All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03601 CIAT cognitive impairment, ataxia, cerebellar (CIAT) 614306 AD 1 0 SCN8A - -
03678 DEE13 encephalopathy, developmental and epileptic, type 13 (DEE13) 614558 AD 2 2 SCN8A - -
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