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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: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