About   Help   FAQ
Disease Ontology Browser
autosomal recessive nonsyndromic deafness 49 (DOID:0110506)
Synonyms: autosomal recessive deafness 49; DFNB49
Alt IDs: OMIM:610153, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, stable hearing loss and has_material_basis_in mutation in the MARVELD2 gene on chromosome 5q13.

Disease References using Mouse Models (1)
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
06/20/2017
MGI 6.10 		The Jackson Laboratory