Amyotrophic Lateral Sclerosis 20

Preferred Label : Amyotrophic Lateral Sclerosis 20;

NCIt synonyms : ALS20;

NCIt definition : An autosomal dominant form of amyotrophic lateral sclerosis caused by mutation(s) in the HNRNPA1 gene, encoding heterogeneous nuclear ribonucleoprotein A1.;

Détails

Origin ID

C214858;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- HNRNPA1 Gene [NCIt concept]

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