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DOID:0110525 - autosomal recessive nonsyndromic deafness 77
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21.
Synonyms: DFNB77, autosomal recessive deafness 77,
Echinobase Genes :
MIM:613079 - deafness, autosomal recessive 77; dfnb77 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee