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DOID:0110549 - autosomal dominant nonsyndromic deafness 18
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 3q22.
Synonyms: DFNA18, autosomal dominant deafness 18,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0011625 - autosomal dominant nonsyndromic hearing loss 18 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee