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DOID:0110508 - autosomal recessive nonsyndromic deafness 51
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 11p13-p12.
Synonyms: DFNB51, autosomal recessive deafness 51,
Xenbase Genes :
MONDO:0012370 - autosomal recessive nonsyndromic hearing loss 51 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee