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 10 ID (Ontology) DOID:0060201 (Human Disease)
Definition An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1.
Also Known As "ALS10" ; "amyotrophic lateral sclerosis 10" ; "amyotrophic lateral sclerosis 10, with or without frontotemporal dementia" (for all, see Synonyms field below)
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS     319
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 amyotrophic lateral sclerosis type 10     333    173      1
 ameliorates | amyotrophic lateral sclerosis type 10     145       --       --
 exacerbates | amyotrophic lateral sclerosis type 10      87       --       --
 for disease ribbon | amyotrophic lateral sclerosis type 10       --       2       --
 model of | amyotrophic lateral sclerosis type 10     104      2       --
 DOES NOT exacerbate | amyotrophic lateral sclerosis type 10       4       --       --
 DOES NOT model | amyotrophic lateral sclerosis type 10       1       --       --
Spanning Tree (Parents/Children)
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  motor neuron disease
   |__amyotrophic lateral sclerosis
       |__amyotrophic lateral sclerosis type 10  507 rec.
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Is a amyotrophic lateral sclerosis
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Synonyms
  • "ALS10" EXACT OMO:0003012
    "amyotrophic lateral sclerosis 10" EXACT
    "amyotrophic lateral sclerosis 10, with or without frontotemporal dementia" EXACT
    "TARDBP-related frontotemporal lobar degeneration with TDP43 inclusions" EXACT
Secondary IDs
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GARD:10497
MIM:612069