FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term episodic ataxia type 1 ID (Ontology) DOID:0050989 (Human Disease)
Definition An episodic ataxia that is characterized by periodic ataxia and frequent myokymic discharges, and has_material_basis_in autosomal dominant inheritance of mutation in the potassium channel gene KCNA1.
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Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
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 Alleles Genes Human Disease Models
 episodic ataxia type 1       1      1      1
 for disease ribbon | episodic ataxia type 1       --       1       --
 model of | episodic ataxia type 1       1      1       --
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  hereditary ataxia
   |__episodic ataxia
       |__episodic ataxia type 1  3 rec.
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MIM:160120