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 		0.010 GeneticVariation disease BEFREE Family with primary periodic paralysis and a mutation in MCM3AP, a gene implicated in mRNA transport. 31241196 2019