Unverricht-Lundborg Syndrome
Disease ID: disease_node_10197
Connections displayed (default: 10).
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| Dbxref | GARD:3876, MESH:D020194, NCI:C179710, SNOMEDCT_US_2023_03_01:192847001, UMLS_CUI:C0751785 |
|---|---|
| Subclassof | DOID_891 |
| Data Source | DOID, MESH |
| Synonyms | Unverricht - Lundborg disease, Unverricht's disease, Unverricht-Lundborg disease |
| Mesh Id | D020194 |
| Mesh Label | Unverricht-Lundborg Syndrome |
| Mesh Subclassof | D020271, D020191 |
| Doid Label | Unverricht-Lundborg syndrome |
| Doid Description | 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. OMIM mapping confirmed by DO. [LS]. |
| Disease Node Id | disease_node_10197 |
| Doid Id | DOID_3535 |
| Label | Unverricht-Lundborg Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Progressive Myoclonus Epilepsy 1A(ID:disease_node_16293) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Progressive Myoclonus Epilepsy 1B(ID:disease_node_16294) (Disease)