RDX, radixin, 5962

N. diseases: 80; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.310 GeneticVariation phenotype LHGDN Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus. 17226784 2007
CUI: C1384666
Disease: hearing impairment
hearing impairment
0.310 Biomarker phenotype GENOMICS_ENGLAND Molecular cloning, cDNA sequence, and chromosomal assignment of the human radixin gene and two dispersed pseudogenes. 8486357 1993