FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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Term autosomal dominant distal hereditary motor neuronopathy 11 ID (Ontology) DOID:0081400 (Human Disease)
Definition An autosomal dominant distal hereditary motor neuronopathy that is characterized by juvenile or young-adult onset of distal limb muscle weakness and atrophy mainly affecting the lower limbs, resulting in gait instability and walking difficulties and that has_material_basis_in heterozygous mutation in the SPTAN1 gene on chromosome 9q34.
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 autosomal dominant distal hereditary motor neuronopathy 11       1
 for disease ribbon | autosomal dominant distal hereditary motor neuronopathy 11       1
 model of | autosomal dominant distal hereditary motor neuronopathy 11       1
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autosomal dominant disease__
spinal muscular atrophy_____|
                            autosomal dominant distal hereditary motor neuronopathy
                             |__autosomal dominant distal hereditary motor neuronopathy 11  1 rec.
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MIM:620528