About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 9 (DOID:0110535)
Alliance: disease page
Synonyms: autosomal recessive deafness 9; DFNB9; neurosensory nonsyndromic recessive deafness 9; NRSD9
Alt IDs: OMIM:601071, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23.

Disease References using Mouse Models (2)
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
11/12/2024
MGI 6.24 		The Jackson Laboratory