G2Cdb::Human Disease report
- Disease id
- D00000210
- Name
- Thyrotoxic periodic paralysis
- Nervous system disease
- no
Genes (1)
| Gene | Name/Description | Mutations Found | Literature | Mutations Type | Genetic association? |
|---|---|---|---|---|---|
| G00001324 | ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide |
Y | (15001631) | Single nucleotide polymorphism (SNP) | N |