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Terminology chevron_right Concepts chevron_right 74653006

Production

Component

The component that hold information about this concept.

Fully Specified Name (FSN)

Cobalamin c disease (disorder)

Shortest Term

Cobalamin c disease

Definition Status

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

Summary

Cobalamin c disease (disorder)

SCTID: 74653006, Primitive, Active

74653006|Cobalamin c disease (disorder)|

Expression

74653006 |Cobalamin c disease (disorder)|
 <<< 4409006 |Adenosylcobalamin and methylcobalamin synthesis defect (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1233774014 - CblC - Cobalamin locus C (en) View
1233774014	en	Synonym (core metadata concept)	CblC - Cobalamin locus C	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1216917016 - CblC methylmalonic acidaemia and homocystinuria (en) View
1216917016	en	Synonym (core metadata concept)	CblC methylmalonic acidaemia and homocystinuria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1218404017 - CblC methylmalonic acidemia and homocystinuria (en) View
1218404017	en	Synonym (core metadata concept)	CblC methylmalonic acidemia and homocystinuria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1233773015 - Cobalamin locus C variant (en) View
1233773015	en	Synonym (core metadata concept)	Cobalamin locus C variant	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
123975018 - Cobalamin C disease (en) View
123975018	en	Synonym (core metadata concept)	Cobalamin C disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
815176014 - Cobalamin C disease (disorder) (en) View
815176014	en	Fully specified name (core metadata concept)	Cobalamin C disease (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (860399026) - 74653006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (860398023) - 74653006 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (269401023) - 74653006 -> 4409006 (116680003) View
116680003 \|Is a (attribute)\|	4409006 \|Adenosylcobalamin and methylcobalamin synthesis defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
4409006 View
4409006	Adenosylcobalamin and methylcobalamin synthesis defect (disorder)	Adenosylcobalamin and methylcobalamin synthesis defect	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 (5eaf6fc9-d87b-5f15-84a0-b9931d53251e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E71.1	TRUE	ALWAYS E71.1	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