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General Information
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| Term |
amyotrophic lateral sclerosis type 25 |
ID (Ontology) |
DOID:0081379 (Human Disease) |
| Definition |
An amyotrophic lateral sclerosis that is characterized by rapidly progressive muscle weakness and death due to respiratory failure and that has_material_basis_in heterozygous mutation in the KIF5A gene on chromosome 12q13. ALS25 may have a lower median age at onset (46.5 years) and longer median survival (10 years) than that found in epidemiologic studies (62.5 years and 20 to 30 months, respectively). |
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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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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 2 | | Human Disease Models (FBhh) | DOID | 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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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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amyotrophic lateral sclerosis type 25 | 3 | 2 | 1 | for disease ribbon | amyotrophic lateral sclerosis type 25 | -- | 1 | -- | model of | amyotrophic lateral sclerosis type 25 | 2 | 1 | -- | DOES NOT model | amyotrophic lateral sclerosis type 25 | 1 | -- | -- |
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Relationships