Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/3-Methylcrotonyl-CoA_carboxylase_deficiency> ?p ?o }
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- 3-Methylcrotonyl-CoA_carboxylase_deficiency abstract "3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency), also known as 3-Methylcrotonylglycinuria or BMCC deficiency is an inherited disorder in which the body is unable to process certain proteins properly. People with this disorder have inadequate levels of an enzyme that helps break down proteins containing the amino acid leucine. This condition affects an estimated 1 in 50,000 individuals worldwide.".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency omim "210200".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency thumbnail Methylcrotonyl_coenzyme_A.svg?width=300.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageExternalLink ghr.nlm.nih.gov.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageID "3911266".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageLength "4548".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageOutDegree "22".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageRevisionID "664763434".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Amino_acid.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Biotin.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Biotinidase_deficiency.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Brain.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Category:Autosomal_recessive_disorders.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Diarrhea.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Gene.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Genetic_disorder.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Holocarboxylase_synthetase_deficiency.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Hypotonia.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Lethargy.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Leucine.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Methylcrotonyl-CoA.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Methylcrotonyl-CoA_carboxylase.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Multiple_carboxylase_deficiency.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Nervous_system.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Newborn_screening.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLink Reye_syndrome.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLinkText "3-Methylcrotonyl-CoA carboxylase deficiency".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageWikiLinkText "MCC-deficient syndrome".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency caption Methylcrotonyl-CoA.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency diseasesdb "32207".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency name "3".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency omim "210200".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageUsesTemplate Template:Amino_acid_metabolic_pathology.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageUsesTemplate Template:Morefootnotes.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageUsesTemplate Template:NLM.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageUsesTemplate Template:OMIM2.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wikiPageUsesTemplate Template:Reflist.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency subject Category:Amino_acid_metabolism_disorders.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency subject Category:Autosomal_recessive_disorders.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency hypernym Disorder.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Disease.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Defect.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Disorder.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Error.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Pediatric.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Redirect.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Thing.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Q12136.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency comment "3-Methylcrotonyl-CoA carboxylase deficiency (3MCC deficiency), also known as 3-Methylcrotonylglycinuria or BMCC deficiency is an inherited disorder in which the body is unable to process certain proteins properly. People with this disorder have inadequate levels of an enzyme that helps break down proteins containing the amino acid leucine. This condition affects an estimated 1 in 50,000 individuals worldwide.".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency label "3-Methylcrotonyl-CoA carboxylase deficiency".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency sameAs Q4634172.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency sameAs m.0b6fq0.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency sameAs Q4634172.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wasDerivedFrom 3-Methylcrotonyl-CoA_carboxylase_deficiency?oldid=664763434.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency depiction Methylcrotonyl_coenzyme_A.svg.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency isPrimaryTopicOf 3-Methylcrotonyl-CoA_carboxylase_deficiency.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency name "3-Methylcrotonyl-CoA carboxylase deficiency".