Browsing Serum Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 473 - 476 of 479 in total
Phosphoserine Aminotransferase Deficiency (610992 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Glycine (HMDB0000123) | 121 uM | Abnormal | Infant (0-1 year old) | Male | details | |
| Glycine (HMDB0000123) | 110 uM | Abnormal | Newborn (0-30 days old) | Female | details | |
| Serine (HMDB0000187) | 51 uM | Abnormal | Infant (0-1 year old) | Male | details | |
| Serine (HMDB0000187) | 30 uM | Abnormal | Newborn (0-30 days old) | Female | details |
Phosphoserine Phosphatase Deficiency (614023 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Glycine (HMDB0000123) | 77-97 uM | Abnormal | Infant (0-1 year old) | Male | details | |
| Serine (HMDB0000187) | 29-55 uM | Abnormal | Infant (0-1 year old) | Male | details | |
| Serine (HMDB0000187) | 53-80 uM | Abnormal | Children (1-13 years old) | Male | details | |
| Serine (HMDB0000187) | 18 uM | Abnormal | Children (1-13 years old) | Male | details |
Occipital Horn Syndrome (304150 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Copper (HMDB0000657) | 6.6 uM | Abnormal | Adult (>18 years old) | Male | details | |
| Copper (HMDB0000657) | 11.4 uM | Abnormal | Children (1-13 years old) | Male | details |
Dopamine Beta-Hydroxylase Deficiency (223360 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Dopamine (HMDB0000073) | >0.000650 uM | Abnormal | Adult (>18 years old) | Not Specified | details | |
| Norepinephrine (HMDB0000216) | <0.000150 uM | Abnormal | Adult (>18 years old) | Not Specified | details |