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autosomal dominant nonsyndromic deafness 41 (DOID:0110567)
Alliance: disease page
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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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory