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DOID:0110561 - autosomal dominant nonsyndromic deafness 31
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p21.3.
Synonyms: DFNA31, autosomal dominant deafness 31,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee