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Terminology chevron_right Concepts chevron_right 61395005

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Component

61395005

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary persistence of fetal hemoglobin g gamma beta plus thalassemia (disorder)

Shortest Term

Hpfh g 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 g gamma beta plus thalassemia (disorder)

SCTID: 61395005, Primitive, Active

61395005|Hereditary persistence of fetal hemoglobin g gamma beta plus thalassemia (disorder)|

en Hereditary persistence of fetal haemoglobin g gamma beta plus thalassaemia
en Hereditary persistence of fetal hemoglobin g gamma beta plus thalassemia
en Hereditary persistence of fetal hemoglobin g gamma beta plus thalassemia (disorder)
en Hpfh (hereditary persistence of fetal haemoglobin) g gamma beta plus thalassaemia
en Hpfh (hereditary persistence of fetal hemoglobin) g gamma beta plus thalassemia
en Hpfh (hereditary persistence of foetal haemoglobin) g gamma beta plus thalassaemia

Expression

61395005 |Hereditary persistence of fetal hemoglobin g gamma beta plus 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
3793695017 - Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia (en) View
3793695017	en	Synonym (core metadata concept)	Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3793694018 - Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (en) View
3793694018	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3793698015 - Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder) (en) View
3793698015	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2914079019 - Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia (en) View
2914079019	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
2915152013 - Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia (disorder) (en) View
2915152013	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2620926017 - Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia (en) View
2620926017	en	Synonym (core metadata concept)	Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
2793196016 - Hereditary persistence of foetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia (en) View
2793196016	en	Synonym (core metadata concept)	Hereditary persistence of foetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
498999014 - HPFH G gamma beta^+^ thalassaemia (en) View
498999014	en	Synonym (core metadata concept)	HPFH G gamma beta^+^ thalassaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
102000014 - HPFH G gamma beta^+^ thalassemia (en) View
102000014	en	Synonym (core metadata concept)	HPFH G gamma beta^+^ thalassemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
3800043011 - HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia (en) View
3800043011	en	Synonym (core metadata concept)	HPFH (hereditary persistence of fetal haemoglobin) G gamma beta plus thalassaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3800044017 - HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia (en) View
3800044017	en	Synonym (core metadata concept)	HPFH (hereditary persistence of fetal hemoglobin) G gamma beta plus thalassemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3800045016 - HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia (en) View
3800045016	en	Synonym (core metadata concept)	HPFH (hereditary persistence of foetal haemoglobin) G gamma beta plus thalassaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2612458011 - Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia (disorder) (en) View
2612458011	en	Fully specified name (core metadata concept)	Hereditary persistence of fetal hemoglobin (HPFH) G gamma beta^+^ thalassemia (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2620925018 - Hereditary persistence of fetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia (en) View
2620925018	en	Synonym (core metadata concept)	Hereditary persistence of fetal haemoglobin (HPFH) G gamma beta^+^ thalassaemia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
800452017 - HPFH G gamma beta^+^ thalassemia (disorder) (en) View
800452017	en	Fully specified name (core metadata concept)	HPFH G gamma beta^+^ thalassemia (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6763991020) - 61395005 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763992029) - 61395005 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763994028) - 61395005 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13898398026) - 61395005 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (826901023) - 61395005 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006747024) - 61395005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006748025) - 61395005 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2268589024) - 61395005 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763993023) - 61395005 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3190677020) - 61395005 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268590026) - 61395005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (826902027) - 61395005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (247944025) - 61395005 -> 16964007 (116680003) View
116680003 \|Is a (attribute)\|	16964007 \|Hereditary persistence of fetal hemoglobin thalassemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (247945029) - 61395005 -> 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

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (d6008de9-d8aa-5a3c-942b-56681595625d) 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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