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Terminology chevron_right Concepts chevron_right 39586009

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Component

39586009

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)

Shortest Term

Hpfh a gamma beta^+^ 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

Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)

SCTID: 39586009, Primitive, Active

39586009|Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)|

en Hereditary persistence of fetal haemoglobin a gamma beta^+^ thalassaemia
en Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia
en Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)
en Hereditary persistence of foetal haemoglobin (hpfh) a gamma beta^+^ thalassaemia
en Hereditary persistence of fetal hemoglobin (hpfh) a gamma beta^+^ thalassemia
en Hpfh a gamma beta^+^ thalassaemia
en Hpfh a gamma beta^+^ thalassemia

Expression

39586009 |Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)|
 <<< 16964007 |Hereditary persistence of fetal hemoglobin thalassemia (disorder)| + 
79592006 |Beta plus thalassemia (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
3012701016 - Hereditary persistence of fetal haemoglobin A gamma beta^+^ thalassaemia (en) View
3012701016	en	Synonym (core metadata concept)	Hereditary persistence of fetal haemoglobin A gamma beta^+^ thalassaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2914263013 - Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (en) View
2914263013	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2914230018 - Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) (en) View
2914230018	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2612287014 - Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia (disorder) (en) View
2612287014	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2620663012 - Hereditary persistence of fetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia (en) View
2620663012	en	Synonym (core metadata concept)	Hereditary persistence of fetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
2793326018 - Hereditary persistence of foetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia (en) View
2793326018	en	Synonym (core metadata concept)	Hereditary persistence of foetal haemoglobin (HPFH) A gamma beta^+^ thalassaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2620662019 - Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia (en) View
2620662019	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin (HPFH) A gamma beta^+^ thalassemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
776066018 - HPFH A gamma beta^+^ thalassemia (disorder) (en) View
776066018	en	Fully specified name (core metadata concept)	HPFH A gamma beta^+^ thalassemia (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
492143018 - HPFH A gamma beta^+^ thalassaemia (en) View
492143018	en	Synonym (core metadata concept)	HPFH A gamma beta^+^ thalassaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
66390015 - HPFH A gamma beta^+^ thalassemia (en) View
66390015	en	Synonym (core metadata concept)	HPFH A gamma beta^+^ thalassemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6763775025) - 39586009 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763776029) - 39586009 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763778028) - 39586009 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13898413022) - 39586009 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (770744024) - 39586009 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006680020) - 39586009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006681024) - 39586009 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2266693026) - 39586009 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763777022) - 39586009 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3190684028) - 39586009 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2266694021) - 39586009 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (770745020) - 39586009 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (212457027) - 39586009 -> 16964007 (116680003) View
116680003 \|Is a (attribute)\|	16964007 \|Hereditary persistence of fetal hemoglobin thalassemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (212458021) - 39586009 -> 79592006 (116680003) View
116680003 \|Is a (attribute)\|	79592006 \|Beta plus thalassemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
16964007 View
16964007	Hereditary persistence of fetal hemoglobin thalassemia (disorder)	Hpfh	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
79592006 View
79592006	Beta plus thalassemia (disorder)	Beta + thalassemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
5967006 View
5967006	A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis (disorder)	A>gamma< beta^+^ hpfh and beta^0^ thalassemia in cis	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 (b5b8d821-8baf-5e3c-998e-e658a7873078) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D56.4	TRUE	ALWAYS D56.4	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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