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
01625 ACADSD Acyl-CoA dehydrogenase, short-chain, deficiency of 201470 AR 3 3 ACADS - -
00172 SBCADD 2-methylbutyryl-CoA dehydrogenase deficiency (SBCADD) 610006 AR 24 24 ACADSB - -
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