Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (2)
DOID:1062 - Fanconi syndrome

Disease Ontology Definition:A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting.

Synonyms: Congenital Fanconi syndrome, Congenital Fanconi syndrome (disorder), De Toni-Fanconi syndrome, Fanconi-de Toni syndrome, Fanconi-de-Toni syndrome, Infantile nephropathic cystinosis, Lignac-Fanconi syndrome, adult Fanconi Anemia, adult Fanconi syndrome, deToni Fanconi syndrome,

Xenbase Genes : hnf4a, ehhadh

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0001083 - Fanconi renotubular syndrome


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): renal tubular transport disease (is_a)