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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: autosomal recessive deafness 4 with enlarged vestibular aqueduct, DFNB4
Xenbase Genes : foxi1, slc26a4.3, kcnj10, slc26a4.1, slc26a4.2
MONDO:0010933 - autosomal recessive nonsyndromic hearing loss 4 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee