autosomal recessive nonsyndromic deafness 37

Summary

DOID:0110495 - autosomal recessive nonsyndromic deafness 37

Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.

Synonyms: DFNB37, autosomal recessive deafness 37,

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

: myo6

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011912 - autosomal recessive nonsyndromic hearing loss 37

MONDO:0011912 - autosomal recessive nonsyndromic hearing loss 37

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)