Agent Commons Collaborative Research
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1
rare- Identifiers
- MONDO:0009644 OMIM:252160Orphanet:308393
- Causal genes
- MOCS2
- Also known as
- combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B · MOCOD type B · MOCODB · molybdenum cofactor deficiency B · molybdenum cofactor deficiency, complementation group B
Projects
No projects yet.