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- Isobutyryl-coenzyme_A_dehydrogenase_deficiency abstract "Isobutyryl-coenzyme A dehydrogenase deficiency, commonly known as IBD 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 build up of valine in the urine, a symptom called valinuria.".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency diseasesdb "34225".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency omim "604773".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency thumbnail L-valine-skeletal.svg?width=300.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency wikiPageID "6040917".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency wikiPageRevisionID "544473314".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency caption Valine.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency diseasesdb "34225".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency hasPhotoCollection Isobutyryl-coenzyme_A_dehydrogenase_deficiency.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency name "Isobutyryl-coenzyme A dehydrogenase deficiency".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency omim "604773".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency wordnet_type synset-disease-noun-1.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency subject Category:Amino_acid_metabolism_disorders.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency subject Category:Autosomal_recessive_disorders.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type Abstraction100002137.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type AminoAcidMetabolismDisorders.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type Attribute100024264.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type AutosomalRecessiveDisorders.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type Condition113920835.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type Disorder114052403.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type PhysicalCondition114034177.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type State100024720.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type Disease.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type AilmentCondition.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency type Situation.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency comment "Isobutyryl-coenzyme A dehydrogenase deficiency, commonly known as IBD 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 build up of valine in the urine, a symptom called valinuria.".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency label "Isobutyryl-coenzyme A dehydrogenase deficiency".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency label "異丁酰輔酶A去氫酶缺乏症".
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency sameAs m.0fm09q.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency sameAs Q6085391.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency sameAs Q6085391.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency sameAs Isobutyryl-coenzyme_A_dehydrogenase_deficiency.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency wasDerivedFrom Isobutyryl-coenzyme_A_dehydrogenase_deficiency?oldid=544473314.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency depiction L-valine-skeletal.svg.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency isPrimaryTopicOf Isobutyryl-coenzyme_A_dehydrogenase_deficiency.
- Isobutyryl-coenzyme_A_dehydrogenase_deficiency name "Isobutyryl-coenzyme A dehydrogenase deficiency".