Hyperkalemic periodic paralysis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
HYPERKALEMIC PERIODIC PARALYSIS
C0238357170500682MONDO:0008224
CLCN1 Causal
22649220 11840191 18337100
Disgenet
SCN4A Causal
1659948 1659668 15596759 17395131 20301669
Disgenet, GWAS catalog, HPO, Orphanet
All3 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Hyperkalemic periodic paralysis.
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Paramyotonia congenita 2 shared genesSCN4A, RANBP2 Related via 2 shared genes including SCN4A, RANBP2. Myotonia 1 shared geneSCN4A Related via 1 shared gene including SCN4A. Potassium-aggravated myotonia 1 shared geneSCN4A Related via 1 shared gene including SCN4A. SCN4A-related myopathy, autosomal recessive 1 shared geneSCN4A Related via 1 shared gene including SCN4A. familial acute necrotizing encephalopathy 1 shared geneRANBP2 Related via 1 shared gene including RANBP2.