|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the metachromatic leukodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.