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General Information
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| Term |
nemaline myopathy 7 |
ID (Ontology) |
DOID:0110934 (Human Disease) |
| Definition |
A nemaline myopathy characterized by very early onset of hypotonia and delayed motor development that has_material_basis_in homozygous mutation in the CFL2 gene on chromosome 14q13. |
| Also Known As |
"NEM7" ; "nemaline myopathy 7, autosomal recessive" |
| 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 | 6 | | 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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nemaline myopathy 7 | 6 | 4 | 1 | ameliorates | nemaline myopathy 7 | 1 | -- | -- | exacerbates | nemaline myopathy 7 | 1 | -- | -- | for disease ribbon | nemaline myopathy 7 | -- | 2 | -- | model of | nemaline myopathy 7 | 4 | 2 | -- |
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Relationships