Hyperkalemic periodic paralysis

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FAMILIAL HYPERKALEMIC PERIODIC PARALYSIS
NBK1496
SCN4A Unknown — ClinVar
HYPERKALEMIC PERIODIC PARALYSIS
C0238357170500682MONDO:0008224
CLCN1 Causal
22649220 11840191 18337100
Disgenet
SCN4A Causal
1659948 1659668 15596759 17395131 20301669
Disgenet, GWAS catalog, HPO, Orphanet
RANBP2 Unknown — Disgenet
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.