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Disease Ontology Browser
autosomal recessive nonsyndromic deafness 22 (DOID:0110480)
Synonyms: autosomal recessive deafness 22; DFNB22
Alt IDs: OMIM:607039, 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 mutation in the OTOA gene on chromosome 16p12.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory