metachromatic leukodystrophy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/250100
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Genes

1 genes associated with the metachromatic leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ARSA arylsulfatase A