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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 9 (DOID:0110593)
Synonyms: autosomal dominant deafness 9; DFNA9
Alt IDs: OMIM:601369, ICD10CM:H90.3, ORDO:90635
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.08
The Jackson Laboratory