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Terminology chevron_right Concepts chevron_right 82286005

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Component

82286005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hyperimmunoglobulin m syndrome (disorder)

Shortest Term

Hyper igm syndrome

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

Hyperimmunoglobulin m syndrome (disorder)

SCTID: 82286005, Primitive, Active

82286005|Hyperimmunoglobulin m syndrome (disorder)|

en Hyper igm syndrome
en Immunodeficiency with igm hypergammaglobulinaemia
en Immunodeficiency with igm hypergammaglobulinemia
en Hyperimmunoglobulin m syndrome
en Hyperimmunoglobulin m syndrome (disorder)

Expression

82286005 |Hyperimmunoglobulin m syndrome (disorder)|
 <<< 58606001 |Primary immune deficiency disorder (disorder)|
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1234699010 - Hyper IgM syndrome (en) View
1234699010	en	Synonym (core metadata concept)	Hyper IgM syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
1216993016 - Immunodeficiency with IgM hypergammaglobulinaemia (en) View
1216993016	en	Synonym (core metadata concept)	Immunodeficiency with IgM hypergammaglobulinaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
1218484015 - Immunodeficiency with IgM hypergammaglobulinemia (en) View
1218484015	en	Synonym (core metadata concept)	Immunodeficiency with IgM hypergammaglobulinemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
136491010 - Hyperimmunoglobulin M syndrome (en) View
136491010	en	Synonym (core metadata concept)	Hyperimmunoglobulin M syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
823676012 - Hyperimmunoglobulin M syndrome (disorder) (en) View
823676012	en	Fully specified name (core metadata concept)	Hyperimmunoglobulin M syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (281729029) - 82286005 -> 58034007 (116680003) View
116680003 \|Is a (attribute)\|	58034007 \|Congenital hypergammaglobulinemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (879579028) - 82286005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16229481026) - 82286005 -> 58606001 (116680003) View
116680003 \|Is a (attribute)\|	58606001 \|Primary immune deficiency disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11172095029) - 82286005 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2738032027) - 82286005 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (879578020) - 82286005 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
58606001 View
58606001	Primary immune deficiency disorder (disorder)	Primary immunodeficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
403836001 View
403836001	Autosomal recessive hyper- immunoglobulin m syndrome (disorder)	Autosomal recessive hyper-igm syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
783248004 View
783248004	Hyperimmunoglobulin m syndrome with susceptibility to opportunistic infection (disorder)	Hyper-igm syndrome with susceptibility to opportunistic infections	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
783249007 View
783249007	Hyperimmunoglobulin m syndrome without susceptibility to opportunistic infection (disorder)	Hyper-igm syndrome without susceptibility to opportunistic infections	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 (4135d05a-5e9d-5229-9e75-c680734080e2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D80.5	TRUE	ALWAYS D80.5	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)\|

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