Amyotrophic lateral sclerosis 20 Gene Set

Dataset ClinVar Gene-Phenotype 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)
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1 genes associated with the Amyotrophic lateral sclerosis 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
HNRNPA1 heterogeneous nuclear ribonucleoprotein A1