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DOID:0110467 - autosomal recessive nonsyndromic deafness 12
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 CDH23 gene on chromosome 10q22.
Synonyms: autosomal recessive deafness 12, DFNB12
Xenbase Genes : cdh23
MONDO:0011067 - autosomal recessive nonsyndromic hearing loss 12 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee