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Terminology chevron_right Concepts chevron_right 55056006

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Component

55056006

The component that hold information about this concept.

Fully Specified Name (FSN)

Hepatic porphyria (disorder)

Shortest Term

Hepatic 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

Hepatic porphyria (disorder)

SCTID: 55056006, Defined, Active

55056006|Hepatic porphyria (disorder)|

vi Rối loạn chuyển hóa porphyrin ở gan
en Hepatic porphyria
en Hepatic porphyria (disorder)

Expression

55056006 |Hepatic porphyria (disorder)|
 === 235856003 |Disorder of liver (disorder)| + 
418470004 |Porphyria (disorder)| : 
        { 363698007 |Finding site (attribute)| = 10200004 |Liver structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
445691000003114 - rối loạn chuyển hóa porphyrin ở gan (vi) View
445691000003114	vi	Synonym (core metadata concept)	rối loạn chuyển hóa porphyrin ở gan	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
91537011 - Hepatic porphyria (en) View
91537011	en	Synonym (core metadata concept)	Hepatic porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
793355018 - Hepatic porphyria (disorder) (en) View
793355018	en	Fully specified name (core metadata concept)	Hepatic porphyria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
91538018 - Hepatic porphyria, NOS (en) View
91538018	en	Synonym (core metadata concept)	Hepatic porphyria, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (810595022) - 55056006 -> 10200004 (363698007) View
363698007 \|Finding site (attribute)\|	10200004 \|Liver structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1677706023) - 55056006 -> 29094004 (116680003) View
116680003 \|Is a (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2842388024) - 55056006 -> 418470004 (116680003) View
116680003 \|Is a (attribute)\|	418470004 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (237627028) - 55056006 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (810596023) - 55056006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (237626021) - 55056006 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (237629025) - 55056006 -> 69518005 (116680003) View
116680003 \|Is a (attribute)\|	69518005 \|Congenital anomaly of digestive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (237630024) - 55056006 -> 86292002 (116680003) View
116680003 \|Is a (attribute)\|	86292002 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (237628022) - 55056006 -> 235856003 (116680003) View
116680003 \|Is a (attribute)\|	235856003 \|Disorder of liver (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
418470004 View
418470004	Porphyria (disorder)	Porphyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
235856003 View
235856003	Disorder of liver (disorder)	Bệnh gan	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
7425008 View
7425008	Hereditary coproporphyria (disorder)	Cpo deficiency	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
58275005 View
58275005	Variegate porphyria (disorder)	Mixed porphyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
61860000 View
61860000	Porphyria cutanea tarda (disorder)	Pct	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 (bd0342cc-9154-59cc-a484-1ebb58c1f9d2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	TRUE	ALWAYS E80.2 \| 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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