Familial Hemiplegic Migraine 1
Disease ID: disease_node_20742
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| Dbxref | GARD:2638, MIM:141500 |
|---|---|
| Subclassof | DOID_0060178 |
| Data Source | DOID |
| Synonyms | FHM1, MHP1, familial hemiplegic migraine1 with progressive cerebellar ataxia |
| Doid Label | familial hemiplegic migraine 1 |
| Doid Description | A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13. |
| Disease Node Id | disease_node_20742 |
| Doid Id | DOID_0111181 |
| Label | Familial Hemiplegic Migraine 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Familial Hemiplegic Migraine(ID:disease_node_20739) (Disease)