About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 86 (DOID:0110532)
Alliance: disease page
Synonyms: autosomal recessive deafness 86; DFNB86
Alt IDs: OMIM:614617, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory