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Summary Literature (0)
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 : eya4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011031 - autosomal dominant nonsyndromic deafness 10

OMIM:
OMIM:601316 - DEAFNESS, AUTOSOMAL DOMINANT 10; DFNA10

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)