Disease: Familial Periodic Paralysis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		0.110 GeneticVariation disease BEFREE Sporadic periodic paralysis (SPP), the second leading cause of hypokalemic periodic paralysis (HPP) in Asia, has a presentation similar to that of familial periodic paralysis (FPP) and is caused by gene mutations in the calcium (Ca(2+)) (CACNA1S) and sodium (Na(+)) (SCN4A) channels of skeletal muscle. 21841462 2012
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		0.110 Biomarker disease HPO