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| Term | familial adult myoclonic epilepsy | ID (Ontology) | DOID:0111689 (Human Disease) | |||||
| Definition | An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities. | |||||||
| Also Known As | "BAFME" ; "benign adult familial myoclonic epilepsy" ; "benign adult familial myoclonus epilepsy" (for all, see Synonyms field below) | |||||||
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absence epilepsy |__adolescence-adult electroclinical syndrome |__familial adult myoclonic epilepsy 11 rec. |__familial adult myoclonic epilepsy 1 1 rec. |__familial adult myoclonic epilepsy 2 1 rec. |__familial adult myoclonic epilepsy 3 1 rec. |__familial adult myoclonic epilepsy 4 4 rec. |__familial adult myoclonic epilepsy 5 1 rec. |__familial adult myoclonic epilepsy 6 1 rec. |__familial adult myoclonic epilepsy 7 1 rec. |
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| Is a | adolescence-adult electroclinical syndrome | ||
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MIM:PS601068 ORDO:86814 SNOMEDCT_US_2023_03_01:717225001 UMLS_CUI:C4273988 |
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