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DOID:0110498 - autosomal recessive nonsyndromic deafness 4
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SLC26A4 gene on chromosome 7q22.
Synonyms: DFNB4, autosomal recessive deafness 4 with enlarged vestibular aqueduct,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:600791 - deafness, autosomal recessive 4, with enlarged vestibular aqueduct; dfnb4 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee