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Genetics
HPS1 gene
Legg-Calvé-Perthes disease
CHN1 gene
Myotonic dystrophy
TGM3 gene
Unverricht-Lundborg disease
Atelosteogenesis type 2
Hepatic veno-occlusive disease with immunodeficiency
Narcolepsy
CLCN2-related leukoencephalopathy
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