dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 234422006

Production

add

Component

234422006

The component that hold information about this concept.

Fully Specified Name (FSN)

Acute intermittent porphyria (disorder)

Shortest Term

Acute porphyria

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

Acute intermittent porphyria (disorder)

SCTID: 234422006, Primitive, Active

234422006|Acute intermittent porphyria (disorder)|

en Acute intermittent porphyria
en Acute intermittent porphyria (disorder)
en Acute porphyria
en Intermittent acute porphyria
en Intermittent acute porphyria syndrome
en Pyrroloporphyria
en Aip - acute intermittent porphyria
en Swedish porphyria

Expression

234422006 |Acute intermittent porphyria (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
276263005 |Porphobilinogen deaminase deficiency (disorder)| + 
418470004 |Porphyria (disorder)| : 
        { 263502005 |Clinical course (attribute)| = 7087005 |Intermittent (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
351223014 - Acute intermittent porphyria (en) View
351223014	en	Synonym (core metadata concept)	Acute intermittent porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
622738015 - Acute intermittent porphyria (disorder) (en) View
622738015	en	Fully specified name (core metadata concept)	Acute intermittent porphyria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
351226018 - Acute porphyria (en) View
351226018	en	Synonym (core metadata concept)	Acute porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
351227010 - Intermittent acute porphyria (en) View
351227010	en	Synonym (core metadata concept)	Intermittent acute porphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
351229013 - Intermittent acute porphyria syndrome (en) View
351229013	en	Synonym (core metadata concept)	Intermittent acute porphyria syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
351225019 - Pyrroloporphyria (en) View
351225019	en	Synonym (core metadata concept)	Pyrroloporphyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
351224015 - AIP - Acute intermittent porphyria (en) View
351224015	en	Synonym (core metadata concept)	AIP - Acute intermittent porphyria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
351228017 - Swedish porphyria (en) View
351228017	en	Synonym (core metadata concept)	Swedish porphyria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (1655670023) - 234422006 -> 128289001 (116680003) View
116680003 \|Is a (attribute)\|	128289001 \|Chronic metabolic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3022871023) - 234422006 -> 7087005 (263502005) View
263502005 \|Clinical course (attribute)\|	7087005 \|Intermittent (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1727509027) - 234422006 -> 7087005 (260908002) View
260908002 \|Course (attribute)\|	7087005 \|Intermittent (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2834642020) - 234422006 -> 418470004 (116680003) View
116680003 \|Is a (attribute)\|	418470004 \|Porphyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (514033028) - 234422006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (514032022) - 234422006 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (48090024) - 234422006 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (48091023) - 234422006 -> 276263005 (116680003) View
116680003 \|Is a (attribute)\|	276263005 \|Porphobilinogen deaminase deficiency (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
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
276263005 View
276263005	Porphobilinogen deaminase deficiency (disorder)	Pbgd deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
238054000 View
238054000	Homozygous acute intermittent porphyria (disorder)	Homozygous acute intermittent porphyria	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 (6e0c0f09-51da-5f53-96ad-3dd931655d5b) 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 234422006

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches