FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
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Term autosomal recessive distal hereditary motor neuronopathy 9 ID (Ontology) DOID:0081428 (Human Disease)
Definition An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and atrophy, resulting in gait difficulties and that has_material_basis_in homozygous or compound heterozygous mutation in the COQ7 gene on chromosome 16p12.
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 autosomal recessive distal hereditary motor neuronopathy 9       1
 for disease ribbon | autosomal recessive distal hereditary motor neuronopathy 9       1
 model of | autosomal recessive distal hereditary motor neuronopathy 9       1
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autosomal recessive disease__
spinal muscular atrophy______|
                             autosomal recessive distal hereditary motor neuronopathy
                              |__autosomal recessive distal hereditary motor neuronopathy 9  1 rec.
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MIM:620402