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Hereditary Episodic Ataxia

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hereditary Episodic Ataxia is related to episodic ataxia and episodic ataxia, type 2, and has symptoms including ataxia, cerebellar ataxia and dysdiadochokinesis. An important gene associated with Hereditary Episodic Ataxia is SCN2A (Sodium Voltage-Gated Channel Alpha Subunit 2).
Related ID：
MALACARDS：HRD212
ICD11：423095680

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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2
17
2
HRD212

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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CAS Number
Status
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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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