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General Information
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| Term |
autosomal dominant nonsyndromic deafness 7 |
ID (Ontology) |
DOID:0110591 (Human Disease) |
| Definition |
An autosomal dominant nonsyndromic deafness that is characterized by progressive high-tone hearing loss and has_material_basis_in variation in the chromosome region 1q21-q23. |
| Also Known As |
"autosomal dominant deafness 7" ; "DFNA7" |
| 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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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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autosomal dominant nonsyndromic deafness 7 | 2 | for disease ribbon | autosomal dominant nonsyndromic deafness 7 | 2 | model of | autosomal dominant nonsyndromic deafness 7 | 2 |
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