Malonyl-CoA Decarboxylase Deficiency

About the Disease
Malonyl-Coa Decarboxylase Deficiency, also known as malonic aciduria, is related to atrial standstill 1 and inherited metabolic disorder, and has symptoms including abdominal pain, diarrhea and seizures. An important gene associated with Malonyl-Coa Decarboxylase Deficiency is MLYCD (Malonyl-CoA Decarboxylase). Affiliated tissues include heart, brain and liver, and related phenotypes are pachygyria and intellectual disability

Common Targets
MLYCD | BTD

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