About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 91 (DOID:0110536)
Alliance: disease page
Synonyms: autosomal recessive deafness 91; DFNB91
Alt IDs: OMIM:613453, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SERPINB6 gene on chromosome 6p25.


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