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DOID:0110566 - autosomal dominant nonsyndromic deafness 40
Disease Ontology Definition:An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12.
Synonyms: DFNA40, autosomal dominant deafness 40,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0014603 - autosomal dominant nonsyndromic hearing loss 40 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee