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General Information
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| Term |
childhood spinal muscular atrophy |
ID (Ontology) |
DOID:0060160 (Human Disease) |
| Definition |
A spinal muscular atrophy that is associated with the survival of motor neuron protein in childhood and that has_material_basis_in variation in the SMN gene. |
| Also Known As |
"spinal muscular atrophies of childhood" ; "survival motor neuron spinal muscular atrophy" |
| Comment |
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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 | 65 | | 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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childhood spinal muscular atrophy | 66 | 28 | 1 | ameliorates | childhood spinal muscular atrophy | 15 | -- | -- | exacerbates | childhood spinal muscular atrophy | 11 | -- | -- | model of | childhood spinal muscular atrophy | 40 | -- | -- |
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Relationships