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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 1B (DOID:0110476)
Synonyms: autosomal recessive deafness 1B; DFNB1B
Alt IDs: OMIM:612645, ICD10CM:H90.3, ORDO:90636
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and 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
03/14/2017
MGI 6.08
The Jackson Laboratory