Myoclonic epilepsy
Symptom Information:
Symptom ID: | MedDRA:10054859 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Nervous system disorders(MedDRA:10029205) Seizures(HPO:0001250) Seizures and seizure disorders NEC(MedDRA:10039912) Myoclonic epilepsy(MedDRA:10054859) |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
MEGDEL syndrome | (Orphanet:352328) |
MENTAL RETARDATION, X-LINKED 89 | (OMIM:300848) |
MERRF | (Orphanet:551) |
MYOCLONIC EPILEPSY, HARTUNG TYPE | (OMIM:159600) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |