Clicking on any metabolite link will take you to the Human Metabolome Database.
Displaying diseases 153 - 156 of 172 in total
Leber Optic Atrophy and Dystonia  (500001 )
MetaboliteConcentration in CSFPatient StatusAgeSexReferenceDetails
Lactic acid (HMDB0000190) 3700 uMAbnormalAdult (>18 years old)Female details
Leigh Syndrome, French Canadian Type  (220111 )
MetaboliteConcentration in CSFPatient StatusAgeSexReferenceDetails
Lactic acid (HMDB0000190) 3600-6200 uMAbnormalAdolescent (13-18 years old)Both details
Lipoyltransferase 1 Deficiency  (616299 )
MetaboliteConcentration in CSFPatient StatusAgeSexReferenceDetails
Lactic acid (HMDB0000190) 6600 uMAbnormalChildren (1-13 years old)Male details
Pyruvic acid (HMDB0000243) 360 uMAbnormalChildren (1-13 years old)Male details
Glycine (HMDB0000123) 5 uMAbnormalChildren (1-13 years old)Male details
Glutamic acid (HMDB0000148) 0 uMAbnormalChildren (1-13 years old)Male details
L-Alanine (HMDB0000161) 52 uMAbnormalChildren (1-13 years old)Male details
Glutamine (HMDB0000641) 723 uMAbnormalChildren (1-13 years old)Male details
Myopathy, lactic acidosis, and sideroblastic anemia 1  (600462 )
MetaboliteConcentration in CSFPatient StatusAgeSexReferenceDetails
Lactic acid (HMDB0000190) 6000 uMAbnormalNewborn (0-30 days old)Male details
Lactic acid (HMDB0000190) 4400-5400 uMAbnormalInfant (0-1 year old)Both details
Displaying diseases 153 - 156 of 172 in total