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Sulfur metabolism disease

MONDO:0056803

A disease that has its basis in the disruption of sulfur compound metabolic process.

Also known as: disorder of sulfur compound metabolic process, disorder of sulfur metabolic process, disorder of sulfur metabolism, disorder of sulphur compound metabolic process, disorder of sulphur metabolic process, disorder of sulphur metabolism, sulfur compound metabolic process disease, sulphur compound metabolic process disease

22 clinical trials for this condition and its sub-types.

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Sub-types

Homocystinuria (5) Biotinidase deficiency (3) Hyperhomocysteinemia (3) Methylmalonic aciduria and homocystinuria type cblC (3) Classic homocystinuria (2) Methylcobalamin deficiency type cblE (2) Methylcobalamin deficiency type cblG (2) Methylmalonic aciduria and homocystinuria type cblD (2) Glutathione synthetase deficiency with 5-oxoprolinuria (1) Holocarboxylase synthetase deficiency (1) Homocystinuria due to methylene tetrahydrofolate reductase deficiency (1) Inherited glutathione synthetase deficiency (1) Methylmalonic acidemia with homocystinuria, type cblJ (1) Methylmalonic aciduria and homocystinuria (1) Methylmalonic aciduria and homocystinuria type cblF (1) Pyruvate dehydrogenase E3 deficiency (1) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (1) 5-oxoprolinase deficiency (0) Adenosine kinase deficiency (0) Autosomal recessive extra-oral halitosis (0)

Broader categories

Disease (618) Metabolic disease (215) Human disease (14) Mineral metabolism disease (1) Disease by developmental or physiological process (0)
Trials to join now! 13 Not yet recruiting 2 Not yet finished but already full! 3 Completed 4
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