autosomal recessive nonsyndromic deafness 35

Summary

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,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: esrrb

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012060 - autosomal recessive nonsyndromic hearing loss 35

MONDO:0012060 - autosomal recessive nonsyndromic hearing loss 35

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)