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| Term | peroxisome biogenesis disorder 7A | ID (Ontology) | DOID:0080482 (Human Disease) |
| Definition | A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX26 gene on chromosome 22q11. | ||
| Also Known As | "peroxisome biogenesis disorder 7A (Zellweger)" | ||
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| DO.org | |||
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autosomal recessive disease______ peroxisomal biogenesis disorder__| Zellweger syndrome |__peroxisome biogenesis disorder 7A |
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| Is a | Zellweger syndrome | ||
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| MIM:614872 | |||