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DOID:0110574 - autosomal dominant nonsyndromic deafness 4B
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.
Synonyms: DFNA4B, autosomal dominant deafness 4B,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee