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Summary Literature (0)
DOID:0060214 - frontotemporal dementia and/or amyotrophic lateral sclerosis 2

Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.

Synonyms: frontotemporal dementia and/or amyotrophic lateral sclerosis 2, FTDALS2

Xenbase Genes : chchd10

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014395 - frontotemporal dementia and/or amyotrophic lateral sclerosis 2


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)