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| Term | autosomal recessive nonsyndromic deafness 40 | ID (Ontology) | DOID:0110499 (Human Disease) |
| Definition | An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 22q11.21-q12.1. | ||
| Also Known As | "autosomal recessive deafness 40" ; "DFNB40" | ||
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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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No relevant statements available
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nonsyndromic deafness________ autosomal recessive disease__| autosomal recessive nonsyndromic deafness |__autosomal recessive nonsyndromic deafness 40 |
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| Is a | autosomal recessive nonsyndromic deafness | ||
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ICD10CM:H90.3 MIM:608264 |
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