Browsing Urine Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 253 - 256 of 277 in total
Glutamine deficiency, congenital (610015 )
| Metabolite | Concentration in Urine | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Glutamine (HMDB0000641) | 0-8 umol/mmol creatinine | Abnormal | Newborn (0-30 days old) | Both | details |
Carnitine transporter defect; primary systemic carnitine deficiency (212140 )
| Metabolite | Concentration in Urine | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| L-Carnitine (HMDB0000062) | 1.517 umol/mmol creatinine | Abnormal | Children (1-13 years old) | Not Available | details |
Mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma (609313 )
| Metabolite | Concentration in Urine | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Copper (HMDB0000657) | 0.17 umol/mmol creatinine | Abnormal | Children (1-13 years old) | Male | details |
Myopathic carnitine deficiency (212160 )
| Metabolite | Concentration in Urine | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| L-Carnitine (HMDB0000062) | 9.395-121.200 umol/mmol creatinine | Abnormal | Adult (>18 years old) | Female | details |