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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 36 (DOID:0110563)
Synonyms: autosomal dominant deafness 36; DFNA36
Alt IDs: OMIM:606705, ICD10CM:H90.3, ORDO:90635
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.

Disease References using Mouse Models (3)

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
04/18/2017
MGI 6.08
The Jackson Laboratory