Browsing Serum Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 377 - 380 of 479 in total
Combined oxidative phosphorylation deficiency 12 (614924 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 6500 uM | Abnormal | Infant (0-1 year old) | Male | details |
Epileptic encephalopathy, early infantile, 39 (612949 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 6000 uM | Abnormal | Children (1-13 years old) | Female | details |
Fructose intolerance, hereditary (229600 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 5200 uM | Abnormal | Children (1-13 years old) | Male | details |
Hyperglycinemia, lactic acidosis, and seizures (614462 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 4600-57700 uM | Abnormal | Newborn (0-30 days old) | Male | details | |
| Glycine (HMDB0000123) | 906 uM | Abnormal | Newborn (0-30 days old) | Male | details |