About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 15 (DOID:0110470)
Alliance: disease page
Synonyms: autosomal recessive deafness 15; autosomal recessive deafness 72; autosomal recessive deafness 95; DFNB15; DFNB72; DFNB95
Alt IDs: OMIM:601869, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GIPC3 gene on chromosome 19p13.

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
11/19/2024
MGI 6.24 		The Jackson Laboratory