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DOID:0110553 - autosomal dominant nonsyndromic deafness 23
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the SIX1 gene on chromosome 14q23.
Synonyms: autosomal dominant deafness 23, DFNA23
Xenbase Genes : six1
MONDO:0011519 - autosomal dominant nonsyndromic hearing loss 23 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee