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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 21 (DOID:0110551)
Synonyms: autosomal dominant deafness 21; DFNA21
Alt IDs: OMIM:607017, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p24.1-p22.3.


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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