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 (0)
DOID:0111130 - focal segmental glomerulosclerosis 5

Disease Ontology Definition:A focal segmental glomerulosclerosis that has_material_basis_in an autosomal dominant mutation of the INF2 gene on chromosome 14q32.33.

Synonyms: FSGS5

Xenbase Genes : inf2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013191 - focal segmental glomerulosclerosis 5

MIM:
MIM:613237 - FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5; FSGS5

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), focal segmental glomerulosclerosis (is_a)