2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency or MBHD, is an inherited disorder in which the body is unable to process the amino acid isoleucine properly.

PropertyValue
dbpedia-owl:Disease/diseasesdb
  • 34413
dbpedia-owl:Disease/omim
  • 610006
dbpedia-owl:diseasesdb
  • 34413
dbpedia-owl:omim
  • 610006
dbpedia-owl:thumbnail
dbpprop:abstract
  • 2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency or MBHD, is an inherited disorder in which the body is unable to process the amino acid isoleucine properly.
dbpprop:caption
dbpprop:diseasesdb
  • 34413 (xsd:integer)
dbpprop:hasPhotoCollection
dbpprop:image
  • 2-Methylbutanoyl-CoA.png
dbpprop:name
  • 2-Methylbutyryl-CoA dehydrogenase deficiency
dbpprop:omim
  • 610006 (xsd:integer)
dbpprop:reference
dbpprop:wikiPageUsesTemplate
dbpprop:wordnet_type
rdf:type
rdfs:comment
  • 2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency or MBHD, is an inherited disorder in which the body is unable to process the amino acid isoleucine properly.
rdfs:label
  • 2-Methylbutyryl-CoA dehydrogenase deficiency
owl:sameAs
skos:subject
foaf:depiction
foaf:name
  • 2-Methylbutyryl-CoA dehydrogenase deficiency
foaf:page
is dbpprop:redirect of
is owl:sameAs of