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
06770 EIEE76 Epileptic encephalopathy, early infantile, 76 618468 AR - - ACTL6B - -
05944 IDDSSAD intellectual developmental disorder with severe speech and ambulation defects (IDDSSAD) 618470 AD - - ACTL6B - -
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