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DOID:0110514 - autosomal recessive nonsyndromic deafness 62
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 12p13.2-p11.23.
Synonyms: autosomal recessive deafness 62, DFNB62
Xenbase Genes :
MONDO:0012418 - autosomal recessive nonsyndromic hearing loss 62 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee