Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Primary episodic ataxias: diagnosis, pathogenesis and treatment. | 17575281 | 2007 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission. | 11723274 | 2001 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Identification of a novel nonsense mutation p.Tyr1957Ter of CACNA1A in a Chinese family with episodic ataxia 2. | 23441182 | 2013 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS. | 22249839 | 2012 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia. | 15710862 | 2005 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. | 9302278 | 1997 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | A pure cerebellar syndrome with corresponding ponto-cerebellar atrophy in acquired hepatocerebral degeneration. | 20233618 | 2010 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms. | 25735478 | 2015 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Clinical spectrum of episodic ataxia type 2. | 14718690 | 2004 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraine. | 23831250 | 2013 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia. | 9559993 | 1998 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies. | 27476654 | 2016 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. | 16325861 | 2006 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | The International Classification of Headache Disorders, 3rd edition (beta version). | 23771276 | 2013 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. | 8898206 | 1996 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2. | 11179022 | 2001 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Magnetic resonance imaging in familial paroxysmal ataxia. | 3358708 | 1988 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds. | 9436730 | 1998 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Migraine: gene mutations and functional consequences. | 17495624 | 2007 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Stepwise developmental regression associated with novel CACNA1A mutation. | 18940563 | 2008 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Sporadic hemiplegic migraine and delayed cerebral oedema after minor head trauma: a novel de novo CACNA1A gene mutation. | 19811514 | 2010 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood. | 18498393 | 2008 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | CaV2.1 channelopathies. | 20204399 | 2010 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. | 8988170 | 1997 | |||||
Muscle hypotonia
|
0.700 | CausalMutation | CLINVAR | Recurrent stroke due to a novel voltage sensor mutation in Cav2.1 responds to verapamil. | 21183743 | 2011 |