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| Term | progressive myoclonus epilepsy | ID (Ontology) | DOID:891 (Human Disease) |
| Definition | A variable age at onset electroclinical syndrome characterized by a relentlessly progressive disease course until death. | ||
| Also Known As | "PME" ; "progressive myoclonic epilepsy" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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electroclinical syndrome |__variable age at onset electroclinical syndrome |__progressive myoclonus epilepsy 19 rec. |__Lafora disease 4 rec. |__progressive myoclonus epilepsy 3 |__progressive myoclonus epilepsy 4 3 rec. |__progressive myoclonus epilepsy 6 2 rec. |__progressive myoclonus epilepsy 7 1 rec. |__progressive myoclonus epilepsy 8 |__progressive myoclonus epilepsy 9 2 rec. |__progressive myoclonus epilepsy 10 1 rec. |__Unverricht-Lundborg syndrome 3 rec. |__progressive myoclonus epilepsy 1A |__progressive myoclonus epilepsy 1B 3 rec. |
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| Is a | variable age at onset electroclinical syndrome | ||
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External Crossreferences & Linkouts
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GARD:7140 MESH:D020191 MIM:310370 MIM:PS254800 NCI:C7636 SNOMEDCT_US_2023_03_01:192844008 UMLS_CUI:C0751778 |
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