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General Information
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| Term |
amyotrophic lateral sclerosis type 22 |
ID (Ontology) |
DOID:0060355 (Human Disease) |
| Definition |
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TUBA4A gene on chromosome 2q35. |
| Also Known As |
"ALS22" ; "amyotrohpic lateral sclerosis 22 with or without frontotemporal dementia" ; "amyotrophic lateral sclerosis 22" |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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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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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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amyotrophic lateral sclerosis type 22 | 5 | for disease ribbon | amyotrophic lateral sclerosis type 22 | 5 | model of | amyotrophic lateral sclerosis type 22 | 5 |
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