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| Term | autosomal recessive nonsyndromic deafness 1B | ID (Ontology) | DOID:0110476 (Human Disease) |
| Definition | An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12. | ||
| Also Known As | "autosomal recessive deafness 1B" ; "DFNB1B" | ||
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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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nonsyndromic deafness________ autosomal recessive disease__| autosomal recessive nonsyndromic deafness |__autosomal recessive nonsyndromic deafness 1B |
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| Is a | autosomal recessive nonsyndromic deafness | ||
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ICD10CM:H90.3 MIM:612645 |
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