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Terminology chevron_right Concepts chevron_right 722966004

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722966004
The component that hold information about this concept.
Chorea due to heredodegenerative disorder (disorder)
Chorea due to heredodegenerative disorder
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Chorea due to heredodegenerative disorder (disorder)

SCTID: 722966004, Defined, Active


722966004|Chorea due to heredodegenerative disorder (disorder)|
  • en Chorea due to heredodegenerative disorder
  • en Chorea due to heredodegenerative disorder (disorder)

722966004 |Chorea due to heredodegenerative disorder (disorder)|

=== 271700006 |Chorea (disorder)| +
    87536007 |Central nervous system complication (disorder)| :
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 42752001 |Due to (attribute)| = 106018006 |Hereditary degenerative disease of central nervous system (disorder)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

3334048018 - Chorea due to heredodegenerative disorder (en) View

3334048018
en
Synonym (core metadata concept)
Chorea due to heredodegenerative disorder
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3334212013 - Chorea due to heredodegenerative disorder (disorder) (en) View

3334212013
en
Fully specified name (core metadata concept)
Chorea due to heredodegenerative disorder (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (12091631027) - 722966004 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6795855023) - 722966004 -> 230298007 (116680003) View

116680003 |Is a (attribute)|
230298007 |Disorder presenting primarily with chorea (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6795857026) - 722966004 -> 25087005 (363698007) View

363698007 |Finding site (attribute)|
25087005 |Structure of nervous system (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (13882875020) - 722966004 -> 60342002 (116680003) View

116680003 |Is a (attribute)|
60342002 |Movement disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15503898021) - 722966004 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15503899029) - 722966004 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15508644021) - 722966004 -> 87536007 (116680003) View

116680003 |Is a (attribute)|
87536007 |Central nervous system complication (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15508645022) - 722966004 -> 32610002 (363698007) View

363698007 |Finding site (attribute)|
32610002 |Basal ganglion structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6795854022) - 722966004 -> 106018006 (42752001) View

42752001 |Due to (attribute)|
106018006 |Hereditary degenerative disease of central nervous system (disorder)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6795856024) - 722966004 -> 271700006 (116680003) View

116680003 |Is a (attribute)|
271700006 |Chorea (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

87536007 View

87536007
Central nervous system complication (disorder)
Central nervous system complication
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

271700006 View

271700006
Chorea (disorder)
Chorea
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

724766009 View

724766009
Chorea co-occurrent and due to wilson disease (disorder)
Chorea with wilson disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

1259611004 View

1259611004
Chorea due to classical pantothenate kinase associated neurodegeneration (disorder)
Chorea due to classical pigmentary pallidal degeneration
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

1259689006 View

1259689006
Chorea due to huntington disease-like 2 (disorder)
Chorea due to huntington disease-like 2
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

1259694006 View

1259694006
Chorea due to huntington disease-like 1 (disorder)
Chorea due to huntington disease-like 1
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (a39f6c63-4e23-5125-922e-86c6e9414e42) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G10
TRUE
ALWAYS G10
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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