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| Term | autosomal dominant nonsyndromic deafness 41 | ID (Ontology) | DOID:0110567 (Human Disease) |
| Definition | An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the purinergic receptor P2X 2 gene (P2RX2) on chromosome 12q24. | ||
| Also Known As | "autosomal dominant deafness 41" ; "DFNA41" | ||
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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 dominant disease__| autosomal dominant nonsyndromic deafness |__autosomal dominant nonsyndromic deafness 41 |
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| Is a | autosomal dominant nonsyndromic deafness | ||
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ICD10CM:H90.3 MIM:608224 |
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