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DOID:0110519 - autosomal recessive nonsyndromic deafness 68
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13.
Synonyms: DFNB68, autosomal recessive deafness 68,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0012485 - autosomal recessive nonsyndromic hearing loss 68 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee