|
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: DFNB3, NRSD3, autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3,
Echinobase Genes :
MIM:600316 - deafness, autosomal recessive 3; dfnb3 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee