molybdenum cofactor deficiency type B
Disease
molybdenum cofactor deficiency type B
- Definition
A molybdenum cofactor deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the MOCS2 gene on chromosome 5q11.
- Synonyms
- combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B
- MOCOD type B
- Cross References
- Parent Terms
- Child Terms
- None
- Sources of Associations
Associated Genes
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