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- Isobutyryl-coenzyme A dehydrogenase deficiency is a rare metabolic disorder in which the body is unable to process certain amino acids properly. People with this disorder have inadequate levels of an enzyme that helps break down the amino acid valine, resulting in a buildup of valine in the urine, a symptom called . (en)
- 異丁酰輔酶A去氫酵素缺乏症（英語：Isobutyryl-coenzyme A dehydrogenase deficiency）是一種遺傳病，其會導致患者無法製造出正確的蛋白質，使不能充分分解纈氨酸。 此遺傳病報告過的個案少於5宗，極罕見。 遺傳方面，其遺傳方式為自體隱性遺傳疾病，造成變異。 (zh)
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- 3656 (xsd:nonNegativeInteger)
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- Isobutyryl-coenzyme A dehydrogenase deficiency (en)
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- Isobutyryl-coenzyme A dehydrogenase deficiency is a rare metabolic disorder in which the body is unable to process certain amino acids properly. People with this disorder have inadequate levels of an enzyme that helps break down the amino acid valine, resulting in a buildup of valine in the urine, a symptom called . (en)
- 異丁酰輔酶A去氫酵素缺乏症（英語：Isobutyryl-coenzyme A dehydrogenase deficiency）是一種遺傳病，其會導致患者無法製造出正確的蛋白質，使不能充分分解纈氨酸。 此遺傳病報告過的個案少於5宗，極罕見。 遺傳方面，其遺傳方式為自體隱性遺傳疾病，造成變異。 (zh)
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- Isobutyryl-coenzyme A dehydrogenase deficiency (en)
- 異丁酰輔酶A去氫酶缺乏症 (zh)
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- Isobutyryl-coenzyme A dehydrogenase deficiency (en)
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