Inborn disorder of methionine cycle and sulfur amino acid metabolism

MONDO:0019222

An inherited metabolic disease that is has its basis in the disruption of sulfur amino acid metabolic process.

Also known as: cytosolic methyl group transfer or sulfur amino acid metabolism disorder, cytosolic methyl group transfer or sulphur amino acid metabolism disorder, inborn error of sulfur amino acid metabolic process, inborn error of sulphur amino acid metabolic process, inborn sulfur amino acid metabolic process disorder, inborn sulphur amino acid metabolic process disorder, rare inborn error of sulfur amino acid metabolic process, rare inborn error of sulphur amino acid metabolic process

12 clinical trials for this condition and its sub-types, 0 tagged with Inborn disorder of methionine cycle and sulfur amino acid metabolism itself.

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Where it sits in the disease tree

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Part of

↑ Inborn disorder of amino acid and other organic acid metabolism (225) ↑ Disorder of organic acid metabolism (154) ↑ Sulfur metabolism disease (14)

Sub-types of Inborn disorder of methionine cycle and sulfur amino acid metabolism

Homocystinuria 7 trials · 11 incl. sub-types
5 sub-types
- Classic homocystinuria 4 trials
- Hyperhomocysteinemia 3 trials
- Methylmalonic aciduria and homocystinuria 1 trial · 3 incl. sub-types Sub-types →
- Homocystinuria without methylmalonic aciduria 0 trials · 2 incl. sub-types Sub-types →
- Homocystinuria due to methylene tetrahydrofolate reductase deficiency 1 trial
Encephalopathy due to sulfite oxidase deficiency 0 trials · 1 incl. sub-types
2 sub-types
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency 0 trials · 1 incl. sub-types Sub-types →
- Isolated sulfite oxidase deficiency 0 trials
Autosomal recessive extra-oral halitosis 0 trials
Cystathioninuria 0 trials
Disorder of methionine catabolism 0 trials
3 sub-types
- Adenosine kinase deficiency 0 trials
- Glycine N-methyltransferase deficiency 0 trials
- Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase 0 trials
Methionine adenosyltransferase deficiency 0 trials

Most studied deeper sub-types

Methylmalonic aciduria and homocystinuria type cblC (3) Methylcobalamin deficiency type cblE (2) Methylcobalamin deficiency type cblG (2) Methylmalonic aciduria and homocystinuria type cblD (2) Methylmalonic acidemia with homocystinuria, type cblJ (1) Methylmalonic aciduria and homocystinuria type cblF (1) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (1) Homocystinuria-megaloblastic anemia cblD type (0) Methylcobalamin deficiency type cblDv1 (0) Methylmalonic acidemia with homocystinuria, type cblX (0) Methylmalonic aciduria and homocystinuria, cb1L type (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1 (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2 (0) Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C (0)

Including sub-types (12) Tagged with Inborn disorder of methionine cycle and sulfur amino acid metabolism (0)

Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 3 Completed 3

Inborn disorder of methionine cycle and sulfur amino acid metabolism

Where it sits in the disease tree

Most studied deeper sub-types

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Mapping homocystinuria: how does this rare metabolic disorder unfold over a lifetime?

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