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
05519 AOA ataxia-oculomotor apraxia (AOA) - - 15 14 APTX, PIK3R5, PNKP, SETX - -
00853 AOA3 ataxia-oculomotor apraxia, type 3 (AOA-3) 615217 AR 1 1 PIK3R5 - -
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