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Terminology chevron_right Concepts chevron_right 233666007

Production

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Component

233666007

The component that hold information about this concept.

Fully Specified Name (FSN)

Young's syndrome (disorder)

Shortest Term

Young syndrome

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

Young's syndrome (disorder)

SCTID: 233666007, Primitive, Active

233666007|Young's syndrome (disorder)|

vi Hội chứng young (là một tình trạng hiếm gặp bao gồm sự kết hợp của các hội chứng như giãn phế quản, viêm mũi xoang và giảm khả năng sinh sản ở nam giới)
en Azoospermia, obstructive and chronic sinopulmonary infections
en Sinusitis-infertility syndrome
en Young syndrome
en Young's syndrome (disorder)
en Barry-perkins-young syndrome
en Young's syndrome

Expression

233666007 |Young's syndrome (disorder)|
 <<< 86204009 |Immotile cilia syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 321667001 |Respiratory tract structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 260379002 |Impaired (qualifier value)|,
363714003 |Interprets (attribute)| = 63533009 |Mucociliary clearance, function (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
561261000003115 - hội chứng Young (là một tình trạng hiếm gặp bao gồm sự kết hợp của các hội chứng như giãn phế quản, viêm mũi xoang và giảm khả năng sinh sản ở nam giới) (vi) View
561261000003115	vi	Synonym (core metadata concept)	hội chứng Young (là một tình trạng hiếm gặp bao gồm sự kết hợp của các hội chứng như giãn phế quản, viêm mũi xoang và giảm khả năng sinh sản ở nam giới)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
350132013 - Azoospermia, obstructive and chronic sinopulmonary infections (en) View
350132013	en	Synonym (core metadata concept)	Azoospermia, obstructive and chronic sinopulmonary infections	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
350133015 - Sinusitis-infertility syndrome (en) View
350133015	en	Synonym (core metadata concept)	Sinusitis-infertility syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2838642016 - Young syndrome (en) View
2838642016	en	Synonym (core metadata concept)	Young syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
621881011 - Young's syndrome (disorder) (en) View
621881011	en	Fully specified name (core metadata concept)	Young's syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
350134014 - Barry-Perkins-Young syndrome (en) View
350134014	en	Synonym (core metadata concept)	Barry-Perkins-Young syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
350131018 - Young's syndrome (en) View
350131018	en	Synonym (core metadata concept)	Young's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7341100021) - 233666007 -> 6920004 (116676008) View
116676008 \|Associated morphology (attribute)\|	6920004 \|Defect (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7341101020) - 233666007 -> 321667001 (363698007) View
363698007 \|Finding site (attribute)\|	321667001 \|Respiratory tract structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15470345025) - 233666007 -> 321667001 (363698007) View
363698007 \|Finding site (attribute)\|	321667001 \|Respiratory tract structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5020416020) - 233666007 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10525788023) - 233666007 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10525789026) - 233666007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341102029) - 233666007 -> 260379002 (363713009) View
363713009 \|Has interpretation (attribute)\|	260379002 \|Impaired (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7341103023) - 233666007 -> 63533009 (363714003) View
363714003 \|Interprets (attribute)\|	63533009 \|Mucociliary clearance, function (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (510712021) - 233666007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2253384026) - 233666007 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4996873025) - 233666007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (46902029) - 233666007 -> 86204009 (116680003) View
116680003 \|Is a (attribute)\|	86204009 \|Immotile cilia syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
86204009 View
86204009	Immotile cilia syndrome (disorder)	Immotile cilia syndrome	900000000000074008 \|Necessary but not sufficient concept 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 (ee167fb1-b71a-5618-9fa0-cd6ecdefa546) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	TRUE	ALWAYS Q87.8	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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