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DO Term : peroxisome biogenesis disorder 2A [DOID:0080477] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.
  • synonyms:
  • OMIM:214110,
  • peroxisome biogenesis disorder 2A (Zellweger),
  • 214110
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