metachromatic leukodystrophy Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system. (Human Disease Ontology, DOID_10581)
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Genes

4 genes involed in the disease metachromatic leukodystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ARSA arylsulfatase A
ARSB arylsulfatase B
PSAP prosaposin
SUMF1 sulfatase modifying factor 1