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DOID:0110536 - autosomal recessive nonsyndromic deafness 91
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SERPINB6 gene on chromosome 6p25.
Synonyms: DFNB91, autosomal recessive deafness 91,
Xenbase Genes : serpinb6
MONDO:0013269 - autosomal recessive nonsyndromic hearing loss 91 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee