Episodic ataxia type 3

Episodic ataxia type 3 (EA3) is a very rare form of Hereditary episodic ataxia (see this term) characterized by vestibular ataxia, vertigo, tinnitus, and interictal myokymia.



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Total: 0 (papers)
  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
        

Phenotype(s) retrieved from Orphanet

    Total: 9

HPO ID Term Frequency
HP:0002131 Episodic ataxia Obligate (100%)
HP:0002321 Vertigo Obligate (100%)
HP:0000360 Tinnitus Frequent (79-30%)
HP:0002411 Myokymia Frequent (79-30%)
HP:0000639 Nystagmus Occasional (29-5%)
HP:0001250 Seizures Occasional (29-5%)
HP:0002301 Hemiplegia Occasional (29-5%)
HP:0002076 Migraine Excluded (0%)
HP:0002315 Headache Excluded (0%)


Phenotype(s) retrieved from case reports

    Total: 0

HPO ID Term # of case reports


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID