RS387906297 ACADM
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What This Variant Does
"CLNSIG=5
Associated Conditions
Medium-chain acyl-coenzyme A dehydrogenase deficiency
ACADM-related disorder
Inborn genetic diseases
MCADD - Medium-chain acyl-CoA dehydrogenase deficiency – full ACADM sequencing newborn screening follow up
Medium-chain acyl-coenzyme A dehydrogenase deficiency
ACADM-related disorder
Inborn genetic diseases
MCADD - Medium-chain acyl-CoA dehydrogenase deficiency – full ACADM sequencing newborn screening follow up
Other Variants in ACADM