Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in CHCHD10 gene located_in chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. (Human Disease Ontology, DOID_0060214)
External Link http://www.omim.org/entry/615911
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Genes

1 genes associated with the Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CHCHD10 coiled-coil-helix-coiled-coil-helix domain containing 10