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DOID:0110484 - autosomal recessive nonsyndromic deafness 26
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 4q31.
Synonyms: autosomal recessive deafness 26, DFNB26
Xenbase Genes :
MONDO:0011553 - autosomal recessive nonsyndromic hearing loss 26 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee