Q189167

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Zellweger syndrome(Q189167)

rare congenital disorder characterized by the reduction or absence of functional peroxisomes in the cells of an individual
  • cerebrohepatorenal syndrome
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Language Label Description Also known as
English
Zellweger syndrome
rare congenital disorder characterized by the reduction or absence of functional peroxisomes in the cells of an individual
  • cerebrohepatorenal syndrome

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