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bn:01316910n
Noun Concept
Categories: Vitamin, coenzyme, and cofactor metabolism disorders
EN
molybdenum cofactor deficiency  combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase  MOCOD
EN
Molybdenum cofactor deficiency is a rare human disease in which the absence of molybdopterin – and consequently its molybdenum complex, commonly called molybdenum cofactor – leads to accumulation of toxic levels of sulphite and neurological damage. Wikipedia
Definitions
Relations
Sources
EN
Molybdenum cofactor deficiency is a rare human disease in which the absence of molybdopterin – and consequently its molybdenum complex, commonly called molybdenum cofactor – leads to accumulation of toxic levels of sulphite and neurological damage. Wikipedia
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 Wikidata
IS A
rare disease
metal metabolism disorder
GENETIC ASSOCIATION
MOCS1
Wikipedia
EN
molybdenum cofactor deficiency
Wikidata
EN
Molybdenum cofactor deficiency
Wikidata Alias
EN
combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase, MOCOD, molybdenum cofactor deficiency

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