autosomal recessive nonsyndromic deafness 59

Summary

DOID:0110511 - autosomal recessive nonsyndromic deafness 59

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the DFNB59 gene on chromosome 2q31.

Synonyms: DFNB59, autosomal recessive deafness 59

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

: pjvk

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012445 - autosomal recessive nonsyndromic hearing loss 59

MONDO:0012445 - autosomal recessive nonsyndromic hearing loss 59

MIM:

MIM:610220 - DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59

MIM:610220 - DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59

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

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

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