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Terminology chevron_right Concepts chevron_right 770407006

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Component

770407006

The component that hold information about this concept.

Fully Specified Name (FSN)

Chuvash erythrocytosis (disorder)

Shortest Term

Chuvash polycythemia

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

Chuvash erythrocytosis (disorder)

SCTID: 770407006, Primitive, Active

770407006|Chuvash erythrocytosis (disorder)|

en Chuvash erythrocytosis
en Chuvash erythrocytosis (disorder)
en Chuvash polycythaemia
en Chuvash polycythemia
en Von hippel lindau dependent polycythaemia
en Von hippel lindau dependent polycythemia

Expression

770407006 |Chuvash erythrocytosis (disorder)|
 <<< 17342003 |Familial erythrocytosis (disorder)| + 
66091009 |Congenital disease (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 14089001 |Red blood cell count (procedure)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363714003 |Interprets (attribute)| = 33468001 |Hematology procedure (procedure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3700723013 - Chuvash erythrocytosis (en) View
3700723013	en	Synonym (core metadata concept)	Chuvash erythrocytosis	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3700726017 - Chuvash erythrocytosis (disorder) (en) View
3700726017	en	Fully specified name (core metadata concept)	Chuvash erythrocytosis (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3700722015 - Chuvash polycythaemia (en) View
3700722015	en	Synonym (core metadata concept)	Chuvash polycythaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3700721010 - Chuvash polycythemia (en) View
3700721010	en	Synonym (core metadata concept)	Chuvash polycythemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3700724019 - Von Hippel Lindau dependent polycythaemia (en) View
3700724019	en	Synonym (core metadata concept)	Von Hippel Lindau dependent polycythaemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
3700725018 - Von Hippel Lindau dependent polycythemia (en) View
3700725018	en	Synonym (core metadata concept)	Von Hippel Lindau dependent polycythemia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9619372022) - 770407006 -> 33468001 (363714003) View
363714003 \|Interprets (attribute)\|	33468001 \|Hematology procedure (procedure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619373028) - 770407006 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619376020) - 770407006 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619378021) - 770407006 -> 17342003 (116680003) View
116680003 \|Is a (attribute)\|	17342003 \|Familial erythrocytosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9625275027) - 770407006 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9625276026) - 770407006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9625277024) - 770407006 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9625278025) - 770407006 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
17342003 View
17342003	Familial erythrocytosis (disorder)	Familial polycythemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	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 (23df94ea-8c1c-5e00-9ef2-92af9772736a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D75.1	TRUE	ALWAYS D75.1	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)\|
ExtendedMap object (455c2b1a-6276-5741-94c6-7918a07baac2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D75.0	TRUE	ALWAYS D75.0	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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