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