| xanthinurie type II (aandoening) | | xanthinurie type II | | gecombineerde deficiëntie van xanthinedehydroxygenase en aldehydeoxidase
deficiëntie van molybdeencofactor
deficiëntie van cofactor molybdeen
molybdeencofactordeficiëntie
| | Combined molybdoflavoprotein enzyme deficiency | | Deficiency of molybdenum cofactor
Combined xanthine oxidase and aldehyde oxidase deficiency
Hereditary xanthinuria, type 2
Molybdenum cofactor deficiency
Combined xanthine oxidase and sulfite oxidase and aldehyde oxidase deficiency
Hereditary xanthinuria type 2
Xanthine oxidase-sulfite oxidase deficiency
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| | Id | 29692004 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | E79.8 | | Rule | TRUE | | Advice | ALWAYS E79.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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