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| Term | Unverricht-Lundborg syndrome | ID (Ontology) | DOID:3535 (Human Disease) |
| Definition | A progressive myoclonus epilepsy characterized by onset between 6 and 13 years of age of action- and stimulus-sensitive myoclonus, tonic-clonic seizures with ataxia, and a mild cognitive decline. | ||
| Also Known As | "Unverricht - Lundborg disease" ; "Unverricht's disease" ; "Unverricht-Lundborg disease" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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variable age at onset electroclinical syndrome |__progressive myoclonus epilepsy |__Unverricht-Lundborg syndrome 3 rec. |__progressive myoclonus epilepsy 1A |__progressive myoclonus epilepsy 1B 3 rec. |
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| Is a | progressive myoclonus epilepsy | ||
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External Crossreferences & Linkouts
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GARD:3876 MESH:D020194 NCI:C179710 SNOMEDCT_US_2023_03_01:192847001 UMLS_CUI:C0751785 |
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