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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: autosomal recessive deafness 37, DFNB37
Xenbase Genes : myo6
MONDO:0011912 - autosomal recessive nonsyndromic hearing loss 37 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee