autosomal recessive nonsyndromic deafness 30

Summary

DOID:0110489 - autosomal recessive nonsyndromic deafness 30

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 mutations in the MYO3A gene on chromosome 10p12.1.

Synonyms: autosomal recessive deafness 30, DFNB30

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

: myo3a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011774 - autosomal recessive nonsyndromic hearing loss 30

MONDO:0011774 - autosomal recessive nonsyndromic hearing loss 30

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)