|
DOID:0110515 - autosomal recessive nonsyndromic deafness 63
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 LRTOMT gene on chromosome 11q13.
Synonyms: autosomal recessive deafness 63, DFNB63
Xenbase Genes : lrtomt
MONDO:0012670 - autosomal recessive nonsyndromic hearing loss 63 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee