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Terminology chevron_right Concepts chevron_right 42601008

Production

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Component

42601008

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital hemolytic anemia (disorder)

Shortest Term

Congenital hemolytic anemia

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

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

Summary

Congenital hemolytic anemia (disorder)

SCTID: 42601008, Defined, Active

42601008|Congenital hemolytic anemia (disorder)|

en Congenital haemolytic anaemia
en Congenital hemolytic anemia
en Congenital hemolytic anemia (disorder)

Expression

42601008 |Congenital hemolytic anemia (disorder)|
 === 63565007 |Congenital anemia (disorder)| + 
61261009 |Hemolytic anemia (disorder)| + 
38292009 |Red blood cell disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 14089001 |Red blood cell count (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 52101004 |Present (qualifier value)|,
363714003 |Interprets (attribute)| = 404227002 |Hemolysis (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
493386016 - Congenital haemolytic anaemia (en) View
493386016	en	Synonym (core metadata concept)	Congenital haemolytic anaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
71069015 - Congenital hemolytic anemia (en) View
71069015	en	Synonym (core metadata concept)	Congenital hemolytic anemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
779519013 - Congenital hemolytic anemia (disorder) (en) View
779519013	en	Fully specified name (core metadata concept)	Congenital hemolytic anemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
71070019 - Congenital hemolytic anemia, NOS (en) View
71070019	en	Synonym (core metadata concept)	Congenital hemolytic anemia, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6763813021) - 42601008 -> 128086004 (116680003) View
116680003 \|Is a (attribute)\|	128086004 \|Hemolytic disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15069131021) - 42601008 -> 38292009 (116680003) View
116680003 \|Is a (attribute)\|	38292009 \|Red blood cell disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9214431025) - 42601008 -> 84054007 (363714003) View
363714003 \|Interprets (attribute)\|	84054007 \|Erythrocyte destruction, function (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11105095029) - 42601008 -> 52101004 (363713009) View
363713009 \|Has interpretation (attribute)\|	52101004 \|Present (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11105096028) - 42601008 -> 404227002 (363714003) View
363714003 \|Interprets (attribute)\|	404227002 \|Hemolysis (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (217487029) - 42601008 -> 61261009 (116680003) View
116680003 \|Is a (attribute)\|	61261009 \|Hemolytic anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2266953026) - 42601008 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2732705021) - 42601008 -> 73320003 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	73320003 \|Hemolysis (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9214432021) - 42601008 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9214434022) - 42601008 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9238393028) - 42601008 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9238394023) - 42601008 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (778581024) - 42601008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (778582028) - 42601008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2266952020) - 42601008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (778580020) - 42601008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (217486022) - 42601008 -> 63565007 (116680003) View
116680003 \|Is a (attribute)\|	63565007 \|Congenital anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
38292009 View
38292009	Red blood cell disorder (disorder)	Red blood cell disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
61261009 View
61261009	Hemolytic anemia (disorder)	Hemolytic anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
63565007 View
63565007	Congenital anemia (disorder)	Congenital anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
191169008 View
191169008	Hereditary elliptocytosis (disorder)	Hereditary ovalocytosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363041004 View
363041004	Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder)	Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism	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 (fc4c49d6-3cd4-53ce-863e-5227a7ec9efb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D58.9	TRUE	ALWAYS D58.9	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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