autosomal dominant nonsyndromic deafness 11

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Summary

Literature (0)

DOID:0110543 - autosomal dominant nonsyndromic deafness 11

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Synonyms: DFNA11, autosomal dominant deafness 11,

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

: myo7a

OMIM:

MIM:601317 - deafness, autosomal dominant 11; dfna11

MIM:601317 - deafness, autosomal dominant 11; dfna11

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)