Ontological Term Details

Metabolite
HMDB0015532 (Zinc)
Term
Metachromatic Leukodystrophy (MLD)
Definition
a defect in this enzyme results in accumulation of 3-o-sulfogalactosylceramide in urine, neural and non neural tisues like kidney and gallbladder. there are several forms of mld.
Parent Term
Biochemical pathway
Parent Definition
A linked series of chemical reactions that occur in a defined order within or between organism cells, and lead to a known function or end product.
Other Metabolites Mapped to 'Metachromatic Leukodystrophy (MLD)'
  • HMDB0000024 (3-O-Sulfogalactosylceramide (d18:1/24:0))
  • HMDB0000061 (Adenosine 3',5'-diphosphate)
  • HMDB0000122 (D-Glucose)
  • HMDB0000140 (Glucosylceramide)
  • HMDB0000143 (D-Galactose)
  • HMDB0000187 (L-Serine)
  • HMDB0000217 (NADP)
  • HMDB0000221 (NADPH)
  • HMDB0000224 (O-Phosphoethanolamine)
  • HMDB0000252 (Sphingosine)

    • References