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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 49 (DOID:0110572)
Synonyms: autosomal dominant deafness 49; DFNA49
Alt IDs: OMIM:608372, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has_material_basis_in variation in the chromosome region 1q21-q23.


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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
05/16/2017
MGI 6.09
The Jackson Laboratory