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Terminology chevron_right Concepts chevron_right 342553006

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Periodic hyperlysinemia with hyperammonemia (disorder)

Shortest Term

Hyperlysinuria with hyperammonemia

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Periodic hyperlysinemia with hyperammonemia (disorder)

SCTID: 342553006, Primitive, Active

342553006|Periodic hyperlysinemia with hyperammonemia (disorder)|

Expression

342553006 |Periodic hyperlysinemia with hyperammonemia (disorder)|
 <<< 58558003 |Hyperlysinemia (disorder)| + 
9360008 |Hyperammonemia (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
470311013 - Hyperlysinuria with hyperammonaemia (en) View
470311013	en	Synonym (core metadata concept)	Hyperlysinuria with hyperammonaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
470309016 - Hyperlysinuria with hyperammonemia (en) View
470309016	en	Synonym (core metadata concept)	Hyperlysinuria with hyperammonemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
470310014 - Periodic hyperlysinaemia with hyperammonaemia (en) View
470310014	en	Synonym (core metadata concept)	Periodic hyperlysinaemia with hyperammonaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
470312018 - Periodic hyperlysinemia with hyperammonemia (en) View
470312018	en	Synonym (core metadata concept)	Periodic hyperlysinemia with hyperammonemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
723958019 - Periodic hyperlysinemia with hyperammonemia (disorder) (en) View
723958019	en	Fully specified name (core metadata concept)	Periodic hyperlysinemia with hyperammonemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16400890026) - 342553006 -> 9360008 (116680003) View
116680003 \|Is a (attribute)\|	9360008 \|Hyperammonemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (687712028) - 342553006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (687711024) - 342553006 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (153369029) - 342553006 -> 58558003 (116680003) View
116680003 \|Is a (attribute)\|	58558003 \|Hyperlysinemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
9360008 View
9360008	Hyperammonemia (disorder)	Hyperammonemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
58558003 View
58558003	Hyperlysinemia (disorder)	Hyperlysinemia	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 (6896645c-5962-575d-8dc9-d06315e7d9e3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.3	TRUE	ALWAYS E72.3	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)\|

Descriptions