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Terminology chevron_right Concepts chevron_right 720466001

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720466001
The component that hold information about this concept.
Adult-onset dystonia parkinsonism (disorder)
Adult-onset dystonia parkinsonism
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

Adult-onset dystonia parkinsonism (disorder)

SCTID: 720466001, Defined, Active


720466001|Adult-onset dystonia parkinsonism (disorder)|
  • en Adult-onset dystonia parkinsonism
  • en Adult-onset dystonia parkinsonism (disorder)
  • en Dystonia parkinsonism paisan-ruiz type
  • en Pla2g6 (phospholipase a2 group vi) related dystonia parkinsonism

720466001 |Adult-onset dystonia parkinsonism (disorder)|

=== 15802004 |Dystonia (disorder)| +
    32798002 |Parkinsonism (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 246454002 |Occurrence (attribute)| = 41847000 |Adulthood (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 32610002 |Basal ganglion structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 255361000 |Slow (qualifier value)|,
          363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
Active

3320935018 - Adult-onset dystonia parkinsonism (en) View

3320935018
en
Synonym (core metadata concept)
Adult-onset dystonia parkinsonism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3320934019 - Adult-onset dystonia parkinsonism (disorder) (en) View

3320934019
en
Fully specified name (core metadata concept)
Adult-onset dystonia parkinsonism (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3320936017 - Dystonia parkinsonism Paisan-Ruiz type (en) View

3320936017
en
Synonym (core metadata concept)
Dystonia parkinsonism Paisan-Ruiz type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3320937014 - PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism (en) View

3320937014
en
Synonym (core metadata concept)
PLA2G6 (phospholipase A2 group VI) related dystonia parkinsonism
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (13882518024) - 720466001 -> 255324009 (363714003) View

363714003 |Interprets (attribute)|
255324009 |Movement (observable entity)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (13882519027) - 720466001 -> 255361000 (363713009) View

363713009 |Has interpretation (attribute)|
255361000 |Slow (qualifier value)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (16350835026) - 720466001 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16350836025) - 720466001 -> 255361000 (363713009) View

363713009 |Has interpretation (attribute)|
255361000 |Slow (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6683622025) - 720466001 -> 41847000 (246454002) View

246454002 |Occurrence (attribute)|
41847000 |Adulthood (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6683623024) - 720466001 -> 32610002 (363698007) View

363698007 |Finding site (attribute)|
32610002 |Basal ganglion structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6683618024) - 720466001 -> 15802004 (116680003) View

116680003 |Is a (attribute)|
15802004 |Dystonia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6683619027) - 720466001 -> 32798002 (116680003) View

116680003 |Is a (attribute)|
32798002 |Parkinsonism (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6683620022) - 720466001 -> 85995004 (116680003) View

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

Relationship (6683621021) - 720466001 -> 363235000 (116680003) View

116680003 |Is a (attribute)|
363235000 |Hereditary disorder of nervous system (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

15802004 View

15802004
Dystonia (disorder)
Dystonia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

32798002 View

32798002
Parkinsonism (disorder)
Parkinsonism
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

363235000 View

363235000
Hereditary disorder of nervous system (disorder)
Hereditary disorder of nervous system
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (e37416d0-3016-59e8-9e88-675577f1f00e) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G24.1
TRUE
ALWAYS G24.1 | 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)|
esc