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Terminology chevron_right Concepts chevron_right 702323008

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702323008
The component that hold information about this concept.
Rapid onset dystonia parkinsonism (disorder)
Dystonia 12
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

Rapid onset dystonia parkinsonism (disorder)

SCTID: 702323008, Primitive, Active


702323008|Rapid onset dystonia parkinsonism (disorder)|
  • en Dystonia 12
  • en Rapid onset dystonia parkinsonism
  • en Rapid onset dystonia parkinsonism (disorder)
  • en Dyt12 - dystonia 12

702323008 |Rapid onset dystonia parkinsonism (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    15802004 |Dystonia (disorder)| +
    32798002 |Parkinsonism (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 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

2995824011 - Dystonia 12 (en) View

2995824011
en
Synonym (core metadata concept)
Dystonia 12
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

2994982015 - Rapid onset dystonia parkinsonism (en) View

2994982015
en
Synonym (core metadata concept)
Rapid onset dystonia parkinsonism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2995754010 - Rapid onset dystonia parkinsonism (disorder) (en) View

2995754010
en
Fully specified name (core metadata concept)
Rapid onset dystonia parkinsonism (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

2995583010 - DYT12 - dystonia 12 (en) View

2995583010
en
Synonym (core metadata concept)
DYT12 - dystonia 12
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (13882568027) - 702323008 -> 255324009 (363714003) View

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

Relationship (13882569024) - 702323008 -> 255361000 (363713009) View

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

Relationship (16350666024) - 702323008 -> 363847004 (363714003) View

363714003 |Interprets (attribute)|
363847004 |Movement observable (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16350667026) - 702323008 -> 255361000 (363713009) View

363713009 |Has interpretation (attribute)|
255361000 |Slow (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (4967978023) - 702323008 -> 32610002 (363698007) View

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

Relationship (4967974020) - 702323008 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (4967975021) - 702323008 -> 15802004 (116680003) View

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

Relationship (4967976022) - 702323008 -> 32798002 (116680003) View

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

Relationship (4967977029) - 702323008 -> 363235000 (116680003) View

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

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (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

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 (7c4f313e-2f76-5b84-8061-774493bcaddb) 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)|
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