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Terminology chevron_right Concepts chevron_right 763349002

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763349002
The component that hold information about this concept.
Progressive myoclonic epilepsy with dystonia (disorder)
Progressive myoclonic epilepsy with dystonia
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

Progressive myoclonic epilepsy with dystonia (disorder)

SCTID: 763349002, Primitive, Active


763349002|Progressive myoclonic epilepsy with dystonia (disorder)|
  • en Progressive myoclonic epilepsy with dystonia
  • en Progressive myoclonic epilepsy with dystonia (disorder)
  • en Progressive myoclonus epilepsy with dystonia

763349002 |Progressive myoclonic epilepsy with dystonia (disorder)|

<<< 15802004 |Dystonia (disorder)| +
    85995004 |Autosomal recessive hereditary disorder (disorder)| +
    267581004 |Progressive myoclonic epilepsy (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)| }
Active

3638647011 - Progressive myoclonic epilepsy with dystonia (en) View

3638647011
en
Synonym (core metadata concept)
Progressive myoclonic epilepsy with dystonia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3638648018 - Progressive myoclonic epilepsy with dystonia (disorder) (en) View

3638648018
en
Fully specified name (core metadata concept)
Progressive myoclonic epilepsy with dystonia (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3638646019 - Progressive myoclonus epilepsy with dystonia (en) View

3638646019
en
Synonym (core metadata concept)
Progressive myoclonus epilepsy with dystonia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (13882854028) - 763349002 -> 255324009 (363714003) View

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

Relationship (16350682020) - 763349002 -> 363847004 (363714003) View

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

Relationship (9091961021) - 763349002 -> 15802004 (116680003) View

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

Relationship (13671789029) - 763349002 -> 439732004 (116680003) View

116680003 |Is a (attribute)|
439732004 |Myoclonic dystonia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9091965028) - 763349002 -> 76375004 (363698007) View

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

Relationship (9091966027) - 763349002 -> 83678007 (363698007) View

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

Relationship (9091962025) - 763349002 -> 85995004 (116680003) View

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

Relationship (9091963024) - 763349002 -> 267581004 (116680003) View

116680003 |Is a (attribute)|
267581004 |Progressive myoclonic epilepsy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9091964029) - 763349002 -> 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

85995004 View

85995004
Autosomal recessive hereditary disorder (disorder)
Hereditary disorder trait, nos
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

267581004 View

267581004
Progressive myoclonic epilepsy (disorder)
Progressive myoclonic epilepsy
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
esc