Browsing Serum Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 437 - 440 of 479 in total
Molybdenium co-factor deficiency (252150 )
Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
---|---|---|---|---|---|---|
Xanthine (HMDB0000292) | 18 uM | Abnormal | Infant (0-1 year old) | Female | details | |
Uric acid (HMDB0000289) | 23 uM | Abnormal | Infant (0-1 year old) | Female | details | |
Homocysteine (HMDB0000742) | 0.9 uM | Abnormal | Children (1-13 years old) | Male | details |
Monocarboxylate transporter 1 deficiency (616095 )
Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
---|---|---|---|---|---|---|
Hydrogen carbonate (HMDB0000595) | 5000-15000 uM | Abnormal | Children (1-13 years old) | Male | details |
Myoclonic epilepsy and ragged red fiber disease (545000 )
Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
---|---|---|---|---|---|---|
Lactic acid (HMDB0000190) | 1820.646-5273.214 uM | Abnormal | Adult (>18 years old) | Both | details |
Myopathic carnitine deficiency (212160 )
Metabolite | Concentration in Serum | Patient Status | Age | Sex | Reference | Details |
---|---|---|---|---|---|---|
L-Carnitine (HMDB0000062) | 20.6-33.8 uM | Abnormal | Adult (>18 years old) | Female | details |