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Summary Literature (0)
DOID:3659 - sialuria

Disease Ontology Definition:A lysosomal storage disease characterized by increased sialic acid in the urine.

Synonyms:

Xenbase Genes : slc17a5, gne

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010028 - ventral part of pharyngeal pouch 4

MIM:
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)