All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05802 DEE42;EIEE42 encephalopathy, developmental and epileptic, type 42 617106 AD 8 7 CACNA1A - -
01185 EA2 ataxia, episodic, type 2 108500 AD 9 4 CACNA1A - -
01362 FHM1 migraine, hemiplegic, familial, type 1 141500 AD 7 3 CACNA1A - -
01564 SCA6 ataxia, spinocerebellar, type 6 183086 AD 4 3 CACNA1A - -
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