| Symbol
| MHP2
|
| Location
| 1q23.2
|
| Name
|
migraine familial hemiplegic, 2 |
| Other name(s)
|
migraine familial basilar |
| Corresponding gene
|
ATP1A2
|
| Other symbol(s)
| FHM2, AHC
|
| Main clinical features
|
migraine with aura, associated with hemiparesis during the aura, with epileptic seizures during severe migraine attacks in some patients |
| Genetic determination
| autosomal dominant |
| Related entries
| including forms with episodes of both very severe and transient neurological symptoms that were triggered by mild head trauma as well as permanent mental retardation
|
| Function/system disorder
| neurology |
| Type
| disease
|