dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 40108008

Production

add

Component

40108008

The component that hold information about this concept.

Fully Specified Name (FSN)

Thalassemia (disorder)

Shortest Term

Thalassemia

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

Thalassemia (disorder)

SCTID: 40108008, Primitive, Active

40108008|Thalassemia (disorder)|

vi Bệnh thalassemia
en Hereditary leptocytosis
en Thalassaemia
en Thalassemia
en Thalassemia (disorder)

Expression

40108008 |Thalassemia (disorder)|
 <<< 14514008 |Anemia due to disturbance of hemoglobin synthesis (disorder)| + 
427306008 |Hereditary hemoglobinopathy (disorder)|
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
567631000003118 - bệnh Thalassemia (vi) View
567631000003118	vi	Synonym (core metadata concept)	bệnh Thalassemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
1229603011 - Hereditary leptocytosis (en) View
1229603011	en	Synonym (core metadata concept)	Hereditary leptocytosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
492446019 - Thalassaemia (en) View
492446019	en	Synonym (core metadata concept)	Thalassaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
66816015 - Thalassemia (en) View
66816015	en	Synonym (core metadata concept)	Thalassemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
776688019 - Thalassemia (disorder) (en) View
776688019	en	Fully specified name (core metadata concept)	Thalassemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
66817012 - Thalassemia, NOS (en) View
66817012	en	Synonym (core metadata concept)	Thalassemia, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6763779020) - 40108008 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763780023) - 40108008 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763782026) - 40108008 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9464311028) - 40108008 -> 63565007 (116680003) View
116680003 \|Is a (attribute)\|	63565007 \|Congenital anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13898415026) - 40108008 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (772133028) - 40108008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006685026) - 40108008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006686025) - 40108008 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2266732026) - 40108008 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763781022) - 40108008 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3190857027) - 40108008 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (213376023) - 40108008 -> 80141007 (116680003) View
116680003 \|Is a (attribute)\|	80141007 \|Hemoglobinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2691774021) - 40108008 -> 32895009 (116680003) View
116680003 \|Is a (attribute)\|	32895009 \|Hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3171666025) - 40108008 -> 427306008 (116680003) View
116680003 \|Is a (attribute)\|	427306008 \|Hereditary hemoglobinopathy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (213377025) - 40108008 -> 363136009 (116680003) View
116680003 \|Is a (attribute)\|	363136009 \|Hereditary disorder of hematologic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2266733020) - 40108008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (772134023) - 40108008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (213375022) - 40108008 -> 14514008 (116680003) View
116680003 \|Is a (attribute)\|	14514008 \|Anemia due to disturbance of hemoglobin synthesis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
427306008 View
427306008	Hereditary hemoglobinopathy (disorder)	Hereditary hemoglobinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
14514008 View
14514008	Anemia due to disturbance of hemoglobin synthesis (disorder)	Anemia due to disturbance of hemoglobin synthesis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
72331000119105 View
72331000119105	Thalassemia in mother complicating pregnancy (disorder)	Maternal thalassemia in pregnancy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
10806241000119108 View
10806241000119108	Thalassemia in mother complicating childbirth (disorder)	Maternal thalassemia in childbirth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
934007 View
934007	Thalassemia intermedia (disorder)	Thalassemia intermedia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
16427007 View
16427007	Delta thalassemia (disorder)	Delta thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
16964007 View
16964007	Hereditary persistence of fetal hemoglobin thalassemia (disorder)	Hpfh	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
19442009 View
19442009	Heterozygous thalassemia (disorder)	Thalassemia minor	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
47047009 View
47047009	Thalassemia with other hemoglobinopathy (disorder)	Thalassemia with other hemoglobinopathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
65959000 View
65959000	Beta thalassemia (disorder)	Beta thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
68913001 View
68913001	Alpha thalassemia (disorder)	Alpha thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
69216008 View
69216008	Hb lepore thalassemia (disorder)	Hb lepore thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
75451007 View
75451007	Thalassemia major (disorder)	Thalassemia major	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
84188003 View
84188003	Thalassemia syndrome (disorder)	Thalassemia syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234389001 View
234389001	Alpha-beta thalassemia (disorder)	Alpha-beta thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234390005 View
234390005	Gamma thalassemia (disorder)	Gamma thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
307343001 View
307343001	Acquired hemoglobin h disease (disorder)	Acquired hemoglobin h disease	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 (a0b70ffb-0908-5db7-800a-0c0d7543d938) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D56.9	TRUE	ALWAYS D56.9	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)\|

Terminology chevron_right Concepts chevron_right 40108008

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches