molybdenum cofactor deficiency type B (Q50349829)
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molybdenum cofactor deficiency that has material basis in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11
- combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B
- MOCOD type B
- molybdenum cofactor deficiency complementation group B
- MOCODB
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | molybdenum cofactor deficiency type B |
molybdenum cofactor deficiency that has material basis in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11 |
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