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MeSH keywords -> Related genes, diseases (OMIM)


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01 Hernia [NCBI]

Gene


 Gene Link Information
Gain		 01
IL28RA [NCBI] 1.84648e-05
INSL3 [NCBI] 1.31975e-05



OMIM


 OMIM Link Information
gain		 01
chiari malformation type i [NCBI] 0.000925375
megarbane syndrome [NCBI] 0.000154415
plantar lipomatosis, unusual facies, and developmental delay [NCBI] 0.000131943
carpenter syndrome [NCBI] 0.000107884
young syndrome [NCBI] 0.000107884
robinow syndrome, autosomal recessive [NCBI] 8.84935e-05
INSL3 [NCBI] 8.55726e-05
ehlers-danlos syndrome, type i [NCBI] 7.94923e-05
CF [NCBI] 3.44722e-06



Database Center for Life Science