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

Xenbase Genes : chmp2b


MIM:
MIM:600795 - FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 7; FTDALS7

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

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