FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term peroxisome biogenesis disorder 6A ID (Ontology) DOID:0080481 (Human Disease)
Definition A Zellweger syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PEX10 gene on chromosome 1p36.
Also Known As "peroxisome biogenesis disorder 6A (Zellweger)"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 peroxisome biogenesis disorder 6A       1      1
 for disease ribbon | peroxisome biogenesis disorder 6A       1       --
 model of | peroxisome biogenesis disorder 6A       1       --
Spanning Tree (Parents/Children)
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autosomal recessive disease______
peroxisomal biogenesis disorder__|
                                 Zellweger syndrome
                                  |__peroxisome biogenesis disorder 6A  2 rec.
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Synonyms
  • "peroxisome biogenesis disorder 6A (Zellweger)" EXACT
Secondary IDs
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MIM:614870