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Terminology chevron_right Concepts chevron_right 360376008

Production

Language with ID “56ff6e4e-48c5-5919-aa8a-bbebda8aacbf” doesn’t exist. Perhaps it was deleted?

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Functional defects of methionine synthase (disorder)

Shortest Term

Functional defects of methionine synthase

Definition Status

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

Summary

Functional defects of methionine synthase (disorder)

SCTID: 360376008, Primitive, Active

360376008|Functional defects of methionine synthase (disorder)|

Expression

360376008 |Functional defects of methionine synthase (disorder)|
 <<< 28882002 |Disorder of sulfur-bearing amino acid metabolism (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
476118018 - Functional defects of methionine synthase (en) View
476118018	en	Synonym (core metadata concept)	Functional defects of methionine synthase	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
740096014 - Functional defects of methionine synthase (disorder) (en) View
740096014	en	Fully specified name (core metadata concept)	Functional defects of methionine synthase (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (703224023) - 360376008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (703223028) - 360376008 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (168257023) - 360376008 -> 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
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
721225009 View
721225009	Homocystinuria without methylmalonic aciduria (disorder)	Functional methionine synthase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237937008 View
237937008	Cobalamin e (disorder)	Cobalamin e	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237938003 View
237938003	Cobalamin g (disorder)	Cobalamin g	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 (dac4d9cd-d3ef-549c-a71e-6405d64a88e9) 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