Episodic ataxia type 2
Also known as CACNA1A hereditary episodic ataxia, hereditary episodic ataxia caused by mutation in CACNA1A, APCA, Acetazolamide-responsive episodic ataxia syndrome+14 more
CACNA1A hereditary episodic ataxia, hereditary episodic ataxia caused by mutation in CACNA1A, APCA, Acetazolamide-responsive episodic ataxia syndrome, Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia, Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia, CAPA, Cerebellopathy, hereditary paroxysmal, EA2, Nystagmus-associated episodic ataxia, ataxia, episodic, with Nystagmus, ataxia, familial paroxysmal, ataxia, familial, paroxysmal, cerebellar ataxia, paroxysmal, Acetazolamide-responsive, episodic ataxia with nystagmus, episodic ataxia, Nystagmus-associated, episodic ataxia, type 2, familial paroxysmal ataxia.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Clinical trials
The current development programme across all trial phases.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
CACNA1A hereditary episodic ataxia, hereditary episodic ataxia caused by mutation in CACNA1A, APCA, Acetazolamide-responsive episodic ataxia syndrome, Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia, Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia, CAPA, Cerebellopathy, hereditary paroxysmal, EA2, Nystagmus-associated episodic ataxia, ataxia, episodic, with Nystagmus, ataxia, familial paroxysmal, ataxia, familial, paroxysmal, cerebellar ataxia, paroxysmal, Acetazolamide-responsive, episodic ataxia with nystagmus, episodic ataxia, Nystagmus-associated, episodic ataxia, type 2, familial paroxysmal ataxia
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Related entities are derived from literature co-mention (studied together) — associative, not causal.