autosomal dominant nonsyndromic deafness 12

Summary

DOID:0110544 - autosomal dominant nonsyndromic deafness 12

Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.

Synonyms: autosomal dominant deafness 12, autosomal dominant deafness 8, DFNA12, DFNA8

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

: tecta.2, tecta

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011102 - autosomal dominant nonsyndromic hearing loss 12

MONDO:0011102 - autosomal dominant nonsyndromic hearing loss 12

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant nonsyndromic deafness (is_a)