U.S. flag

An official website of the United States government

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

12 tests are in the database for this condition.

Clinical tests (12 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

Help
Imported from Human Phenotype Ontology (HPO)

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.