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amyotrophic lateral sclerosis type 10

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

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

Synonyms

  • ALS10
  • Ftld-TDP, Tardbp-related
  • TARDBP amyotrophic lateral sclerosis
  • TARDBP-related frontotemporal lobar degeneration with Tdp43 inclusions
  • amyotrophic lateral sclerosis 10
  • amyotrophic lateral sclerosis 10 with or without frontotemporal dementia
  • amyotrophic lateral sclerosis 10, with or without FTD
  • amyotrophic lateral sclerosis 10, with or without frontotemporal dementia
  • amyotrophic lateral sclerosis caused by mutation in TARDBP
  • amyotrophic lateral sclerosis type 10
  • frontotemporal dementia with Tdp43 inclusions, Tardbp-related
  • frontotemporal lobar Degeneration with Tdp43 inclusions, Tardbp-related
  • frontotemporal lobar degeneration, TARDBP-related
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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