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| Term | amyotrophic lateral sclerosis type 3 | ID (Ontology) | DOID:0060195 (Human Disease) |
| Definition | An amyotrophic lateral sclerosis that has_material_basis_in mutation in loci on chromosome 18. | ||
| Also Known As | "ALS3" ; "amyotrophic lateral sclerosis 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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motor neuron disease |__amyotrophic lateral sclerosis |__amyotrophic lateral sclerosis type 3 |
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| Is a | amyotrophic lateral sclerosis | ||
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GARD:10501 MIM:606640 |
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