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autosomal recessive nonsyndromic deafness 46 (DOID:0110503)
Alliance: disease page
Synonyms: autosomal recessive deafness 46; DFNB46
Alt IDs: OMIM:609647, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 18p11.32-p11.31.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory