b949a7e4-cafe-5e79-8332-647acaffb8ac) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P72.0	TRUE	ALWAYS P72.0	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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