Amyotrophic lateral sclerosis type 20

Definition

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the HNRNPA1 gene.

Also known as ALS20, amyotrophic lateral sclerosis 20, amyotrophic lateral sclerosis caused by mutation in HNRNPA1, amyotrophic lateral sclerosis type 20, HNRNPA1 amyotrophic lateral sclerosis — per MONDO

Also identified as

• DOID 0060211 per MONDO
• OMIM 615426 per MONDO
• UMLS C3715156 per MONDO