Rare – Page 377 – CheckOrphan

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Page 377

Myalgia eosinophilia associated with tryptophan

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Myasthenic syndrome- congenital- associated with acetylcholine receptor deficiency

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Myasthenic syndrome- congenital- slow-channel

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Muscular fibrosis multifocal obstructed vessels

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Hereditary carnitine deficiency

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Infantile convulsions and paroxysmal choreoathetosis- familial

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Infantile digital fibromatosis

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Myasthenia gravis

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Myasthenia gravis

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Myasthenia- familial

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