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Terminology chevron_right Concepts chevron_right 18273004

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Component

18273004

The component that hold information about this concept.

Fully Specified Name (FSN)

Unstable hemoglobin disease (disorder)

Shortest Term

Unstable hemoglobin disease

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

Unstable hemoglobin disease (disorder)

SCTID: 18273004, Primitive, Active

18273004|Unstable hemoglobin disease (disorder)|

en Unstable haemoglobin disease
en Unstable hemoglobin disease
en Unstable hemoglobin disease (disorder)
en Chbha - congenital heinz body hemolytic anemia
en Chbha - congenital heinz body haemolytic anaemia
en Congenital heinz body anaemia
en Congenital heinz body anemia
en Congenital heinz body haemolytic anaemia
en Congenital heinz body hemolytic anemia

Expression

18273004 |Unstable hemoglobin disease (disorder)|
 <<< 127038008 |Hereditary hemoglobinopathy due to globin chain mutation (disorder)| + 
63565007 |Congenital anemia (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)| = 14089001 |Red blood cell count (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
478537013 - Unstable haemoglobin disease (en) View
478537013	en	Synonym (core metadata concept)	Unstable haemoglobin disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
30860015 - Unstable hemoglobin disease (en) View
30860015	en	Synonym (core metadata concept)	Unstable hemoglobin disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
745671014 - Unstable hemoglobin disease (disorder) (en) View
745671014	en	Fully specified name (core metadata concept)	Unstable hemoglobin disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
478538015 - CHBHA - Congenital Heinz body hemolytic anemia (en) View
478538015	en	Synonym (core metadata concept)	CHBHA - Congenital Heinz body hemolytic anemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
478540013 - CHBHA - Congenital Heinz body haemolytic anaemia (en) View
478540013	en	Synonym (core metadata concept)	CHBHA - Congenital Heinz body haemolytic anaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
478536016 - Congenital Heinz body anaemia (en) View
478536016	en	Synonym (core metadata concept)	Congenital Heinz body anaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
30862011 - Congenital Heinz body anemia (en) View
30862011	en	Synonym (core metadata concept)	Congenital Heinz body anemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
478541012 - Congenital Heinz body haemolytic anaemia (en) View
478541012	en	Synonym (core metadata concept)	Congenital Heinz body haemolytic anaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
478539011 - Congenital Heinz body hemolytic anemia (en) View
478539011	en	Synonym (core metadata concept)	Congenital Heinz body hemolytic anemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
30861016 - Unstable hemoglobin disease, NOS (en) View
30861016	en	Synonym (core metadata concept)	Unstable hemoglobin disease, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2264775024) - 18273004 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9336851027) - 18273004 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9336852023) - 18273004 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9340745023) - 18273004 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9340746024) - 18273004 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (715856029) - 18273004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715857022) - 18273004 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006602025) - 18273004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006603024) - 18273004 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5971429020) - 18273004 -> 271737000 (116680003) View
116680003 \|Is a (attribute)\|	271737000 \|Anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2729405026) - 18273004 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264776020) - 18273004 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715858028) - 18273004 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (176085024) - 18273004 -> 127038008 (116680003) View
116680003 \|Is a (attribute)\|	127038008 \|Hereditary hemoglobinopathy due to globin chain mutation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (176086020) - 18273004 -> 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
63565007 View
63565007	Congenital anemia (disorder)	Congenital anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
127038008 View
127038008	Hereditary hemoglobinopathy due to globin chain mutation (disorder)	Structural hemoglobinopathy	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 (b1055725-7d46-5784-b33e-ec46063bf361) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D58.2	TRUE	ALWAYS D58.2	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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