Browsing Serum Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 465 - 468 of 479 in total
Molybdenium co-factor deficiency (252150 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Sulfite (HMDB0000240) | 500 umol/mmol creatinine | Abnormal | Infant (0-1 year old) | Female | details | |
| Xanthine (HMDB0000292) | 48 umol/mmol creatinine | Abnormal | Infant (0-1 year old) | Female | details | |
| Xanthine (HMDB0000292) | 259 umol/mmol creatinine | Abnormal | Children (1-13 years old) | Male | details | |
| Uracil (HMDB0000300) | 48 umol/mmol creatinine | Abnormal | Children (1-13 years old) | Male | details | |
| Uric acid (HMDB0000289) | 29 umol/mmol creatinine | Abnormal | Infant (0-1 year old) | Female | details |
Glutamine deficiency, congenital (610015 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Glutamine (HMDB0000641) | 0-8 umol/mmol creatinine | Abnormal | Newborn (0-30 days old) | Both | details |
Mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma (609313 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Copper (HMDB0000657) | 0.17 umol/mmol creatinine | Abnormal | Children (1-13 years old) | Male | details |
Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type (250940 )
| Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
|---|