Hypokalemic periodic paralysis Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14452)
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Genes

2 genes involed in the disease Hypokalemic periodic paralysis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
SCN4A sodium channel, voltage gated, type IV alpha subunit 5.0
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit 5.0