RS137852775 HADHA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Mitochondrial trifunctional protein deficiency
Inborn genetic diseases
Mitochondrial trifunctional protein deficiency 1
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Mitochondrial trifunctional protein deficiency
Inborn genetic diseases
Mitochondrial trifunctional protein deficiency 1
Other Variants in HADHA