All diseases

7 entries on 1 page. Showing entries 1 - 7.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01815 - 3-hydroxyacyl-CoA dehydrogenase deficiency 231530 AR - - HADH - -
04028 FRTS3 Fanconi renotubular syndrome, type 3 (FRTS-3) 615605 AD - - EHHADH - -
02889 HHF4 Hyperinsulinemic hypoglycemia, familial, 4 609975 AR - - HADH - -
02812 LCHADD LCHAD deficiency 609016 AR 29 29 HADHA - -
02811 MTPD mitochondrial trifunctional protein deficiency - - 160 155 HADHA, HADHB - -
07124 MTPD1 mitochondrial trifunctional protein deficiency, type 1 609015 AR - - HADHA - -
07123 MTPD2 mitochondrial trifunctional protein deficiency, type 2 620300 AR - - HADHB - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.