Disease: Episodic Ataxia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		0.010 GeneticVariation disease BEFREE Two PRRT2 mutations were in familial hemiplegic migraine or episodic ataxia, one SLC2A1 family had episodic ataxia and one PNKD family had familial hemiplegic migraine alone. 26598494 2015