All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04630 BFIS2 Seizures, benign familial infantile, type 2 (BFIS-2) 605751 AD 7 6 PRRT2 - -
01295 DYT10 dystonia, type 10 (DYT-10) 128200 AD 6 6 PRRT2 - -
04629 ICCA convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA) 602066 AD 7 6 PRRT2 - -
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