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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 48 (DOID:0110571)
Synonyms: autosomal dominant deafness 48; DFNA48
Alt IDs: OMIM:607841, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14.


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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
06/20/2017
MGI 6.10
The Jackson Laboratory