Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110557 - autosomal dominant nonsyndromic deafness 28


Disease Ontology 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.

Synonyms: DFNA28, autosomal dominant deafness 28

Xenbase Genes : grhl2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012083 - autosomal dominant nonsyndromic deafness 28

OMIM:
OMIM:608641 - DEAFNESS, AUTOSOMAL DOMINANT 28; DFNA28

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant nonsyndromic deafness (is_a)