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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 6 (DOID:0110512)
Alliance: disease page
Synonyms: autosomal recessive deafness 6; DFNB6
Alt IDs: OMIM:600971, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TMIE gene on chromosome 3p21.


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
11/12/2019
MGI 6.14
The Jackson Laboratory