autosomal dominant nonsyndromic deafness 10

Summary

DOID:0110542 - autosomal dominant nonsyndromic deafness 10

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.

Synonyms: DFNA10, autosomal dominant deafness 10,

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

: eya4

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011031 - autosomal dominant nonsyndromic hearing loss 10

MONDO:0011031 - autosomal dominant nonsyndromic hearing loss 10

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)