About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 66 (DOID:0110517)
Alliance: disease page
Synonyms: autosomal recessive deafness 66; DFNB66
Alt IDs: OMIM:610212, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the DCDC2 gene on chromosome 6p22.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
11/14/2017
MGI 6.11
The Jackson Laboratory