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Terminology chevron_right Concepts chevron_right 403832004

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Component

403832004

The component that hold information about this concept.

Fully Specified Name (FSN)

Inherited disorder of porphyrin metabolism (disorder)

Shortest Term

Inherited disorder of porphyrin 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 porphyrin metabolism (disorder)

SCTID: 403832004, Primitive, Active

403832004|Inherited disorder of porphyrin metabolism (disorder)|

en Inherited disorder of porphyrin metabolism
en Inherited disorder of porphyrin metabolism (disorder)

Expression

403832004 |Inherited disorder of porphyrin metabolism (disorder)|
 <<< 29094004 |Disorder of porphyrin metabolism (disorder)| + 
1821000146108 |Hereditary metabolic disease (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1782836013 - Inherited disorder of porphyrin metabolism (en) View
1782836013	en	Synonym (core metadata concept)	Inherited disorder of porphyrin metabolism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1771758010 - Inherited disorder of porphyrin metabolism (disorder) (en) View
1771758010	en	Fully specified name (core metadata concept)	Inherited disorder of porphyrin metabolism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12251889027) - 403832004 -> 32895009 (116680003) View
116680003 \|Is a (attribute)\|	32895009 \|Hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15281260028) - 403832004 -> 1821000146108 (116680003) View
116680003 \|Is a (attribute)\|	1821000146108 \|Hereditary metabolic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2291261020) - 403832004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2291260021) - 403832004 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2250518022) - 403832004 -> 29094004 (116680003) View
116680003 \|Is a (attribute)\|	29094004 \|Disorder of porphyrin metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1821000146108 View
1821000146108	Hereditary metabolic disease (disorder)	Hereditary metabolic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
29094004 View
29094004	Disorder of porphyrin metabolism (disorder)	Disorder of porphyrin metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
48983004 View
48983004	X chromosome-linked sideroblastic anemia	X-linked sideroblastic anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
190913009 View
190913009	Congenital porphyria (disorder)	Congenital porphyria	900000000000073002 \|Sufficiently defined by necessary conditions 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 (ed95dfb6-f78c-55d7-b280-3485484166a3) 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)\|

Terminology chevron_right Concepts chevron_right 403832004

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