Additional Disease Briefs

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* = NORD Rare Disease Report

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Rare Disease Database Reports Additional Rare Disease Briefs
episodic ataxia type 3

Also known as: EA3, ataxia, episodic, with vertigo and tinnitus, episodic ataxia, type 3, episodic ataxia-vertigo-tinnitus-myokymia syndrome

episodic ataxia type 4

Also known as: EA4, PATX, ataxia, periodic vestibulocerebellar, episodic ataxia, type 4, periodic vestibulocerebellar ataxia

episodic ataxia type 5

Also known as: CACNB4 hereditary episodic ataxia, EA5, episodic ataxia, type 5, hereditary episodic ataxia caused by mutation in CACNB4

episodic ataxia type 6

Also known as: EA6, SLC1A3 hereditary episodic ataxia, episodic ataxia type 6, episodic ataxia, type 6, hereditary episodic ataxia caused by mutation in SLC1A3

episodic ataxia type 8

Also known as: EA8, episodic ataxia type 8, episodic ataxia with slurred speech, episodic ataxia, type 8

episodic kinesigenic dyskinesia 1

Also known as: DYT-PRRT2, EKD1, PRRT2 episodic kinesigenic dyskinesia, PxMD-PRRT2, dystonia 10, dystonia, familial paroxysmal, episodic kinesigenic dyskinesia 1, episodic kinesigenic dyskinesia caused by mutation in PRRT2, episodic kinesigenic dyskinesia type 1, paroxysmal kinesigenic choreoathetosis, paroxysmal kinesigenic dyskinesia

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