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Terminology chevron_right Concepts chevron_right 237933007

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Component

237933007

The component that hold information about this concept.

Fully Specified Name (FSN)

Transcobalamin i deficiency (disorder)

Shortest Term

R-binder deficiency

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

Transcobalamin i deficiency (disorder)

SCTID: 237933007, Primitive, Active

237933007|Transcobalamin i deficiency (disorder)|

en R-binder deficiency
en Transcobalamin i deficiency
en Transcobalamin i deficiency (disorder)

Expression

237933007 |Transcobalamin i deficiency (disorder)|
 <<< 28882002 |Disorder of sulfur-bearing amino acid metabolism (disorder)| + 
7521001 |Vitamin disease (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
356605012 - R-binder deficiency (en) View
356605012	en	Synonym (core metadata concept)	R-binder deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
356604011 - Transcobalamin I deficiency (en) View
356604011	en	Synonym (core metadata concept)	Transcobalamin I deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
626737011 - Transcobalamin I deficiency (disorder) (en) View
626737011	en	Fully specified name (core metadata concept)	Transcobalamin I deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (526905027) - 237933007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526904028) - 237933007 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53564020) - 237933007 -> 85670002 (116680003) View
116680003 \|Is a (attribute)\|	85670002 \|Vitamin deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1656722028) - 237933007 -> 7521001 (116680003) View
116680003 \|Is a (attribute)\|	7521001 \|Vitamin disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (53563025) - 237933007 -> 28882002 (116680003) View
116680003 \|Is a (attribute)\|	28882002 \|Disorder of sulfur-bearing amino acid metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
7521001 View
7521001	Vitamin disease (disorder)	Vitamin disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
28882002 View
28882002	Disorder of sulfur-bearing amino acid metabolism (disorder)	Sulfuraminoacidemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (de83cee4-0f68-5d57-a45d-218b2dc86bb9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E72.1	TRUE	ALWAYS E72.1	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 237933007

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