amyotrophic lateral sclerosis 7 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 20. (Human Disease Ontology, DOID_0060199)
External Link http://www.omim.org/entry/608031
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Genes

1 genes associated with the amyotrophic lateral sclerosis 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ALS7 amyotrophic lateral sclerosis 7