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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Developmental anomaly of metabolic origin
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Encephalopathy due to sulfite oxidase deficiency
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Sulfite oxidase deficiency due to molybdenum cofactor deficiency
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2
rare
Identifiers
MONDO:0980701
OMIM:621373
Causal genes
MOCS3
Part of
Sulfite oxidase deficiency due to molybdenum cofactor deficiency
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