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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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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05/28/2024
MGI 6.13 		The Jackson Laboratory