Conditions / Genetic
molybdenum cofactor deficiency
info · Genetic · ICD-10: E72.1
A metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage.
Also known as: MOCOD; combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase