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Disease Ontology Browser
autosomal dominant nonsyndromic deafness 28 (DOID:0110557)
Alliance: disease page
Synonyms: autosomal dominant deafness 28; DFNA28
Alt IDs: OMIM:608641, ICD10CM:H90.3
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 GRHL2 gene on chromosome 8q22.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.17
The Jackson Laboratory