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DOID:0110532 - autosomal recessive nonsyndromic deafness 86
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13.
Synonyms: DFNB86, autosomal recessive deafness 86,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0013826 - autosomal recessive nonsyndromic hearing loss 86 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee