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DOID:0110474 - autosomal recessive nonsyndromic deafness 18B
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15.
Synonyms: DFNB18B, autosomal recessive deafness 18B,
Xenbase Genes : otog
MONDO:0013985 - autosomal recessive nonsyndromic hearing loss 18B |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee