Thyrotoxic periodic paralysis Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations 2025
Category disease or phenotype associations
Type phenotype
Description Thyrotoxic periodic paralysis (TPP) is a rare neurological disease characterized by recurrent episodes of paralysis and hypokalemia during a thyrotoxic state. (Orphanet Rare Disease Ontology, Orphanet_79102)
External Link http://purl.obolibrary.org/obo/MONDO_0019201
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Genes

2 genes associated with the Thyrotoxic periodic paralysis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Symbol Name Standardized Value
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2 2.1
TRIM2 tripartite motif containing 2 0.852288