Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/2-Methylbutyryl-CoA_dehydrogenase_deficiency> ?p ?o }
Showing triples 1 to 60 of
60
with 100 triples per page.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency abstract "2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methylbutyryl glycinuria or short/branched-chain acyl-CoA dehydrogenase deficiency (SBCADD), is an autosomal recessive metabolic disorder. It causes the body to be unable to process the amino acid isoleucine properly. Initial case reports identified individuals with developmental delay and epilepsy, however most cases identified through newborn screening have been asymptomatic.".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency omim "610006".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency thumbnail 2-Methylbutanoyl-CoA.png?width=300.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageID "5295660".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageLength "5560".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageOutDegree "31".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageRevisionID "695598713".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink 2-Methylbutyryl-CoA.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink ACADSB.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Amino_acid.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Asymptomatic.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Autosome.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Blood_plasma.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Carnitine.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Category:Autosomal_recessive_disorders.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Category:Hmong.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Chromosome_10_(human).
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Dominance_(genetics).
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Epilepsy.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Gene.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Glycine.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Hmong_people.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Inborn_error_of_metabolism.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Isoleucine.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Isovaleric_acidemia.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Mutation.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Newborn_screening.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Sampling_bias.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Specific_developmental_disorder.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Urine.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink Valproate.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLink File:Autosomal_recessive_-_en.svg.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageWikiLinkText "2-Methylbutyryl-CoA dehydrogenase deficiency".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency caption "2".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency diseasesdb "34413".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency name "2".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency omim "610006".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageUsesTemplate Template:Amino_acid_metabolic_pathology.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageUsesTemplate Template:Reflist.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wikiPageUsesTemplate Template:Research_help.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency subject Category:Amino_acid_metabolism_disorders.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency subject Category:Autosomal_recessive_disorders.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency subject Category:Hmong.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency hypernym Disorder.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type Disease.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type Disorder.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type Error.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type Thing.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type Q12136.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency comment "2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methylbutyryl glycinuria or short/branched-chain acyl-CoA dehydrogenase deficiency (SBCADD), is an autosomal recessive metabolic disorder. It causes the body to be unable to process the amino acid isoleucine properly. Initial case reports identified individuals with developmental delay and epilepsy, however most cases identified through newborn screening have been asymptomatic.".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency label "2-Methylbutyryl-CoA dehydrogenase deficiency".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency sameAs Q4596905.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency sameAs m.0dd3gm.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency sameAs Q4596905.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wasDerivedFrom 2-Methylbutyryl-CoA_dehydrogenase_deficiency?oldid=695598713.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency depiction 2-Methylbutanoyl-CoA.png.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency isPrimaryTopicOf 2-Methylbutyryl-CoA_dehydrogenase_deficiency.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency name "2-Methylbutyryl-CoA dehydrogenase deficiency".