
Browsing Search Results
Search for 'compound_name:Sarcosine' in 'all pathways' in 'all' returned 66 results
SMP0125682 |
Metabolite
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
Homo sapiens
Disease
|
SMP0000570 |
Metabolite
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type
Homo sapiens
Disease
|
SMP0000340 |
Metabolite
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
Homo sapiens
Disease
|
SMP0120634 |
Metabolite
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type
Mus musculus
Disease
|
SMP0000341 |
Metabolite
Hypermethioninemia
Homo sapiens
Disease
|
SMP0120471 |
Metabolite
Cystathionine beta-Synthase Deficiency
Mus musculus
Disease
|
SMP0120487 |
Metabolite
Glycine N-Methyltransferase Deficiency
Mus musculus
Disease
|
SMP0125679 |
Metabolite
Hypermethioninemia
Homo sapiens
Disease
|
SMP0125684 |
Metabolite
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type
Homo sapiens
Disease
|
SMP0063637 |
Metabolite
Methionine Metabolism
Mus musculus
Metabolic
|