mynachat

G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

乳児型脊髄性筋萎縮症,Ⅰ型[ウェルドニッヒ・ホフマン<Werdnig-Hoffman>病]

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Spinal muscular atrophy (SMA)
指定難病 #3. Disease self-declared, backed by certification or disease-specific drugs
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Proof: Prescription proxy, 指定難病 certification (coming soon), Medical subsidy certificate (PMH) (coming soon), Diagnosis record (EHR) (coming soon)