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Hypokalemic periodic paralysis
2 OMIM references -
3 associated genes
21 connected diseases
No signs/symptoms info
Disease Type of connection
Malignant hyperthermia
Acetazolamide-responsive myotonia
Brugada syndrome
Hyperkalemic periodic paralysis
Myotonia fluctuans
Myotonia permanens
Paramyotonia congenita of Von Eulenburg
Postsynaptic congenital myasthenic syndromes
Thyrotoxic periodic paralysis
Catecholaminergic polymorphic ventricular tachycardia
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant spastic paraplegia type 10
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
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
Romano-Ward syndrome
X-linked non-syndromic intellectual deficit
Synonym(s):
- Westphall disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: D020514
Gene symbol UniProt reference OMIM reference
CACNA1S Q13698114208
KCNE3 Q9Y6H6604433
SCN4A P35499603967
No signs/symptoms info available.