autosomal recessive nonsyndromic deafness 79

Summary

DOID:0110526 - autosomal recessive nonsyndromic deafness 79

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 TPRN gene on chromosome 9q34.

Synonyms: DFNB79, autosomal recessive deafness 79,

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

: tprn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013215 - autosomal recessive nonsyndromic hearing loss 79

MONDO:0013215 - autosomal recessive nonsyndromic hearing loss 79

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)