Werdnig–Hoffmann disease (Q2362826)
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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
Language | Label | Description | Also known as |
---|---|---|---|
English | Werdnig–Hoffmann disease |
Human disease |
|
Statements
1 reference
Identifiers
Maladie de Werdnig-Hoffmann
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(4 entries)
- frwiki Maladie de Werdnig-Hoffmann
- itwiki Malattia di Werdnig-Hoffmann
- jawiki ウエルドニッヒ・ホフマン症
- plwiki Zespół Werdniga-Hoffmanna