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 26 ID (Ontology) DOID:0081380 (Human Disease)
Definition An amyotrophic lateral sclerosis that is characterized by adult onset of upper and low motor neuron disease causing bulbar dysfunction and limb weakness and that has_material_basis_in heterozygous mutation in the TIA1 gene on chromosome 2p13.
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 amyotrophic lateral sclerosis type 26       3
 for disease ribbon | amyotrophic lateral sclerosis type 26       3
 model of | amyotrophic lateral sclerosis type 26       3
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autosomal genetic disease
 |__autosomal dominant disease_____
motor neuron disease               |
 |__amyotrophic lateral sclerosis__|
                                   amyotrophic lateral sclerosis type 26  3 rec.
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Is a autosomal dominant disease
amyotrophic lateral sclerosis
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MIM:619133