Browsing Serum Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 369 - 372 of 479 in total
Combined oxidative phosphorylation deficiency 11 (614922 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 3200 uM | Abnormal | Newborn (0-30 days old) | Male | details |
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 |
Combined oxidative phosphorylation deficiency 14 (614946 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 4300 uM | Abnormal | Infant (0-1 year old) | Female | details |
Congenital cataracts, hearing loss, and neurodegeneration (614482 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Copper (HMDB0000657) | 4.878-11.645 uM | Abnormal | Infant (0-1 year old) | Male | details |