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Terminology chevron_right Concepts chevron_right 1231737000

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1231737000
The component that hold information about this concept.
Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)
Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome
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

Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)

SCTID: 1231737000, Primitive, Active


1231737000|Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)|
  • en Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome
  • en Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)

1231737000 |Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)|

<<< 230310003 |Paroxysmal dystonia (disorder)| +
    44145005 |Benign rolandic epilepsy (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    363235000 |Hereditary disorder of nervous system (disorder)| :
        { 363698007 |Finding site (attribute)| = 76375004 |Extrapyramidal system structure (body structure)| }
        { 363698007 |Finding site (attribute)| = 83678007 |Cerebral structure (body structure)| }
        { 363714003 |Interprets (attribute)| = 363847004 |Movement observable (observable entity)| }
        { 263502005 |Clinical course (attribute)| = 26593000 |Paroxysmal (qualifier value)| }
Active

5074088017 - Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (en) View

5074088017
en
Synonym (core metadata concept)
Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

5074073010 - Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder) (en) View

5074073010
en
Fully specified name (core metadata concept)
Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (15244737024) - 1231737000 -> 255324009 (363714003) View

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

Relationship (16350947022) - 1231737000 -> 363847004 (363714003) View

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

Relationship (15244734028) - 1231737000 -> 363235000 (116680003) View

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

Relationship (15244735027) - 1231737000 -> 44145005 (116680003) View

116680003 |Is a (attribute)|
44145005 |Benign rolandic epilepsy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15244736026) - 1231737000 -> 85995004 (116680003) View

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

Relationship (15244738025) - 1231737000 -> 76375004 (363698007) View

363698007 |Finding site (attribute)|
76375004 |Extrapyramidal system structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15244739022) - 1231737000 -> 83678007 (363698007) View

363698007 |Finding site (attribute)|
83678007 |Cerebral structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15244757023) - 1231737000 -> 230310003 (116680003) View

116680003 |Is a (attribute)|
230310003 |Paroxysmal dystonia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (15244758029) - 1231737000 -> 26593000 (263502005) View

263502005 |Clinical course (attribute)|
26593000 |Paroxysmal (qualifier value)|
4
900000000000011006 |Inferred relationship (core metadata concept)|
True

44145005 View

44145005
Benign rolandic epilepsy (disorder)
Centralopathic epilepsy
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

230310003 View

230310003
Paroxysmal dystonia (disorder)
Paroxysmal dystonia
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 (2a866ddb-52e5-55c7-8926-f9e4d9673b0a) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
G40.4
TRUE
ALWAYS G40.4 | 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