/amyotrophic lateral sclerosis type 20

amyotrophic lateral sclerosis type 20

Rare Disease

MONDO:0014181

Also Known As

ALS20HNRNPA1 amyotrophic lateral sclerosisamyotrophic lateral sclerosis 20amyotrophic lateral sclerosis caused by mutation in HNRNPA1amyotrophic lateral sclerosis type 20

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

HNRNPA1 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:615426 ↗

GARD

GARD:15964 ↗

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