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GTR Home > Conditions/Phenotypes > Amyotrophic lateral sclerosis type 20

Amyotrophic lateral sclerosis type 20

Summary

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

Available tests

15 tests are in the database for this condition.

Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, MPD3, UP 1, hnRNP A1, hnRNP-A1, HNRNPA1
    Summary: heterogeneous nuclear ribonucleoprotein A1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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