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autosomal dominant nonsyndromic deafness 2A (DOID:0110558)
Synonyms: autosomal dominant deafness 2A; DFNA2A
Alt IDs: OMIM:600101, ICD10CM:H90.3, ORDO:90635
Definition: An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2.


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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
03/21/2017
MGI 6.08
The Jackson Laboratory