Chapter 3 - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)»Certain disorders involving the immune mechanism (D80-D89)»Other biotin-dependent carboxylase deficiency (D81.818)
D81.818
Other biotin-dependent carboxylase deficiency
Related indications (MeSH) (1)
The neonatal form of MULTIPLE CARBOXYLASE DEFICIENCY that is caused by a defect or deficiency in holocarboxylase synthetase. HLCS is the enzyme that covalently links biotin to the biotin dependent carboxylases (propionyl-CoA-carboxylase, pyruvate carboxylase, and beta-methylcrotonyl-CoA carboxylase).