/amyotrophic lateral sclerosis type 12

amyotrophic lateral sclerosis type 12

Rare Disease

MONDO:0013264

Also Known As

ALS12OPTN amyotrophic lateral sclerosisamyotrophic lateral sclerosis 12amyotrophic lateral sclerosis 12 with or without frontotemporal dementiaamyotrophic lateral sclerosis caused by mutation in OPTNamyotrophic lateral sclerosis type 12

Definition

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

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Associated Genes

OPTN ↗

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

External Resources

OMIM

OMIM:613435 ↗

GARD

GARD:15663 ↗

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