Progressive Myoclonus Epilepsy 6
Disease ID: disease_node_16297
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| Dbxref | GARD:3872, MIM:614018, ORDO:280620 |
|---|---|
| Subclassof | DOID_891, DOID_0050737 |
| Data Source | DOID |
| Synonyms | EPM6, GOSR2-related progressive myoclonus ataxia, North Sea progressive myoclonus epilepsy, PME type 6, Progressive myoclonus epilepsy type 6 |
| Doid Label | progressive myoclonus epilepsy 6 |
| Doid Description | A progressive myoclonus epilepsy characterized by onset of ataxia in the first years of life, followed by action myoclonus and seizures later in childhood, and loss of independent ambulation in the second decade that has_material_basis_in homozygous or compound heterozygous mutation in the GOSR2 gene on chromosome 17q21.32. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16297 |
| Doid Id | DOID_0111449 |
| Label | Progressive Myoclonus Epilepsy 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)