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Terminology chevron_right Concepts chevron_right 405769009

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Component

405769009

The component that hold information about this concept.

Fully Specified Name (FSN)

Klinefelter's syndrome, xxy (disorder)

Shortest Term

Xxy 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

Klinefelter's syndrome, xxy (disorder)

SCTID: 405769009, Primitive, Active

405769009|Klinefelter's syndrome, xxy (disorder)|

en Klinefelter's syndrome karyotype 47 xxy
en Klinefelter's syndrome, xxy
en Klinefelter's syndrome, xxy (disorder)
en Klinefelter syndrome, xxy
en Xxy klinefelter's syndrome
en Xxy syndrome

Expression

405769009 |Klinefelter's syndrome, xxy (disorder)|
 <<< 22053006 |Klinefelter syndrome (disorder)|
        { 116676008 |Associated morphology (attribute)| = 41669009 |Alteration of chromosome structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 72837006 |Sex chromosome x (cell structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2163147012 - Klinefelter's syndrome (en) View
2163147012	en	Synonym (core metadata concept)	Klinefelter's syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
2163150010 - Klinefelter's syndrome karyotype 47 XXY (en) View
2163150010	en	Synonym (core metadata concept)	Klinefelter's syndrome karyotype 47 XXY	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2157545011 - Klinefelter's syndrome, XXY (en) View
2157545011	en	Synonym (core metadata concept)	Klinefelter's syndrome, XXY	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
2149599019 - Klinefelter's syndrome, XXY (disorder) (en) View
2149599019	en	Fully specified name (core metadata concept)	Klinefelter's syndrome, XXY (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
2163149010 - Klinefelter syndrome (en) View
2163149010	en	Synonym (core metadata concept)	Klinefelter syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
2838565019 - Klinefelter syndrome, XXY (en) View
2838565019	en	Synonym (core metadata concept)	Klinefelter syndrome, XXY	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2163151014 - XXY Klinefelter's syndrome (en) View
2163151014	en	Synonym (core metadata concept)	XXY Klinefelter's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2163148019 - XXY syndrome (en) View
2163148019	en	Synonym (core metadata concept)	XXY syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2559068020) - 405769009 -> 268300003 (116680003) View
116680003 \|Is a (attribute)\|	268300003 \|Klinefelter's syndrome - male with more than two x chromosomes (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5008406021) - 405769009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010982021) - 405769009 -> 107673000 (116676008) View
116676008 \|Associated morphology (attribute)\|	107673000 \|Cellular and/or subcellular abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010983027) - 405769009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6019254020) - 405769009 -> 22053006 (116680003) View
116680003 \|Is a (attribute)\|	22053006 \|Klinefelter syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6019255021) - 405769009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6019256022) - 405769009 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6019257029) - 405769009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2495871020) - 405769009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3448091027) - 405769009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3397552029) - 405769009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2495872029) - 405769009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2621569024) - 405769009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2467330029) - 405769009 -> 405770005 (116680003) View
116680003 \|Is a (attribute)\|	405770005 \|Klinefelter's syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2495870021) - 405769009 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
22053006 View
22053006	Klinefelter syndrome (disorder)	Xxy 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 (082d298c-cda0-5b6a-bb6e-d9a540ea6dce) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q98.1	TRUE	ALWAYS Q98.1	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)\|
ExtendedMap object (e1e33beb-7c40-547c-bf83-ba549de1394e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q98.0	TRUE	ALWAYS Q98.0	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)\|

Terminology chevron_right Concepts chevron_right 405769009

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