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- 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 diseasesdb "34413".
- 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 wikiPageRevisionID "604790867".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency caption "2".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency diseasesdb "34413".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency hasPhotoCollection 2-Methylbutyryl-CoA_dehydrogenase_deficiency.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency name "2".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency omim "610006".
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wordnet_type synset-disease-noun-1.
- 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 type Disease.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type AilmentCondition.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency type Situation.
- 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 m.0dd3gm.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency sameAs Q4596905.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency sameAs Q4596905.
- 2-Methylbutyryl-CoA_dehydrogenase_deficiency wasDerivedFrom 2-Methylbutyryl-CoA_dehydrogenase_deficiency?oldid=604790867.
- 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".