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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 3B (DOID:0110565)
Synonyms: autosomal dominant deafness 3B; DFNA3B
Alt IDs: OMIM:612643, ICD10CM:H90.3, ORDO:90635
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.


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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
04/18/2017
MGI 6.08
The Jackson Laboratory