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Terminology chevron_right Concepts chevron_right 190913009

Production

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Language with ID “c8edd900-6526-5880-a8cd-e7b86ecce280” doesn’t exist. Perhaps it was deleted?

Component

190913009

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital porphyria (disorder)

Shortest Term

Congenital 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

Congenital porphyria (disorder)

SCTID: 190913009, Defined, Active

190913009|Congenital porphyria (disorder)|

en Congenital porphyria
en Congenital porphyria (disorder)

Expression

190913009 |Congenital porphyria (disorder)|
 === 66091009 |Congenital disease (disorder)| + 
403832004 |Inherited disorder of porphyrin metabolism (disorder)| + 
418470004 |Porphyria (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
293541015 - Congenital porphyria (en) View
293541015	en	Synonym (core metadata concept)	Congenital porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
574553012 - Congenital porphyria (disorder) (en) View
574553012	en	Fully specified name (core metadata concept)	Congenital porphyria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (959575023) - 190913009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1693200021) - 190913009 -> 29094004 (116680003) View
116680003 \|Is a (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2845325028) - 190913009 -> 403832004 (116680003) View
116680003 \|Is a (attribute)\|	403832004 \|Inherited disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2845326027) - 190913009 -> 418470004 (116680003) View
116680003 \|Is a (attribute)\|	418470004 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2773784020) - 190913009 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (959576024) - 190913009 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (326080026) - 190913009 -> 238052001 (116680003) View
116680003 \|Is a (attribute)\|	238052001 \|Disorder of porphyrin and heme metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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
403832004 View
403832004	Inherited disorder of porphyrin metabolism (disorder)	Inherited disorder of porphyrin metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
22935002 View
22935002	Congenital erythropoietic porphyria (disorder)	Gunther's disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
51022005 View
51022005	Erythropoietic protoporphyria (disorder)	Epp	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
64081000 View
64081000	Porphobilinogen synthase deficiency (disorder)	Alad deficiency	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 (0b7e1566-30c0-5b3e-a980-b091258b338a) 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)\|
ExtendedMap object (33115c50-00d7-508b-9a01-276832d90168) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	OTHERWISE 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)\|
ExtendedMap object (4e53a558-0887-5602-9bb9-16bd2668547f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.0	IFA 51022005 \| Erythropoietic protoporphyria (disorder) \|	IF ERYTHROPOIETIC PROTOPORPHYRIA CHOOSE E80.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (8eb5c8a5-fe10-5741-b3a1-f250a06cd2f3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.0	IFA 22935002 \| Congenital erythropoietic porphyria (disorder) \|	IF CONGENITAL ERYTHROPOIETIC PORPHYRIA CHOOSE E80.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (9f313358-41a9-56a6-8802-1084f609c881) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	IFA 64081000 \| Porphobilinogen synthase deficiency (disorder) \|	IF PORPHOBILINOGEN SYNTHASE DEFICIENCY CHOOSE E80.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (0b7e1566-30c0-5b3e-a980-b091258b338a) 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)\|
ExtendedMap object (33115c50-00d7-508b-9a01-276832d90168) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	OTHERWISE 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)\|
ExtendedMap object (4e53a558-0887-5602-9bb9-16bd2668547f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.0	IFA 51022005 \| Erythropoietic protoporphyria (disorder) \|	IF ERYTHROPOIETIC PROTOPORPHYRIA CHOOSE E80.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (8eb5c8a5-fe10-5741-b3a1-f250a06cd2f3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.0	IFA 22935002 \| Congenital erythropoietic porphyria (disorder) \|	IF CONGENITAL ERYTHROPOIETIC PORPHYRIA CHOOSE E80.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (9f313358-41a9-56a6-8802-1084f609c881) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E80.2	IFA 64081000 \| Porphobilinogen synthase deficiency (disorder) \|	IF PORPHOBILINOGEN SYNTHASE DEFICIENCY CHOOSE E80.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Terminology chevron_right Concepts chevron_right 190913009

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