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| Term | Pearson syndrome | ID (Ontology) | DOID:0060067 (Human Disease) |
| Definition | A mitochondrial metabolism disease that is characterized by sideroblastic anemia and exocrine pancreas dysfunction. | ||
| Also Known As | "Pearson Marrow-Pancreas Syndrome" | ||
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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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inherited metabolic disorder |__mitochondrial metabolism disease |__Pearson syndrome |
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| Is a | mitochondrial metabolism disease | ||
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External Crossreferences & Linkouts
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GARD:7343 MIM:557000 |
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