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, 0 tagged with Sulfur metabolism disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Sulfur metabolism disease
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Inborn disorder of methionine cycle and sulfur amino acid metabolism 0 trials · 11 incl. sub-types
6 sub-types
- Homocystinuria 7 trials · 11 incl. sub-types Sub-types →
- Encephalopathy due to sulfite oxidase deficiency 0 trials · 1 incl. sub-types Sub-types →
- Autosomal recessive extra-oral halitosis 0 trials
- Cystathioninuria 0 trials
- Disorder of methionine catabolism 0 trials Sub-types →
- Methionine adenosyltransferase deficiency 0 trials
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Biotin metabolic disease 0 trials · 3 incl. sub-types
2 sub-types
- Inborn error of biotin metabolism 0 trials · 3 incl. sub-types Sub-types →
- Nutritional biotin deficiency 0 trials
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Inherited glutathione metabolism disease 0 trials · 1 incl. sub-types
6 sub-types
- Inherited glutathione synthetase deficiency 1 trial Sub-types →
- 5-oxoprolinase deficiency 0 trials
- Gamma-glutamyl transpeptidase deficiency 0 trials
- Gamma-glutamylcysteine synthetase deficiency 0 trials
- Hemolytic anemia due to glutathione reductase deficiency 0 trials
- Spondylometaphyseal dysplasia, Sedaghatian type 0 trials
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Inherited lipoic acid biosynthesis defect 0 trials · 1 incl. sub-types
6 sub-types
- Pyruvate dehydrogenase E3 deficiency 1 trial
- Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities 0 trials
- Fatal multiple mitochondrial dysfunctions syndrome 0 trials Sub-types →
- Lipoic acid synthetase deficiency 0 trials
- Lipoyl transferase 1 deficiency 0 trials
- Spasticity-ataxia-gait anomalies syndrome 0 trials
Most studied deeper sub-types
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)
Methylmalonic acidemia with homocystinuria, type cblJ
(1)
Methylmalonic aciduria and homocystinuria
(1)
Methylmalonic aciduria and homocystinuria type cblF
(1)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A
(1)
Adenosine kinase deficiency
(0)
Glutathione synthetase deficiency without 5-oxoprolinuria
(0)
Glycine N-methyltransferase deficiency
(0)
Homocystinuria-megaloblastic anemia cblD type
(0)
Homocystinuria without methylmalonic aciduria
(0)
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase
(0)