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| Term | C9orf72 frontotemporal dementia and/or amyotrophic lateral sclerosis | ID (Ontology) | DOID:0060213 (Human Disease) | |||||||||||||||||||||||||||
| Definition | An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis. | |||||||||||||||||||||||||||||
| Also Known As | "ALSFTD" ; "amyotrophic lateral sclerosis and/or frontotemporal dementia" ; "C9orf72-FTD/ALS" (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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motor neuron disease |__amyotrophic lateral sclerosis |__C9orf72 frontotemporal dementia and/or amyotrophic lateral sclerosis 599 rec. |
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| Is a | amyotrophic lateral sclerosis | ||
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External Crossreferences & Linkouts
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| MIM:105550 | |||