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Echinobase
Summary Literature (0)
DOID:0060214 - FTDALS2

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,

Echinobase Genes :


OMIM:
MIM:615911 - frontotemporal dementia and/or amyotrophic lateral sclerosis 2; ftdals2

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

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