/amyotrophic lateral sclerosis type 18

amyotrophic lateral sclerosis type 18

Rare Disease

MONDO:0013891

Also Known As

ALS18PFN1 amyotrophic lateral sclerosisamyotrophic lateral sclerosis 18amyotrophic lateral sclerosis caused by mutation in PFN1amyotrophic lateral sclerosis type 18

Definition

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the PFN1 gene.

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Comprehensive, easy-to-understand information about this condition

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Associated Genes

PFN1 ↗

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

External Resources

OMIM

OMIM:614808 ↗

GARD

GARD:15841 ↗

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