(Q50349834)
English
molybdenum cofactor deficiency type C
molybdenum cofactor deficiency that has material basis in homozygous mutation in the GPHN gene on chromosome 14q23
- molybdenum cofactor deficiency complementation group C
- MOCODC
- combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C
- MOCOD type C
Statements
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Identifiers
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