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amyotrophic lateral sclerosis type 21 | RareConnect | RareConnect.io

/familial amyotrophic lateral sclerosis

/amyotrophic lateral sclerosis type 21

amyotrophic lateral sclerosis type 21

Rare Disease

MONDO:0011632

Also Known As

ALS21MATR3 amyotrophic lateral sclerosisamyotrophic lateral sclerosis caused by mutation in MATR3amyotrophic lateral sclerosis type 21amyotrophic lateral sclerosis 21myopathy, distal, 2myopathy, distal, 2, formerlyvocal cord and pharyngeal dysfunction with distal myopathyvocal cord and pharyngeal dysfunction with distal myopathy, formerly

Definition

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the MATR3 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

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

External Resources

OMIM

OMIM:606070 ↗

GARD

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