|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of ALS with juvenile onset caused_by mutation located_in HNRNPA1 gene located_in chromosome 12. (Human Disease Ontology, DOID_0060211)|
|Downloads & Tools|
1 genes associated with the amyotrophic lateral sclerosis 20 phenotype from the curated OMIM Gene-Disease Associations dataset.
|HNRNPA1||heterogeneous nuclear ribonucleoprotein A1|