Rare – Page 158 – CheckOrphan

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Powell Chandra Saal syndrome

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Powell Buist Stenzel syndrome

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Congenital disorder of glycosylation type 1B

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Battaglia Neri syndrome

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Congenital disorder of glycosylation type 1A

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Heterotaxy with polysplenia or asplenia

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Hillig syndrome

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Basal ganglia calcification- idiopathic 2

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Basal ganglia disease- biotin-responsive

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Usher syndrome- type 1E

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