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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 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)