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:0110068 - frontotemporal dementia and/or amyotrophic lateral sclerosis 3

Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SQSTM1 gene on chromosome 5q35.

Synonyms: frontotemporal dementia and/or amyotrophic lateral sclerosis 3, FTDALS3

Xenbase Genes : sqstm1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014640 - frontotemporal dementia and/or amyotrophic lateral sclerosis 3


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): amyotrophic lateral sclerosis (is_a)