autosomal recessive nonsyndromic deafness 61

Summary

DOID:0110513 - autosomal recessive nonsyndromic deafness 61

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 SLC26A5 gene on chromosome 7q22.

Synonyms: autosomal recessive deafness 61, DFNB61

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

: slc26a5

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013471 - autosomal recessive nonsyndromic hearing loss 61

MONDO:0013471 - autosomal recessive nonsyndromic hearing loss 61

MIM:

MIM:613865 - DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61

MIM:613865 - DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61

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

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

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