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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 diseasesdb "32207".
- 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 wikiPageRevisionID "575534547".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency caption Methylcrotonyl-CoA.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency diseasesdb "32207".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency hasPhotoCollection 3-Methylcrotonyl-CoA_carboxylase_deficiency.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency name "3".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency omim "210200".
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wordnet_type synset-disease-noun-1.
- 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 type Disease.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type AilmentCondition.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency type Situation.
- 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 m.0b6fq0.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency sameAs Q4634172.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency sameAs Q4634172.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency sameAs 5.
- 3-Methylcrotonyl-CoA_carboxylase_deficiency wasDerivedFrom 3-Methylcrotonyl-CoA_carboxylase_deficiency?oldid=575534547.
- 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".