autosomal dominant nonsyndromic deafness 28

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: grhl2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012083 - autosomal dominant nonsyndromic hearing loss 28

MONDO:0012083 - autosomal dominant nonsyndromic hearing loss 28

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)