All diseases

OMIM ID
231530
OMIM term:
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY
Alternative terms:
HADH DEFICIENCY
SCHAD DEFICIENCY, FORMERLY
(∗) Location:
4q25  
(†) Associated OMIM genes:
HADH  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/qt80zfe7