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DOID:3659 - sialuria
Disease Ontology Definition:A lysosomal storage disease characterized by increased sialic acid in the urine.
Synonyms:
Echinobase Genes

MIM:269921 - sialuria |
MIM:604369 - salla disease; sd |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
lysosomal storage disease (is_a)