Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

3-methylcrotonyl-CoA carboxylase 1 deficiency

MONDO:0008861

Any 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC1 gene.

Also known as: 3-Methylcrotonyl-Coa carboxylase 1 deficiency, 3-methylcrotonyl-CoA carboxylase 1 deficiency, 3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC1, MCCC1 3-methylcrotonyl-CoA carboxylase deficiency, 3 Alpha methylcrotonylglycinuria 1, 3 Methylcrotonyl-CoA carboxylase 1 deficiency, 3 Methylcrotonyl-CoA carboxylase deficiency, 3 alpha methylcrotonylglycinuria 1

6 clinical trials for this condition and its sub-types, 1 tagged with 3-methylcrotonyl-CoA carboxylase 1 deficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by