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autosomal dominant nonsyndromic deafness 56 (DOID:0110581)
Alliance: disease page
Synonyms: autosomal dominant deafness 56; DFNA56
Alt IDs: OMIM:615629, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33.


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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
12/05/2017
MGI 6.11
The Jackson Laboratory