Browsing CSF Metabolite Diseases and Conditions
Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 141 - 144 of 172 in total
Coenzyme Q10 deficiency, primary, 1 (607426 )
| Metabolite | Concentration in CSF | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 11767.592 uM | Abnormal | Infant (0-1 year old) | Male | details |
Myoclonic epilepsy and ragged red fiber disease (545000 )
| Metabolite | Concentration in CSF | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 2109.285-6527.683 uM | Abnormal | Adult (>18 years old) | Both | details |
Carnitine transporter defect; primary systemic carnitine deficiency (212140 )
| Metabolite | Concentration in CSF | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| D-Glucose (HMDB0000122) | 200 uM | Abnormal | Infant (0-1 year old) | Female | details | |
| alpha-D-Glucose (HMDB0003345) | 200 uM | Abnormal | Infant (0-1 year old) | Female | details |
Coenzyme Q10 deficiency
| Metabolite | Concentration in CSF | Patient Status | Age | Sex | Reference | Details |
|---|---|---|---|---|---|---|
| Lactic acid (HMDB0000190) | 4000 uM | Abnormal | Children (1-13 years old) | Male | details |