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DOID:0110569 - autosomal dominant nonsyndromic deafness 44
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has_material_basis_in mutation in the CCDC50 gene on chromosome 3q28.
Synonyms: DFNA44, autosomal dominant deafness 44,
Echinobase Genes :
MIM:607453 - deafness, autosomal dominant 44; dfna44 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee