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 2 ID (Ontology) DOID:0060194 (Human Disease)
Definition An amyotrophic lateral sclerosis that has_material_basis_in mutation in the alsin gene on chromosome 2.
Also Known As "ALS2" ; "amyotrophic lateral sclerosis 2" ; "amyotrophic lateral sclerosis 2, juvenile"
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DO.org
Annotations
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       6
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 amyotrophic lateral sclerosis type 2       6      5      1
 ameliorates | amyotrophic lateral sclerosis type 2       2       --       --
 exacerbates | amyotrophic lateral sclerosis type 2       2       --       --
 for disease ribbon | amyotrophic lateral sclerosis type 2       --       1       --
 model of | amyotrophic lateral sclerosis type 2       2      1       --
Spanning Tree (Parents/Children)
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  motor neuron disease
   |__amyotrophic lateral sclerosis
       |__amyotrophic lateral sclerosis type 2  12 rec.
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Is a amyotrophic lateral sclerosis
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Synonyms
  • "ALS2" EXACT OMO:0003012
    "amyotrophic lateral sclerosis 2" EXACT
    "amyotrophic lateral sclerosis 2, juvenile" EXACT
Secondary IDs
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GARD:9470
ICD10CM:G12.2
MIM:205100