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DOID:0110493 - autosomal recessive nonsyndromic deafness 35
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24.
Synonyms: autosomal recessive deafness 35, DFNB35
Xenbase Genes : esrrb
MONDO:0012060 - autosomal recessive nonsyndromic hearing loss 35 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee