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autosomal recessive nonsyndromic deafness 76 (DOID:0110524)
Alliance: disease page
Synonyms: autosomal recessive deafness 76; DFNB76
Alt IDs: OMIM:615540, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has_material_basis_in mutation in the SYNE4 gene on chromosome 19q13.


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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
12/13/2017
MGI 6.11
The Jackson Laboratory