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Terminology chevron_right Concepts chevron_right 206458002

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Component

206458002

The component that hold information about this concept.

Fully Specified Name (FSN)

Neonatal jaundice with porphyria (disorder)

Shortest Term

Neonatal jaundice with porphyria

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 jaundice with porphyria (disorder)

SCTID: 206458002, Defined, Active

206458002|Neonatal jaundice with porphyria (disorder)|

en Neonatal jaundice with porphyria
en Neonatal jaundice with porphyria (disorder)

Expression

206458002 |Neonatal jaundice with porphyria (disorder)|
 === 387712008 |Neonatal jaundice (disorder)| + 
736652002 |Neonatal metabolic disorder (disorder)| + 
418470004 |Porphyria (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        { 42752001 |Due to (attribute)| = 418470004 |Porphyria (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
316626013 - Neonatal jaundice with porphyria (en) View
316626013	en	Synonym (core metadata concept)	Neonatal jaundice with porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
591955016 - Neonatal jaundice with porphyria (disorder) (en) View
591955016	en	Fully specified name (core metadata concept)	Neonatal jaundice with porphyria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (11572446027) - 206458002 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11572447020) - 206458002 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065942023) - 206458002 -> 707861009 (363698007) View
363698007 \|Finding site (attribute)\|	707861009 \|Structure of skin and/or skin-associated mucous membrane (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065943029) - 206458002 -> 14783006 (42752001) View
42752001 \|Due to (attribute)\|	14783006 \|Hyperbilirubinemia (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065944024) - 206458002 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065945020) - 206458002 -> 18619003 (363698007) View
363698007 \|Finding site (attribute)\|	18619003 \|Scleral structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14967906027) - 206458002 -> 29094004 (116680003) View
116680003 \|Is a (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15785677020) - 206458002 -> 418470004 (42752001) View
42752001 \|Due to (attribute)\|	418470004 \|Porphyria (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15798449020) - 206458002 -> 418470004 (116680003) View
116680003 \|Is a (attribute)\|	418470004 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14967907020) - 206458002 -> 736652002 (116680003) View
116680003 \|Is a (attribute)\|	736652002 \|Neonatal metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2875143027) - 206458002 -> 29094004 (47429007) View
47429007 \|Associated with (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12065946021) - 206458002 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (972853028) - 206458002 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2743671028) - 206458002 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2743672024) - 206458002 -> 61860000 (47429007) View
47429007 \|Associated with (attribute)\|	61860000 \|Porphyria cutanea tarda (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1791885027) - 206458002 -> 303270005 (363698007) View
363698007 \|Finding site (attribute)\|	303270005 \|Liver and/or biliary structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1791884028) - 206458002 -> 371578004 (246454002) View
246454002 \|Occurrence (attribute)\|	371578004 \|Perinatal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972849025) - 206458002 -> 118971007 (363698007) View
363698007 \|Finding site (attribute)\|	118971007 \|Digestive system subdivision (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (331366021) - 206458002 -> 111470007 (116680003) View
116680003 \|Is a (attribute)\|	111470007 \|Neonatal jaundice (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972851026) - 206458002 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1939643026) - 206458002 -> 387712008 (116680003) View
116680003 \|Is a (attribute)\|	387712008 \|Neonatal jaundice (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (972848022) - 206458002 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972850025) - 206458002 -> 57855005 (246454002) View
246454002 \|Occurrence (attribute)\|	57855005 \|Perinatal state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (972852022) - 206458002 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	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
418470004 View
418470004	Porphyria (disorder)	Porphyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
387712008 View
387712008	Neonatal jaundice (disorder)	Vàng da sơ sinh	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 (1aec72ad-55c4-57c7-9a76-bf406b8392b8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P59.9	TRUE	ALWAYS P59.9 \| MAPPED FOLLOWING WHO GUIDANCE	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 (9b50a00e-e2e2-5a1f-af13-c75649ee536d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	TRUE	ALWAYS E80.2 \| MAPPED FOLLOWING WHO GUIDANCE \| POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE	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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