ORPHA:1935
Early myoclonic encephalopathy
inactive · moved to ORPHA:1934Early infantile developmental and epileptic encephalopathy
Synonyms: Early myoclonic encephalopathy with suppression-bursts
- Type
- Clinical syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Early infantile epileptic encephalopathy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Early myoclonic encephalopathy | Early myoclonic encephalopathy with suppression-bursts |
| fr | Encéphalopathie myoclonique précoce | Encéphalopathie myoclonique précoce avec "suppression-bursts" |
| de | Enzephalopathie, frühkindliche myoklonische | Frühkindliche myoklonische Enzephalopathie mit Suppression-burst |
| es | Encefalopatía mioclónica temprana | |
| it | Encefalopatia mioclonica precoce | Encefalopatia mioclonica precoce con appiattimento elettrico cerebrale |
| nl | Vroege myoclonische encefalopathie | Vroege myoclonische encefalopathie met suppressie-uitbarstingen |
| pt | Encefalopatia mioclónica precoce | |
| pl | Wczesna encefalopatia miokloniczna | Wczesna encefalopatia miokloniczna z tłumieniem wyładowań |
| cs | Časná myoklonická encefalopatie | Časná myoklonická encefalopatie s periodickými výboji s následujícím útlumem na EEG |
| uk | Рання міоклонічна енцефалопатія | Рання міоклонічна енцефалопатія з судомними нападами |
| zh | 早期肌阵挛性脑病 | 早期肌阵挛脑病伴抑制-爆发 |
| tr | Erken miyoklonik ensefalopati | Supresyon patlamaları ile seyreden erken miyoklonik ensefalopati |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016022 | E | validated | |
| UMLS | C0270855 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1935
- This record as JSON: /data/d/1935.json