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autosomal dominant nonsyndromic deafness 31 (DOID:0110561)
Alliance: disease page
Synonyms: autosomal dominant deafness 31; DFNA31
Alt IDs: OMIM:608645, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p21.3.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory