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Terminology chevron_right Concepts chevron_right 6160004

Production

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Component

6160004

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal hemochromatosis (disorder)

Shortest Term

Neonatal hemochromatosis

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

Neonatal hemochromatosis (disorder)

SCTID: 6160004, Defined, Active

6160004|Neonatal hemochromatosis (disorder)|

en Idiopathic neonatal haemochromatosis
en Idiopathic neonatal hemochromatosis
en Neonatal haemochromatosis
en Neonatal hemochromatosis
en Neonatal hemochromatosis (disorder)

Expression

6160004 |Neonatal hemochromatosis (disorder)|
 === 399187006 |Hemochromatosis (disorder)| + 
736652002 |Neonatal metabolic disorder (disorder)| : 
        { 246075003 |Causative agent (attribute)| = 767270007 |Iron and iron compound (substance)| }
        { 246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
499063010 - Idiopathic neonatal haemochromatosis (en) View
499063010	en	Synonym (core metadata concept)	Idiopathic neonatal haemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
499062017 - Idiopathic neonatal hemochromatosis (en) View
499062017	en	Synonym (core metadata concept)	Idiopathic neonatal hemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
499064016 - Neonatal haemochromatosis (en) View
499064016	en	Synonym (core metadata concept)	Neonatal haemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
11239018 - Neonatal hemochromatosis (en) View
11239018	en	Synonym (core metadata concept)	Neonatal hemochromatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
800680010 - Neonatal hemochromatosis (disorder) (en) View
800680010	en	Fully specified name (core metadata concept)	Neonatal hemochromatosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
499061012 - Neonatal giant cell hepatitis (en) View
499061012	en	Synonym (core metadata concept)	Neonatal giant cell hepatitis	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2735205028) - 6160004 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9327672028) - 6160004 -> 767270007 (246075003) View
246075003 \|Causative agent (attribute)\|	767270007 \|Iron and iron compound (substance)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2866511027) - 6160004 -> 105840005 (246075003) View
246075003 \|Causative agent (attribute)\|	105840005 \|Iron and/or iron compound (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2694720025) - 6160004 -> 22925008 (116680003) View
116680003 \|Is a (attribute)\|	22925008 \|Neonatal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7239294029) - 6160004 -> 736652002 (116680003) View
116680003 \|Is a (attribute)\|	736652002 \|Neonatal metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (827479020) - 6160004 -> 3829006 (246075003) View
246075003 \|Causative agent (attribute)\|	3829006 \|Iron (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (248263023) - 6160004 -> 276551001 (116680003) View
116680003 \|Is a (attribute)\|	276551001 \|Perinatal hepatitis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (827480023) - 6160004 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1773084028) - 6160004 -> 371578004 (246454002) View
246454002 \|Occurrence (attribute)\|	371578004 \|Perinatal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2598960026) - 6160004 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268611024) - 6160004 -> 118971007 (363698007) View
363698007 \|Finding site (attribute)\|	118971007 \|Digestive system subdivision (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (248264028) - 6160004 -> 86781004 (116680003) View
116680003 \|Is a (attribute)\|	86781004 \|Hemochromatosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2229774022) - 6160004 -> 399187006 (116680003) View
116680003 \|Is a (attribute)\|	399187006 \|Hemochromatosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (827478028) - 6160004 -> 118971007 (363698007) View
363698007 \|Finding site (attribute)\|	118971007 \|Digestive system subdivision (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (827481022) - 6160004 -> 57855005 (246454002) View
246454002 \|Occurrence (attribute)\|	57855005 \|Perinatal state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
736652002 View
736652002	Neonatal metabolic disorder (disorder)	Neonatal metabolic disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
399187006 View
399187006	Hemochromatosis (disorder)	Hemochromatosis	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 (0ef007c9-3182-559b-bceb-e873e8be82cc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.1	TRUE	ALWAYS E83.1	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)\|

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