Sulfur metabolism disease
MONDO:0056803A 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
15 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Homocystinuria
(7)
Classic homocystinuria
(4)
Biotinidase deficiency
(3)
Hyperhomocysteinemia
(3)
Methylmalonic aciduria and homocystinuria type cblC
(3)
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)