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Terminology chevron_right Concepts chevron_right 127036007

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Component

127036007

The component that hold information about this concept.

Fully Specified Name (FSN)

Cytochrome b>3< deficiency (disorder)

Shortest Term

Cytochrome b>3< 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

Cytochrome b>3< deficiency (disorder)

SCTID: 127036007, Primitive, Inactive

127036007|Cytochrome b>3< deficiency (disorder)|

en Cytochrome b>3< deficiency
en Cytochrome b>3< deficiency (disorder)

Expression

127036007 |Cytochrome b>3< deficiency (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
324011 - Cytochrome b>3< deficiency (en) View
324011	en	Synonym (core metadata concept)	Cytochrome b>3< deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
731074014 - Cytochrome b>3< deficiency (disorder) (en) View
731074014	en	Fully specified name (core metadata concept)	Cytochrome b>3< deficiency (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (161629025) - 127036007 -> 237987001 (116680003) View
116680003 \|Is a (attribute)\|	237987001 \|Deficiency in enzyme complexes of mitochondrial respiratory chain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (161630024) - 127036007 -> 123768009 (116680003) View
116680003 \|Is a (attribute)\|	123768009 \|Hereditary methemoglobinemia, enzymatic type (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694735023) - 127036007 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694736024) - 127036007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2728257023) - 127036007 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264017028) - 127036007 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694734022) - 127036007 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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

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 (b960d5ed-7632-5418-b80b-eeb94351c801) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E88.0	TRUE	ALWAYS E88.0	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)\|

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (161629025) - 127036007 -> 237987001 (116680003) View
116680003 \|Is a (attribute)\|	237987001 \|Deficiency in enzyme complexes of mitochondrial respiratory chain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (161630024) - 127036007 -> 123768009 (116680003) View
116680003 \|Is a (attribute)\|	123768009 \|Hereditary methemoglobinemia, enzymatic type (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694735023) - 127036007 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694736024) - 127036007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2728257023) - 127036007 -> 250228007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250228007 \|Red blood cell finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264017028) - 127036007 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (694734022) - 127036007 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

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