autosomal recessive nonsyndromic deafness 36

Summary

DOID:0110494 - autosomal recessive nonsyndromic deafness 36

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36.

Synonyms: DFNB36, autosomal recessive deafness 36,

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

OMIM:

MIM:609006 - deafness, autosomal recessive 36, with or without vestibular involvement; dfnb36 deafness, autosomal dominant, without vestibular involvement, included

MIM:609006 - deafness, autosomal recessive 36, with or without vestibular involvement; dfnb36 deafness, autosomal dominant, without vestibular involvement, included

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)