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Longer titles found: Methylcrotonyl-CoA carboxylase (view), 3-Methylcrotonyl-CoA carboxylase deficiency (view)

searching for Methylcrotonyl-CoA 5 found (114 total)

List of diseases (0–9) (307 words) [view diff] case mismatch in snippet view article

deletion syndrome, rare (NIH) 3 alpha methylcrotonyl-Coa carboxylase 1 deficiency, rare (NIH) 3 alpha methylcrotonyl-coa carboxylase 2 deficiency, rare (NIH)

Biotin deficiency (2,733 words) [view diff] exact match in snippet view article find links to article

for five carboxylases in the human body (propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, pyruvate carboxylase, and 2 forms of acetyl-CoA carboxylase

Biotin—(methylcrotonoyl-CoA-carboxylase) ligase (177 words) [view diff] exact match in snippet view article

metabolism. Hopner T, Knappe J (1965). "[Synthesis of biotin in beta-methylcrotonyl-CoA-carboxylase by holocarboxylase synthetase]". Biochem. Z. 342 (2):

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

HIBCH 3-M syndrome; 273750; CUL7 3-Methylcrotonyl-CoA carboxylase 1 deficiency; 210200; MCCC1 3-Methylcrotonyl-CoA carboxylase 2 deficiency; 210210; MCCC2

B vitamins (2,802 words) [view diff] no match in snippet view article find links to article

acetate; pyruvate CoA carboxylase, involved in gluconeogenesis; β-methylcrotonyl CoA carboxylase, involved in the metabolism of leucine; and propionyl