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 6 ID (Ontology) DOID:0060198 (Human Disease)
Definition An amyotrophic lateral sclerosis that has_material_basis_in mutation in the FUS gene on chromosome 16.
Also Known As "ALS6" ; "amyotrophic lateral sclerosis 6, with or without frontotemporal dementia" ; "autosomal recessive amyotrophic lateral sclerosis 6"
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS     162
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 amyotrophic lateral sclerosis type 6     174     72      1
 ameliorates | amyotrophic lateral sclerosis type 6      79       --       --
 exacerbates | amyotrophic lateral sclerosis type 6      36       --       --
 for disease ribbon | amyotrophic lateral sclerosis type 6       --       1       --
 model of | amyotrophic lateral sclerosis type 6      62      1       --
 DOES NOT ameliorate | amyotrophic lateral sclerosis type 6       3       --       --
 DOES NOT exacerbate | amyotrophic lateral sclerosis type 6       3       --       --
 DOES NOT model | amyotrophic lateral sclerosis type 6       2       --       --
Spanning Tree (Parents/Children)
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  motor neuron disease
   |__amyotrophic lateral sclerosis
       |__amyotrophic lateral sclerosis type 6  247 rec.
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Is a amyotrophic lateral sclerosis
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Synonyms
  • "ALS6" EXACT OMO:0003012
    "amyotrophic lateral sclerosis 6, with or without frontotemporal dementia" EXACT
    "autosomal recessive amyotrophic lateral sclerosis 6" EXACT
Secondary IDs
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GARD:9874
MIM:608030