
Browsing Search Results
Search for 'compound_name:Sarcosine' in 'all pathways' in 'Homo sapiens' returned 29 results
SMP0125684 |
Disease
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type |
SMP0125681 |
Disease
Glycine N-Methyltransferase Deficiency |
SMP0000222 |
Disease
Glycine N-Methyltransferase Deficiency |
SMP0000177 |
Disease
Cystathionine beta-Synthase Deficiency |
SMP0000221 |
Disease
Methionine Adenosyltransferase Deficiency |
SMP0125678 |
Disease
Cystathionine beta-Synthase Deficiency |
SMP0125683 |
Disease
Methionine Adenosyltransferase Deficiency |
SMP0000004 |
Glycine and Serine Metabolism |
SMP0125580 |
Disease
Non-Ketotic Hyperglycinemia |
SMP0000242 |
Disease
Dimethylglycine Dehydrogenase Deficiency |