has material basis in germline mutation in CHCHD10 familial amyotrophic lateral sclerosis frontotemporal dementia and/or amyotrophic lateral sclerosis 2 https://www.malacards.org/card/frontotemporal_dementia_and_or_amyotrophic_lateral_sclerosis_2 frontotemporal dementia and/or amyotrophic lateral sclerosis type 2 UMLS:C4014648 MEDGEN:863085 MONDO:0014395 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. DOID:0060214 OMIM:615911 FTDALS2 frontotemporal dementia and/or amyotrophic lateral sclerosis 2 GARD:0018397 frontotemporal dementia with motor neuron disease frontotemporal dementia and/or amyotrophic lateral sclerosis