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- Q4596905 subject Q6902466.
- Q4596905 subject Q7215445.
- Q4596905 subject Q8520454.
- Q4596905 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.".
- Q4596905 omim "610006".
- Q4596905 thumbnail 2-Methylbutanoyl-CoA.png?width=300.
- Q4596905 wikiPageWikiLink Q1707292.
- Q4596905 wikiPageWikiLink Q1758393.
- Q4596905 wikiPageWikiLink Q186380.
- Q4596905 wikiPageWikiLink Q219205.
- Q4596905 wikiPageWikiLink Q2305910.
- Q4596905 wikiPageWikiLink Q240642.
- Q4596905 wikiPageWikiLink Q243309.
- Q4596905 wikiPageWikiLink Q2725298.
- Q4596905 wikiPageWikiLink Q2813821.
- Q4596905 wikiPageWikiLink Q3278042.
- Q4596905 wikiPageWikiLink Q40924.
- Q4596905 wikiPageWikiLink Q41571.
- Q4596905 wikiPageWikiLink Q42918.
- Q4596905 wikiPageWikiLink Q4650492.
- Q4596905 wikiPageWikiLink Q484940.
- Q4596905 wikiPageWikiLink Q620730.
- Q4596905 wikiPageWikiLink Q6531938.
- Q4596905 wikiPageWikiLink Q6902466.
- Q4596905 wikiPageWikiLink Q7187.
- Q4596905 wikiPageWikiLink Q7215445.
- Q4596905 wikiPageWikiLink Q7574983.
- Q4596905 wikiPageWikiLink Q79749.
- Q4596905 wikiPageWikiLink Q8066.
- Q4596905 wikiPageWikiLink Q840737.
- Q4596905 wikiPageWikiLink Q8520454.
- Q4596905 name "2".
- Q4596905 omim "610006".
- Q4596905 type Disease.
- Q4596905 type Thing.
- Q4596905 type Q12136.
- Q4596905 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.".
- Q4596905 label "2-Methylbutyryl-CoA dehydrogenase deficiency".
- Q4596905 depiction 2-Methylbutanoyl-CoA.png.
- Q4596905 name "2-Methylbutyryl-CoA dehydrogenase deficiency".