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Terminology chevron_right Concepts chevron_right 5655007

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Component

5655007

The component that hold information about this concept.

Fully Specified Name (FSN)

Inherited disorder of bilirubin metabolism (disorder)

Shortest Term

Inherited disorder of bilirubin metabolism

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

Inherited disorder of bilirubin metabolism (disorder)

SCTID: 5655007, Primitive, Active

5655007|Inherited disorder of bilirubin metabolism (disorder)|

en Inherited disorder of bilirubin metabolism
en Inherited disorder of bilirubin metabolism (disorder)

Expression

5655007 |Inherited disorder of bilirubin metabolism (disorder)|
 <<< 80006005 |Disorder of bilirubin metabolism (disorder)| + 
86095007 |Inborn error of metabolism (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
10430013 - Inherited disorder of bilirubin metabolism (en) View
10430013	en	Synonym (core metadata concept)	Inherited disorder of bilirubin metabolism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
795075017 - Inherited disorder of bilirubin metabolism (disorder) (en) View
795075017	en	Fully specified name (core metadata concept)	Inherited disorder of bilirubin metabolism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
10431012 - Inherited disorder of bilirubin metabolism, NOS (en) View
10431012	en	Synonym (core metadata concept)	Inherited disorder of bilirubin metabolism, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (814226023) - 5655007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (240113022) - 5655007 -> 276266002 (116680003) View
116680003 \|Is a (attribute)\|	276266002 \|Disorder of bilirubin metabolism and excretion (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2771266028) - 5655007 -> 86095007 (116680003) View
116680003 \|Is a (attribute)\|	86095007 \|Inborn error of metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (814225022) - 5655007 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (240112028) - 5655007 -> 80006005 (116680003) View
116680003 \|Is a (attribute)\|	80006005 \|Disorder of bilirubin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
80006005 View
80006005	Disorder of bilirubin metabolism (disorder)	Bilirubin metabolism disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
86095007 View
86095007	Inborn error of metabolism (disorder)	Inborn error of metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
720513002 View
720513002	Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder)	Arc (arthrogryposis, renal dysfunction, cholestasis) syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
27503000 View
27503000	Gilbert's syndrome (disorder)	Gilbert syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
62216007 View
62216007	Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder)	Hội chứng gan thận ứ mật - cứng khớp gia đình	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
28259009 View
28259009	Crigler-najjar syndrome (disorder)	Crigler-najjar syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
32891000 View
32891000	Rotor syndrome (disorder)	Rotor syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
44553005 View
44553005	Dubin-johnson syndrome (disorder)	Spinz-nelson syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (3cd481dc-1234-5ba7-b315-feb17476b68b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.6	TRUE	ALWAYS E80.6	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 5655007

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