Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 555941 | cacna1ba | calcium channel, voltage-dependent, N type, alpha 1B subunit, a | |
| 562059 | cacna1aa | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, a | |
| 569528 | cacna1ab | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b |
