autosomal recessive nonsyndromic deafness 3

Summary

DOID:0110488 - autosomal recessive nonsyndromic deafness 3

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 MYO15A gene on chromosome 17p11.

Synonyms: autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3, DFNB3, NRSD3

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

: myo15a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010860 - autosomal recessive nonsyndromic hearing loss 3

MONDO:0010860 - autosomal recessive nonsyndromic hearing loss 3

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)