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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: DFNB35, autosomal recessive deafness 35
OMIM:608565 - DEAFNESS, AUTOSOMAL RECESSIVE 35; DFNB35 |
MONDO:0012060 - autosomal recessive nonsyndromic deafness 35 |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD