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
02422 ALS4 sclerosis, lateral, amyotrophic, type type 4 (ALS4) 602433 AD 3 3 SETX - -
05519 AOA ataxia-oculomotor apraxia (AOA) - - 15 14 APTX, PIK3R5, PNKP, SETX - -
02569 SCAN2;SCAR1;AOA2 ataxia, spinocerebellar, autosomal recrecessive, with axonal neuropathy, type 2 (SCAR1, AOA2) 606002 AR 74 74 SETX - autosomal recessive
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