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Summary Literature (0)
DOID:0060213 - frontotemporal dementia and/or amyotrophic lateral sclerosis 1

Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.

Synonyms: ALSFTD, amyotrophic lateral sclerosis and/or frontotemporal dementia, frontotemporal dementia and/or amyotrophic lateral sclerosis 1, frontotemporal dementia and/or motor neuron disease, FTDALS1, FTDMND

Xenbase Genes : c1h9orf72

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007105 - frontotemporal dementia and/or amyotrophic lateral sclerosis 1


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)