Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hearing Loss, High-Frequency [NCBI]

Gene


 Gene Link Information
Gain		 01
DFNA7 [NCBI] 0.000438875
KCNQ4 [NCBI] 5.7735e-05
GJB2 [NCBI] 3.68801e-05
DFNA5 [NCBI] 1.21782e-05
COCH [NCBI] 1.07746e-05
GJB3 [NCBI] 1.05435e-05
GJB6 [NCBI] 9.99351e-06
MS [NCBI] 7.68417e-06
NAT2 [NCBI] 7.05568e-06
GSTT1 [NCBI] 6.36966e-06
GSTM1 [NCBI] 6.04889e-06



OMIM


 OMIM Link Information
gain		 01
DFNA7 [NCBI] 0.00107364
deafness, progressive high-tone neural [NCBI] 0.000817902
FSHMD1A [NCBI] 0.000420804
GJB2 [NCBI] 0.000161879
DFNA5 [NCBI] 0.000107884
keratoderma, palmoplantar, with deafness [NCBI] 0.000105561
DFNA2 [NCBI] 0.000100104
AHC [NCBI] 8.23123e-05
EVA [NCBI] 8.03786e-05
DFNA5 [NCBI] 7.00104e-05
osteogenesis imperfecta, type i [NCBI] 6.63736e-05
KCNQ4 [NCBI] 6.6175e-05
GJB3 [NCBI] 5.99015e-05
RA [NCBI] 9.48154e-08



Database Center for Life Science