RS121918243 MMACHC
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What This Variant Does
"[OMIM:?]
Associated Conditions
Cobalamin C disease
Inborn genetic diseases
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Disorders of Intracellular Cobalamin Metabolism
MMACHC-related disorder
Cobalamin C disease
Cobalamin C disease
Inborn genetic diseases
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Disorders of Intracellular Cobalamin Metabolism
MMACHC-related disorder
Cobalamin C disease
Other Variants in MMACHC