amyotrophic lateral sclerosis 3 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS with loci associated with the disease located_in chromosome 18. (Human Disease Ontology, DOID_0060195)
External Link http://www.omim.org/entry/606640
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Genes

1 genes associated with the amyotrophic lateral sclerosis 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ALS3 amyotrophic lateral sclerosis 3 (autosomal dominant)