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| Term | amyotrophic lateral sclerosis type 1 | ID (Ontology) | DOID:0060193 (Human Disease) | |||||||||||||||||||||||||||
| Definition | An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. | |||||||||||||||||||||||||||||
| Also Known As | "ALS1" ; "amyotrophic lateral sclerosis 1" | |||||||||||||||||||||||||||||
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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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autosomal genetic disease |__autosomal dominant disease_____ |__autosomal recessive disease____| motor neuron disease | |__amyotrophic lateral sclerosis__| amyotrophic lateral sclerosis type 1 40 rec. |
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| Is a |
autosomal dominant disease autosomal recessive disease amyotrophic lateral sclerosis |
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External Crossreferences & Linkouts
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ICD10CM:G12.2 MIM:105400 |
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