FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term amyotrophic lateral sclerosis type 20 ID (Ontology) DOID:0060211 (Human Disease)
Definition An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the HNRNPA1 gene on chromosome 12.
Also Known As "ALS20" ; "amyotrophic lateral sclerosis 20"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 amyotrophic lateral sclerosis type 20       4      1
 for disease ribbon | amyotrophic lateral sclerosis type 20       4       --
 model of | amyotrophic lateral sclerosis type 20       4       --
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  motor neuron disease
   |__amyotrophic lateral sclerosis
       |__amyotrophic lateral sclerosis type 20  5 rec.
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Is a amyotrophic lateral sclerosis
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Synonyms
  • "ALS20" EXACT OMO:0003012
    "amyotrophic lateral sclerosis 20" EXACT
Secondary IDs
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MIM:615426