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Terminology chevron_right Concepts chevron_right 783766005

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783766005
The component that hold information about this concept.
Autosomal recessive secondary polycythemia not associated with von hippel lindau gene (disorder)
Autosomal recessive secondary polycythemia non-chuvash type
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

Autosomal recessive secondary polycythemia not associated with von hippel lindau gene (disorder)

SCTID: 783766005, Primitive, Active


783766005|Autosomal recessive secondary polycythemia not associated with von hippel lindau gene (disorder)|
  • en Autosomal recessive secondary erythrocytosis non-chuvash type
  • en Autosomal recessive secondary polycythaemia non-chuvash type
  • en Autosomal recessive secondary polycythaemia not associated with vhl (von hippel lindau) gene
  • en Autosomal recessive secondary polycythaemia not associated with von hippel lindau gene
  • en Autosomal recessive secondary polycythemia non-chuvash type
  • en Autosomal recessive secondary polycythemia not associated with vhl (von hippel lindau) gene
  • en Autosomal recessive secondary polycythemia not associated with von hippel lindau gene
  • en Autosomal recessive secondary polycythemia not associated with von hippel lindau gene (disorder)

783766005 |Autosomal recessive secondary polycythemia not associated with von hippel lindau gene (disorder)|

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

3760277019 - Autosomal recessive secondary erythrocytosis non-Chuvash type (en) View

3760277019
en
Synonym (core metadata concept)
Autosomal recessive secondary erythrocytosis non-Chuvash type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3760278012 - Autosomal recessive secondary polycythaemia non-Chuvash type (en) View

3760278012
en
Synonym (core metadata concept)
Autosomal recessive secondary polycythaemia non-Chuvash type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3760271018 - Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene (en) View

3760271018
en
Synonym (core metadata concept)
Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3760268014 - Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene (en) View

3760268014
en
Synonym (core metadata concept)
Autosomal recessive secondary polycythaemia not associated with Von Hippel Lindau gene
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3760276011 - Autosomal recessive secondary polycythemia non-Chuvash type (en) View

3760276011
en
Synonym (core metadata concept)
Autosomal recessive secondary polycythemia non-Chuvash type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3760272013 - Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene (en) View

3760272013
en
Synonym (core metadata concept)
Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3760270017 - Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (en) View

3760270017
en
Synonym (core metadata concept)
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3760269018 - Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder) (en) View

3760269018
en
Fully specified name (core metadata concept)
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (11323953028) - 783766005 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11323955024) - 783766005 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11323956020) - 783766005 -> 14089001 (363714003) View

363714003 |Interprets (attribute)|
14089001 |Red blood cell count (procedure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11323957027) - 783766005 -> 17342003 (116680003) View

116680003 |Is a (attribute)|
17342003 |Familial erythrocytosis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11323958021) - 783766005 -> 66091009 (116680003) View

116680003 |Is a (attribute)|
66091009 |Congenital disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11323959029) - 783766005 -> 41898006 (363698007) View

363698007 |Finding site (attribute)|
41898006 |Erythrocyte (cell)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11323960023) - 783766005 -> 281302008 (363713009) View

363713009 |Has interpretation (attribute)|
281302008 |Above reference range (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (11570819022) - 783766005 -> 33468001 (363714003) View

363714003 |Interprets (attribute)|
33468001 |Hematology procedure (procedure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

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

ExtendedMap object (648b1f97-d98d-58c5-8add-2fd7ca11c216) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D75.1
TRUE
ALWAYS D75.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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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