(Q55345680)
(Redirected from Q66084896)
English
distal hereditary motor neuropathy type 1
autosomal dominant neurodegenerative disorder characterized by juvenile onset, distal motor weakness without sensory impairment, and anterior horn cell degeneration
- HMN1
- Charcot-Marie-Tooth Disease, Spinal, 1
- NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I
- Neuropathy, Distal Hereditary Motor, Type 1
- Autosomal dominant distal juvenile spinal muscular atrophy type 1
- Hmn 1
- Spinal Muscular Atrophy, Distal, Juvenile, Autosomal Dominant, 1
- Charcot-Marie-Tooth Disease, Spinal, I
- Distal Hereditary Motor Neuronopathy Type I
- NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I; HMN1
- dHMN1
- distal hereditary motor neuronopathy type 1
- autosomal dominant distal juvenile spinal muscular atrophy type 1
- distal hereditary motor neuropathy type I
- HMN I
- spinal Charcot-Marie-Tooth disease 1
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C132826
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