About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 30 (DOID:0110489)
Alliance: disease page
Synonyms: autosomal recessive deafness 30; DFNB30
Alt IDs: OMIM:607101, ICD10CM:H90.3, ORDO:90636
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1.

Disease References using Mouse Models (1)
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
11/05/2024
MGI 6.24 		The Jackson Laboratory