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MIRAGE
familial hemiplegic migraine 1
Summary
- Synonym
-
- FHM1
- MHP1
- familial hemiplegic migraine1 with progressive cerebellar ataxia
- Definition
- A familial hemiplegic migraine that is commonly associated with cerebellar degeneration and has_material_basis_in heterozygous mutation in CACNA1A on 19p13.
- Super Class
- familial hemiplegic migraine
External Links
- Disease Ontology
- DOID:0111181
- Mondo Disease Ontology
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O00555 | Voltage-dependent P/Q-type calcium channel subunit alpha-1A |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q59E53 | Cacophony, isoform H |
