All diseases

OMIM ID
250620
OMIM term:
BETA-HYDROXYISOBUTYRYL CoA DEACYLASE DEFICIENCY
Alternative terms:
3-@HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY
HIBCH DEFICIENCY
METHACRYLIC ACIDURIA
METHACRYLIC ACID TOXICITY
VALINE METABOLIC DEFECT
(∗) Location:
2q32.2  
(†) Associated OMIM genes:
HIBCH  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/j2zouyly