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Disease Ontology Browser
metachromatic leukodystrophy (DOID:10581)
Alliance: disease page
Synonyms: arylsulfatase A deficiency; deficiency of cerebroside-sulfatase; MLD; Scholz cerebral sclerosis; sulfatide lipoidosis
Alt IDs: OMIM:249900, OMIM:250100, ICD10CM:E75.25, MESH:D007966, NCI:C61251, ORDO:512, UMLS_CUI:C0023522
Definition: A sphingolipidosis characterized by the accumulation of sulfatides in cells, especially the myelin producing cells of the nervous system.

Disease References using Mouse Models (3)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory