amyotrophic lateral sclerosis 20 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS with juvenile onset caused_by mutation located_in HNRNPA1 gene located_in chromosome 12. (Human Disease Ontology, DOID_0060211)
External Link http://www.omim.org/entry/615426
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Genes

1 genes associated with the amyotrophic lateral sclerosis 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
HNRNPA1 heterogeneous nuclear ribonucleoprotein A1