Disease #03175 (EA6 (ataxia, episodic, type 6 (EA-6)), OMIM:612656)

Official abbreviation EA6
Name ataxia, episodic, type 6 (EA-6)
OMIM ID 612656
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SLC1A3
Associated tissues -
Disease features -
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Individuals

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00385118 184722 - - F no Germany - - - - - EA6 Vestibular dysfunction, Vestibular hypofunction, Episodic ataxia, Headache, Vertigo SLC1A3 SLC1A3 1 1 Andreas Laner
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