Orphanet: Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

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Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

ORPHA:308400

Classification level: Subtype of disorder

Synonym(s):
- Combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C
- MOCOD type C
Prevalence: -
Inheritance: -
Age of onset: -
ICD-10: E72.1
OMIM: 615501
UMLS: C1854990
MeSH: -
GARD: -
MedDRA: -

Summary

This disease is described under Encephalopathy due to sulfite oxidase deficiency

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