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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 8 (DOID:0110527)
Alliance: disease page
Synonyms: autosomal recessive deafness 8; autosomal recessive deafness 10; childhood-onset neurosensory autosomal recessive deafness 8; DFNB8; DFNB10; neurosensory nonsyndromic recessive deafness 8; NRSD8
Alt IDs: OMIM:601072, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22.


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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
06/12/2024
MGI 6.13
The Jackson Laboratory