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
06085 CADEDS Cerebellar atrophy, developmental delay, and seizures 617643 AR - - KCNMA1 - -
06095 EIG16 {Epilepsy, idiopathic generalized, susceptibility to, 16} 618596 AD - - KCNMA1 - -
06100 LIWAS Liang-Wang syndrome 618729 AD 2 1 KCNMA1 - -
02852 PNKD3;GEPD dyskinesia, nonkinesigenic, paroxysmal, type 3, with/without generalized epilepsy (PNKD-3, generalized epilepsy and paroxysmal dyskinesia(GEPD)) 609446 AD - - KCNMA1 - -
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