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Summary Literature (0)
DOID:1927 - sphingolipidosis

Disease Ontology Definition:A lipid storage disease characterized by functional deficiencies in the enzymes needed for lysosomal degradation of sphingolipid substrates.

Synonyms: sphingolipidoses, Sphingolipidosis, Sphingolipidosis (disorder), Sphingolipidosis, NOS

Xenbase Genes : sumf1, apoe, npc1, smpd1, gm2a, galc, glb1, hexb, psap, gla, arsa.2, arsa, npc2, gba1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019255 - lower eyelash


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): lipid storage disease (is_a)