Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Labyrinth Diseases [NCBI]

Gene


 Gene Link Information
Gain		 01
KCNQ4 [NCBI] 1.28049e-05
COCH [NCBI] 1.18861e-05
FGF3 [NCBI] 1.04858e-05
FADD [NCBI] 9.53458e-06
CLU [NCBI] 8.91562e-06
VIP [NCBI] 7.01568e-06
TH [NCBI] 6.54814e-06



OMIM


 OMIM Link Information
gain		 01
preauricular fistulae, congenital [NCBI] 0.00115589
deafness, progressive high-tone neural [NCBI] 0.000900049
deafness, sensorineural, with pituitary dwarfism [NCBI] 0.000152091
deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy [NCBI] 0.00012962
cochleosaccular degeneration of the inner ear with progressive cataracts [NCBI] 0.000121139
deafness, neural, with atypical atopic dermatitis [NCBI] 0.000111537
DFNA5 [NCBI] 0.000105561
deafness, aminoglycoside-induced [NCBI] 0.000101208
PHEX [NCBI] 6.39723e-05
VHL [NCBI] 5.73262e-05
VIP [NCBI] 3.11445e-05
TH [NCBI] 2.82172e-05
RA [NCBI] 5.50387e-07



Database Center for Life Science