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Terminology chevron_right Concepts chevron_right 58648008

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Component

58648008

The component that hold information about this concept.

Fully Specified Name (FSN)

Benign monoclonal gammopathy (disorder)

Shortest Term

Benign monoclonal gammopathy

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

Benign monoclonal gammopathy (disorder)

SCTID: 58648008, Primitive, Active

58648008|Benign monoclonal gammopathy (disorder)|

vi Bệnh gammopathy đơn dòng lành tính
en Asymptomatic monoclonal gammopathy
en Benign monoclonal gammopathy
en Benign monoclonal gammopathy (disorder)

Expression

58648008 |Benign monoclonal gammopathy (disorder)|
 <<< 109983007 |Monoclonal gammopathy (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 270994009 |Serum globulin measurement (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 260373001 |Detected (qualifier value)|,
363714003 |Interprets (attribute)| = 250174000 |Paraprotein measurement (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 42441008 |Immunoglobulin measurement (procedure)| }
        { 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
484091000003112 - bệnh gammopathy đơn dòng lành tính (vi) View
484091000003112	vi	Synonym (core metadata concept)	bệnh gammopathy đơn dòng lành tính	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
97457015 - Asymptomatic monoclonal gammopathy (en) View
97457015	en	Synonym (core metadata concept)	Asymptomatic monoclonal gammopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
97456012 - Benign monoclonal gammopathy (en) View
97456012	en	Synonym (core metadata concept)	Benign monoclonal gammopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
797403017 - Benign monoclonal gammopathy (disorder) (en) View
797403017	en	Fully specified name (core metadata concept)	Benign monoclonal gammopathy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9478355028) - 58648008 -> 52101004 (363713009) View
363713009 \|Has interpretation (attribute)\|	52101004 \|Present (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15619903021) - 58648008 -> 260373001 (363713009) View
363713009 \|Has interpretation (attribute)\|	260373001 \|Detected (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11170442027) - 58648008 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2734813027) - 58648008 -> 414763006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	414763006 \|Monoclonal band present (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3592981020) - 58648008 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3592982029) - 58648008 -> 131136006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	131136006 \|Immunoglobulin above reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9478352025) - 58648008 -> 42441008 (363714003) View
363714003 \|Interprets (attribute)\|	42441008 \|Immunoglobulin measurement (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9478353024) - 58648008 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9478354029) - 58648008 -> 250174000 (363714003) View
363714003 \|Interprets (attribute)\|	250174000 \|Paraprotein measurement (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2734814022) - 58648008 -> 166787006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	166787006 \|Serum gamma globulin above reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7599860026) - 58648008 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7599861027) - 58648008 -> 270994009 (363714003) View
363714003 \|Interprets (attribute)\|	270994009 \|Serum globulin measurement (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (819403027) - 58648008 -> 35601003 (116676008) View
116676008 \|Associated morphology (attribute)\|	35601003 \|Monoclonal gammopathy of undetermined significance (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (819404022) - 58648008 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (819406024) - 58648008 -> 52501007 (363698007) View
363698007 \|Finding site (attribute)\|	52501007 \|Leukocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (819405023) - 58648008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (243471022) - 58648008 -> 109983007 (116680003) View
116680003 \|Is a (attribute)\|	109983007 \|Monoclonal gammopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
109983007 View
109983007	Monoclonal gammopathy (disorder)	Monoclonal gammopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
395692003 View
395692003	Benign paraproteinemia (disorder)	Benign paraproteinemia	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 (10062945-4469-5a4e-924f-3ffc8a06d7f0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (9bab6752-863c-566b-a11e-b8a6bbfc48fb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D47.2	TRUE	ALWAYS D47.2 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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)\|
ExtendedMap object (eea1a3ff-392a-52aa-bc0b-96e605282073) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D89.2	IFA 395692003 \| Benign paraproteinemia (disorder) \|	IF BENIGN PARAPROTEINEMIA CHOOSE D89.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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