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Terminology chevron_right Concepts chevron_right 764955006

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Component

764955006

The component that hold information about this concept.

Fully Specified Name (FSN)

Laubry pezzi syndrome (disorder)

Shortest Term

Laubry pezzi 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

Laubry pezzi syndrome (disorder)

SCTID: 764955006, Primitive, Active

764955006|Laubry pezzi syndrome (disorder)|

en Laubry pezzi syndrome
en Laubry pezzi syndrome (disorder)
en Ventricular septal defect with aortic insufficiency

Expression

764955006 |Laubry pezzi syndrome (disorder)|
 <<< 447822009 |Congenital prolapse of aortic valve (disorder)| + 
768552007 |Congenital ventricular septal defect (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 783804002 |Abnormal communication (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 589001 |Interventricular septum structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 29696001 |Prolapse (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 34202007 |Aortic valve structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3655763018 - Laubry Pezzi syndrome (en) View
3655763018	en	Synonym (core metadata concept)	Laubry Pezzi syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3655761016 - Laubry Pezzi syndrome (disorder) (en) View
3655761016	en	Fully specified name (core metadata concept)	Laubry Pezzi syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3655762011 - Ventricular septal defect with aortic insufficiency (en) View
3655762011	en	Synonym (core metadata concept)	Ventricular septal defect with aortic insufficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9225111025) - 764955006 -> 371520008 (116676008) View
116676008 \|Associated morphology (attribute)\|	371520008 \|Developmental failure of fusion (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15495022020) - 764955006 -> 783804002 (116676008) View
116676008 \|Associated morphology (attribute)\|	783804002 \|Abnormal communication (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204014023) - 764955006 -> 61989004 (116676008) View
116676008 \|Associated morphology (attribute)\|	61989004 \|Congenital prolapse (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10522476027) - 764955006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10522477020) - 764955006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11168558026) - 764955006 -> 29696001 (116676008) View
116676008 \|Associated morphology (attribute)\|	29696001 \|Prolapse (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204013028) - 764955006 -> 447822009 (116680003) View
116680003 \|Is a (attribute)\|	447822009 \|Congenital prolapse of aortic valve (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204015024) - 764955006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9204016020) - 764955006 -> 34202007 (363698007) View
363698007 \|Finding site (attribute)\|	34202007 \|Aortic valve structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9225112021) - 764955006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9225113027) - 764955006 -> 589001 (363698007) View
363698007 \|Finding site (attribute)\|	589001 \|Interventricular septum structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9535738026) - 764955006 -> 768552007 (116680003) View
116680003 \|Is a (attribute)\|	768552007 \|Congenital ventricular septal defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
768552007 View
768552007	Congenital ventricular septal defect (disorder)	Congenital ventricular septal defect	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
447822009 View
447822009	Congenital prolapse of aortic valve (disorder)	Congenital aortic valvar prolapse	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 (6200ef76-ace3-5ddd-8f0c-13ea29b7ddf8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q21.0	TRUE	ALWAYS Q21.0 \| 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)\|

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