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Thyrotoxic periodic paralysis
3 OMIM references -
3 associated genes
10 connected diseases
No signs/symptoms info
Disease Type of connection
Malignant hyperthermia
Hypokalemic periodic paralysis
Autosomal agammaglobulinemia
SHORT syndrome
Autosomal dominant centronuclear myopathy
Benign Samaritan congenital myopathy
Central core disease
Congenital multicore myopathy with external ophthalmoplegia
King-Denborough syndrome
Moderate multiminicore disease with hand involvement
Synonym(s):
- Thyrotoxic hypokalemic periodic paralysis
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: sporadic
External references:
3 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
CACNA1S Q13698114208
GABRA3 P34903305660
KCNJ18 B7U540613236
No signs/symptoms info available.