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
03912 EEOC encephalopathy, epileptic, childhood-onset (EEOC) 615369 AD 11 7 CHD2 - -
06734 PARK22 Parkinson disease 22, autosomal dominant 616710 AD - - CHCHD2 - -
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