myICD10.com Logo
multiple acyl-coa dehydrogenase deficiency

Medical Definition

An autosomal recessive disorder of fatty acid oxidation, and branched chain amino acids (amino acids, branched-chain); lysine; and choline catabolism, that is due to defects in either subunit of electron transfer flavoprotein or its dehydrogenase, electron transfer flavoprotein-ubiquinone oxidoreductase (ec 1.5.5.1).
Related Codes (1)
Code
Description
Billable
Details
E71.313Glutaric aciduria type II
Type 1 Excludes (1)

Rows per page

Page 1 of 1