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Terminology chevron_right Concepts chevron_right 1234996002

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Component

1234996002

The component that hold information about this concept.

Fully Specified Name (FSN)

Fetal disorder due to velamentous insertion of umbilical cord (disorder)

Shortest Term

Fetal disorder due to velamentous insertion of umbilical cord

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

Fetal disorder due to velamentous insertion of umbilical cord (disorder)

SCTID: 1234996002, Defined, Active

1234996002|Fetal disorder due to velamentous insertion of umbilical cord (disorder)|

en Fetal disorder due to velamentous insertion of umbilical cord
en Fetal disorder due to velamentous insertion of umbilical cord (disorder)

Expression

1234996002 |Fetal disorder due to velamentous insertion of umbilical cord (disorder)|
 === 1234959006 |Fetal disorder due to umbilical cord disorder (disorder)| + 
1237255000 |Fetal disorder due to anomaly of placenta (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 303112003 |Fetal period (qualifier value)| }
        { 42752001 |Due to (attribute)| = 77278008 |Velamentous insertion of umbilical cord (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5084924012 - Fetal disorder due to velamentous insertion of umbilical cord (en) View
5084924012	en	Synonym (core metadata concept)	Fetal disorder due to velamentous insertion of umbilical cord	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5084925013 - Fetal disorder due to velamentous insertion of umbilical cord (disorder) (en) View
5084925013	en	Fully specified name (core metadata concept)	Fetal disorder due to velamentous insertion of umbilical cord (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15291989021) - 1234996002 -> 1237255000 (116680003) View
116680003 \|Is a (attribute)\|	1237255000 \|Fetal disorder due to anomaly of placenta (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15881248022) - 1234996002 -> 1269102002 (116680003) View
116680003 \|Is a (attribute)\|	1269102002 \|Fetal disorder due to maternal disorder during pregnancy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15552280028) - 1234996002 -> 1269073009 (116680003) View
116680003 \|Is a (attribute)\|	1269073009 \|Fetal disorder due to disorder of amniotic cavity and/or membrane (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15267670021) - 1234996002 -> 1234959006 (116680003) View
116680003 \|Is a (attribute)\|	1234959006 \|Fetal disorder due to umbilical cord disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15267671020) - 1234996002 -> 77278008 (42752001) View
42752001 \|Due to (attribute)\|	77278008 \|Velamentous insertion of umbilical cord (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15267672029) - 1234996002 -> 303112003 (246454002) View
246454002 \|Occurrence (attribute)\|	303112003 \|Fetal period (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1234959006 View
1234959006	Fetal disorder due to umbilical cord disorder (disorder)	Fetal disorder due to umbilical cord disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1237255000 View
1237255000	Fetal disorder due to anomaly of placenta (disorder)	Fetal disorder due to anomaly of placenta	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 (000f9add-b636-5c52-8862-c78bf4e25a10) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P02.2	TRUE	ALWAYS P02.2 \| 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)\|
ExtendedMap object (359a2e62-419c-5ded-a2fa-a57ef9efea9e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P02.6	TRUE	ALWAYS P02.6 \| 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)\|

Terminology chevron_right Concepts chevron_right 1234996002

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