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Up to: Mineral metabolism disease
Sulfur metabolism disease
A disease that has its basis in the disruption of sulfur compound metabolic process.
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Inborn disorder of methionine cycle and sulfur amino acid metabolism 0 trials · 11 incl. sub-types Sub-types →
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Biotin metabolic disease 0 trials · 3 incl. sub-types Sub-types →
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Inherited glutathione metabolism disease 0 trials · 1 incl. sub-types Sub-types →
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Inherited lipoic acid biosynthesis defect 0 trials · 1 incl. sub-types Sub-types →