3-methylcrotonyl-CoA carboxylase 1 deficiency (Q66299870)
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3-methylcrotonyl-CoA carboxylase deficiency that has material basis in homozygous or compound heterozygous mutation in the gene encoding the alpha subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 3q27
Language | Label | Description | Also known as |
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English | 3-methylcrotonyl-CoA carboxylase 1 deficiency |
3-methylcrotonyl-CoA carboxylase deficiency that has material basis in homozygous or compound heterozygous mutation in the gene encoding the alpha subunit of 3-methylcrotonyl-CoA carboxylase on chromosome 3q27 |
Statements
1 reference
Identifiers
1 reference
1 reference