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autosomal dominant nonsyndromic deafness 3B (DOID:0110565)
Alliance: disease page
Synonyms: autosomal dominant deafness 3B; DFNA3B
Alt IDs: OMIM:612643, ICD10CM:H90.3
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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MGI 6.11
The Jackson Laboratory