Portal:RareDisease/FeaturedPathways

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MECP2 and Associated Rett Syndrome (Homo sapiens)
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Amyotrophic lateral sclerosis (ALS) (Homo sapiens)
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Fanconi Anemia Pathway (Homo sapiens)
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The effect of progerin on the involved genes in Hutchinson-Gilford Progeria Syndrome (Homo sapiens)
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Lamin A-processing pathway (Homo sapiens)
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Viral Acute Myocarditis (Homo sapiens)

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