All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01815 - 3-hydroxyacyl-CoA dehydrogenase deficiency 231530 - 0 0 HADH - -
02811 - mitochondrial trifunctional protein deficiency (MTPD) 609015 - 3 3 HADHA, HADHB - -
02812 - long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 609016 - 1 1 HADHA - -
02889 - Hyperinsulinemic hypoglycemia, familial, 4 609975 - 0 0 HADH - -
04028 FRTS-3 Fanconi renotubular syndrome, type 3 (FRTS-3) 615605 - 0 0 EHHADH - -
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