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| Term | Alzheimer's disease 1 | ID (Ontology) | DOID:0080348 (Human Disease) | |||||||||||||||||||||||||||||||||||
| Definition | An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21. | |||||||||||||||||||||||||||||||||||||
| Also Known As | "Alzheimer's disease 1, early onset" | |||||||||||||||||||||||||||||||||||||
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autosomal genetic disease |__autosomal dominant disease__ tauopathy | |__Alzheimer's disease_________| Alzheimer's disease 1 588 rec. |
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autosomal dominant disease Alzheimer's disease |
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External Crossreferences & Linkouts
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| MIM:104300 | |||