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Terminology chevron_right Concepts chevron_right 5967006

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Component

5967006

The component that hold information about this concept.

Fully Specified Name (FSN)

A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis (disorder)

Shortest Term

A>gamma< beta^+^ hpfh and beta^0^ thalassemia in cis

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

A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis (disorder)

SCTID: 5967006, Primitive, Active

5967006|A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis (disorder)|

en A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis
en A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis (disorder)
en A>gamma< beta^+^ hpfh and beta^0^ thalassaemia in cis
en A>gamma< beta^+^ hpfh and beta^0^ thalassemia in cis

Expression

5967006 |A gamma beta^+^ hereditary persistence of fetal hemoglobin and beta^0^ thalassemia in cis (disorder)|
 <<< 39586009 |Hereditary persistence of fetal hemoglobin a gamma beta^+^ 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
3023237017 - A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (en) View
3023237017	en	Synonym (core metadata concept)	A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
2968564010 - A>gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (en) View
2968564010	en	Synonym (core metadata concept)	A>gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
2988972011 - A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder) (en) View
2988972011	en	Fully specified name (core metadata concept)	A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
798538015 - A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis (disorder) (en) View
798538015	en	Fully specified name (core metadata concept)	A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
498509010 - A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis (en) View
498509010	en	Synonym (core metadata concept)	A>gamma< beta^+^ HPFH AND beta^0^ thalassaemia in cis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
10926015 - A>gamma< beta^+^ HPFH and beta^0^ thalassemia in cis (en) View
10926015	en	Synonym (core metadata concept)	A>gamma< beta^+^ HPFH and beta^0^ thalassemia in cis	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
10925016 - A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis (en) View
10925016	en	Synonym (core metadata concept)	A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6763412023) - 5967006 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763413029) - 5967006 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763415020) - 5967006 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13898426021) - 5967006 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (822444026) - 5967006 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7006566022) - 5967006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7006567029) - 5967006 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2268452023) - 5967006 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6763414024) - 5967006 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3190936023) - 5967006 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268453029) - 5967006 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (822443021) - 5967006 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (245156026) - 5967006 -> 39586009 (116680003) View
116680003 \|Is a (attribute)\|	39586009 \|Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
39586009 View
39586009	Hereditary persistence of fetal hemoglobin a gamma beta^+^ thalassemia (disorder)	Hpfh a gamma 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 (02301dad-ab39-53a7-ac48-c48a2ae156f4) 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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