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| Term | frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | ID (Ontology) | DOID:0111227 (Human Disease) | |||||||||||||||||||||||||||
| Definition | A frontotemporal dementia and/or amyotrophic lateral sclerosis that has_material_basis_in heterozygous mutation in CHMP2B on 3p11.2. | |||||||||||||||||||||||||||||
| Also Known As | "ALS17" ; "AMYOTROPHIC LATERAL SCLEROSIS" ; "AMYOTROPHIC LATERAL SCLEROSIS 17 (FORMERLY)" (for all, see Synonyms field below) | |||||||||||||||||||||||||||||
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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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dementia |__frontotemporal dementia________ motor neuron disease | |__amyotrophic lateral sclerosis__| brain disease | |__frontotemporal dementia________| frontotemporal dementia and/or amyotrophic lateral sclerosis 7 41 rec. |
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| Is a |
amyotrophic lateral sclerosis frontotemporal dementia |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:C579991 MIM:600795 |
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