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:0111227 - frontotemporal dementia and/or amyotrophic lateral sclerosis 7


Disease Ontology Definition:A frontotemporal dementia and/or amyotrophic lateral sclerosis that has_material_basis_in heterozygous mutation in CHMP2B on 3p11.2.

Synonyms: ALS17 (FORMERLY), AMYOTROPHIC LATERAL SCLEROSIS, AMYOTROPHIC LATERAL SCLEROSIS 17 (FORMERLY), CHMP2B-RELATED, CHMP2B-related frontotemporal dementia, FRONTOTEMPORAL DEMENTIA, FTD3, FTDALS7, amyotrophic lateral sclerosis type 17, chromosome 3-linked frontotemporal dementia,

Xenbase Genes : chmp2b



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): frontotemporal dementia (is_a)