(Q2362826)

English

Werdnig–Hoffmann disease

Human disease

  • Werdnig–Hoffmann syndrome
  • Werdnig-Hoffmann disease
  • infantile muscular atrophy
  • progressive muscular atrophy of infancy
  • Werdnig-Hoffman disease
  • spinal muscular atrophy type 1
  • HMN (Hereditary motor Neuropathy) Proximal type I
  • hereditary motor neuropathy proximal type I
  • Spinal muscular atrophy 1
  • SMA1

Statements

Identifiers

 
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