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
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 - -
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