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DOID:0110503 - autosomal recessive nonsyndromic deafness 46
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 18p11.32-p11.31.
Synonyms: DFNB46, autosomal recessive deafness 46,
Xenbase Genes :
MONDO:0012327 - autosomal recessive nonsyndromic hearing loss 46 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee