FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term autosomal dominant distal hereditary motor neuronopathy ID (Ontology) DOID:0111198 (Human Disease)
Definition A spinal muscular atrophy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration, and that has_material_basis_in autosomal dominant inheritance.
Also Known As "autosomal dominant dHMN" ; "autosomal dominant distal hereditary motor neuropathy" ; "autosomal dominant distal spinal muscular atrophy"
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Human Disease Models (FBhh)  DOID       1
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 autosomal dominant distal hereditary motor neuronopathy       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
motor neuron disease            |
 |__spinal muscular atrophy_____|
                                autosomal dominant distal hereditary motor neuronopathy  38 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 1
                                 |__autosomal dominant distal hereditary motor neuronopathy 2 15 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 3 6 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 4 13 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 5 2 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 6
                                 |__autosomal dominant distal hereditary motor neuronopathy 7 1 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 8 3 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 9 1 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 10
                                 |__autosomal dominant distal hereditary motor neuronopathy 11 1 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 12 1 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 13 1 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 14 3 rec.
                                 |__autosomal dominant distal hereditary motor neuronopathy 15 1 rec.
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Is a autosomal dominant disease
spinal muscular atrophy
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Synonyms
  • "autosomal dominant dHMN" EXACT
    "autosomal dominant distal hereditary motor neuropathy" EXACT
    "autosomal dominant distal spinal muscular atrophy" EXACT
Secondary IDs
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MIM:PS182960
ORDO:140465