3-methylcrotonyl-CoA Carboxylase Deficiency

About the Disease
3-Methylcrotonyl-Coa Carboxylase Deficiency, also known as 3-methylcrotonylglycinuria, is related to abdominal obesity-metabolic syndrome 1 and reye syndrome, and has symptoms including muscular hypotonia, muscular atrophy and feeding difficulties. An important gene associated with 3-Methylcrotonyl-Coa Carboxylase Deficiency is MCCC1 (Methylcrotonyl-CoA Carboxylase Subunit 1), and among its related pathways/superpathways are Disease and Metabolism. Affiliated tissues include cingulate cortex, kidney and lymph node, and related phenotypes are hypoglycemia and organic aciduria

Common Targets
MCCC2 | HGD | WDR72 | MCEE | MCCC1

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