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DOID:0110476 - autosomal recessive nonsyndromic deafness 1B
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.
Synonyms: DFNB1B, autosomal recessive deafness 1B,
Xenbase Genes :
MONDO:0012977 - autosomal recessive nonsyndromic hearing loss 1B |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee