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| Term | peroxisome biogenesis disorder 2B | ID (Ontology) | DOID:0080622 (Human Disease) |
| Definition | A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease______ peroxisomal disease | |__peroxisomal biogenesis disorder__| peroxisome biogenesis disorder 2B 1 rec. |
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| Is a |
autosomal recessive disease peroxisomal biogenesis disorder |
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External Crossreferences & Linkouts
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| MIM:202370 | |||