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DOID:0110507 - autosomal recessive nonsyndromic deafness 5
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 14q12.
Synonyms: DFNB5, autosomal recessive deafness 5,
Xenbase Genes :
MONDO:0000912 - autosomal recessive nonsyndromic hearing loss 5 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee