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Summary Literature (0)
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

In OMIM:
OMIM:608565 - DEAFNESS, AUTOSOMAL RECESSIVE 35; DFNB35

In Mondo Disease Ontology:
MONDO:0012060 - autosomal recessive nonsyndromic deafness 35

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : esrrb

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive nonsyndromic deafness (is_a)