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Terminology chevron_right Concepts chevron_right 47444008

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Component

47444008

The component that hold information about this concept.

Fully Specified Name (FSN)

Lucey-driscoll syndrome (disorder)

Shortest Term

Lucey-driscoll 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

Lucey-driscoll syndrome (disorder)

SCTID: 47444008, Primitive, Active

47444008|Lucey-driscoll syndrome (disorder)|

en Transient familial neonatal hyperbilirubinaemia
en Transient familial neonatal hyperbilirubinemia
en Lucey-driscoll syndrome (disorder)
en Lucey-driscoll syndrome

Expression

47444008 |Lucey-driscoll syndrome (disorder)|
 <<< 387712008 |Neonatal jaundice (disorder)| + 
22925008 |Neonatal disorder (disorder)| + 
414032001 |Disorder of pigmentation (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 74571009 |Bile pigmentation (morphologic abnormality)|,
246454002 |Occurrence (attribute)| = 255407002 |Neonatal (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
494832012 - Transient familial neonatal hyperbilirubinaemia (en) View
494832012	en	Synonym (core metadata concept)	Transient familial neonatal hyperbilirubinaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
494833019 - Transient familial neonatal hyperbilirubinemia (en) View
494833019	en	Synonym (core metadata concept)	Transient familial neonatal hyperbilirubinemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
784903018 - Lucey-Driscoll syndrome (disorder) (en) View
784903018	en	Fully specified name (core metadata concept)	Lucey-Driscoll syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
79103017 - Lucey-Driscoll syndrome (en) View
79103017	en	Synonym (core metadata concept)	Lucey-Driscoll syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15799819024) - 47444008 -> 362975008 (116680003) View
116680003 \|Is a (attribute)\|	362975008 \|Degenerative disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12086697029) - 47444008 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12086698023) - 47444008 -> 18619003 (363698007) View
363698007 \|Finding site (attribute)\|	18619003 \|Scleral structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12086699026) - 47444008 -> 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 (12086700025) - 47444008 -> 14783006 (42752001) View
42752001 \|Due to (attribute)\|	14783006 \|Hyperbilirubinemia (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12086701026) - 47444008 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15799817021) - 47444008 -> 22925008 (116680003) View
116680003 \|Is a (attribute)\|	22925008 \|Neonatal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15799820029) - 47444008 -> 414032001 (116680003) View
116680003 \|Is a (attribute)\|	414032001 \|Disorder of pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15799821025) - 47444008 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (791146029) - 47444008 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2733363021) - 47444008 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11457192024) - 47444008 -> 74571009 (116676008) View
116676008 \|Associated morphology (attribute)\|	74571009 \|Bile pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11457193025) - 47444008 -> 255407002 (246454002) View
246454002 \|Occurrence (attribute)\|	255407002 \|Neonatal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1768485021) - 47444008 -> 303270005 (363698007) View
363698007 \|Finding site (attribute)\|	303270005 \|Liver and/or biliary structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1768484020) - 47444008 -> 371578004 (246454002) View
246454002 \|Occurrence (attribute)\|	371578004 \|Perinatal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (791143021) - 47444008 -> 118971007 (363698007) View
363698007 \|Finding site (attribute)\|	118971007 \|Digestive system subdivision (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (225309025) - 47444008 -> 111470007 (116680003) View
116680003 \|Is a (attribute)\|	111470007 \|Neonatal jaundice (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (791141023) - 47444008 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2031701022) - 47444008 -> 387712008 (116680003) View
116680003 \|Is a (attribute)\|	387712008 \|Neonatal jaundice (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (791142027) - 47444008 -> 57855005 (246454002) View
246454002 \|Occurrence (attribute)\|	57855005 \|Perinatal state (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (791144026) - 47444008 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (791145025) - 47444008 -> 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
387712008 View
387712008	Neonatal jaundice (disorder)	Vàng da sơ sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
414032001 View
414032001	Disorder of pigmentation (disorder)	Disorder of pigmentation	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
22925008 View
22925008	Neonatal disorder (disorder)	Neonatal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	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 (d584d9eb-c8fa-5dcd-82e7-04548c414493) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	P59.8	TRUE	ALWAYS P59.8	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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