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Organic Acidemias

3-methylcrotonyl-CoA carboxylase (3MCC) deficiency
3-hydroxy-3-methylglutaryl (HMG)-CoA lyase deficiency
ß-ketothiolase deficiency
multiple carboxylase deficiency (MCD)
2-methyl-3-hydroxybutyric acidemia (2M3HBA)
3-methylglutaconic aciduria (3MGA)

If you have any questions please contact:

Integris Pediatric Specialty Clinic, Inborn Error of Metabolism (IEM) Clinic
Geneticist pager:  (405) 630-3794

OU Children’s Physicians – Genetics Clinic
Page Operator: (405) 271-3636

The Newborn Screening Program
Phone: (405) 271-6617 opt 2
Toll Free: (800) 766-2223 opt 2

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