neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency (Q2823334)
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gene, encoding 3-hydroxyisobutyryl-CoA hydrolase; the mode of transmission has not yet been established.
- 3-Hydroxyisobutyryl-CoA Hydrolase Deficiency
- Methacrylic aciduria
- HIBCHD
- Valine Metabolic Defect
- HIBCH deficiency
- Beta-Hydroxyisobutyryl Coa Deacylase Deficiency
- Methacrylic Acid Toxicity
- 3-HYDROXYISOBUTYRYL-CoA HYDROLASE DEFICIENCY; HIBCHD
- 3-Hydroxyisobutyryl-CoA deacylase deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency |
gene, encoding 3-hydroxyisobutyryl-CoA hydrolase; the mode of transmission has not yet been established. |
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