FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term Peroxisome biogenesis disorder 10B ID (Ontology) DOID:0081440 (Human Disease)
Definition A peroxisomal biogenesis disorder that is characterized by the overlapping phenotypes of neonatal adrenoleukodystrophy and infantile Refsum disease and that has_material_basis_in compound heterozygous mutation in the PEX3 gene on chromosome 6q24.
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 Peroxisome biogenesis disorder 10B       1
 for disease ribbon | Peroxisome biogenesis disorder 10B       1
 model of | Peroxisome biogenesis disorder 10B       1
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autosomal genetic disease
 |__autosomal recessive disease______
peroxisomal disease                  |
 |__peroxisomal biogenesis disorder__|
                                     Peroxisome biogenesis disorder 10B  1 rec.
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Is a autosomal recessive disease
peroxisomal biogenesis disorder
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MIM:617370