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autosomal dominant nonsyndromic deafness 41 (DOID:0110567)
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Synonyms: autosomal dominant deafness 41; DFNA41
Alt IDs: OMIM:608224, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in mutation in the P2RX2 gene on chromosome 12q24.

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The Jackson Laboratory