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Terminology chevron_right Concepts chevron_right 237938003

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Cobalamin g (disorder)

Shortest Term

Cobalamin g

Definition Status

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Cobalamin g (disorder)

SCTID: 237938003, Primitive, Active

237938003|Cobalamin g (disorder)|

Expression

237938003 |Cobalamin g (disorder)|
 <<< 360376008 |Functional defects of methionine synthase (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
356612015 - Cobalamin G (en) View
356612015	en	Synonym (core metadata concept)	Cobalamin G	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
626742015 - Cobalamin G (disorder) (en) View
626742015	en	Fully specified name (core metadata concept)	Cobalamin G (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
3029363016 - Deficiency of Cobalamin G (en) View
3029363016	en	Synonym (core metadata concept)	Deficiency of Cobalamin G	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3029318017 - Deficiency of Cobalamin G (disorder) (en) View
3029318017	en	Fully specified name (core metadata concept)	Deficiency of Cobalamin G (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (526910028) - 237938003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526911029) - 237938003 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53568023) - 237938003 -> 360376008 (116680003) View
116680003 \|Is a (attribute)\|	360376008 \|Functional defects of methionine synthase (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
360376008 View
360376008	Functional defects of methionine synthase (disorder)	Functional defects of methionine synthase	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 (70a80bdb-9dd4-53a8-bbc7-f8177076d0f6) 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)\|

Descriptions