OMOP Concept 37204409
Progressive myoclonic epilepsy type 3
StandardConditionSNOMED783064000Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Progressive myoclonic epilepsy type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567095 | Epilepsy, Progressive Myoclonic 3 | Non-standard |
Synonyms
Alternative names recorded for Progressive myoclonic epilepsy type 3 across source vocabularies.
- epilepsia mioclónica progresiva tipo 3
- epilepsia mioclónica progresiva tipo 3 (trastorno)
- PME (progressive myoclonic epilepsy) type 3
- Progressive myoclonic epilepsy due to KCTD7 deficiency
- Progressive myoclonic epilepsy type 3 (disorder)
- Progressive myoclonus epilepsy type 3
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(46)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cerebral degeneration
- 1Chronic brain syndrome
- 1Chronic metabolic disorder
- 1Hereditary degenerative disease of central nervous system
- 1Infantile neuronal ceroid lipofuscinosis
- 1Progressive myoclonic epilepsy
- 2Autosomal hereditary disorder
- 2Chronic disease
- 2Chronic nervous system disorder
- 2Degenerative brain disorder
- 2Degenerative disease of the central nervous system
- 2Disorder of brain
- 2Epilepsy
- 2Hereditary disorder of nervous system
- 2Metabolic disease
- 2Neuronal ceroid lipofuscinosis
- 3Degenerative disorder
- 3Disease
- 3Disorder of head
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Finding of brain
- 3Hereditary disease
- 3Hereditary disorder by system
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