amyotrophic lateral sclerosis and/or frontotemporal dementia Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in C9ORF72 gene located_in chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. (Human Disease Ontology, DOID_0060213)
External Link http://www.omim.org/entry/105550
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Genes

1 genes associated with the amyotrophic lateral sclerosis and/or frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
C9ORF72 chromosome 9 open reading frame 72