Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Genital Diseases, Female [NCBI]

Gene


 Gene Link Information
Gain		 01
KTWS [NCBI] 0.000332969
SNAPC3 [NCBI] 1.51199e-05
PRL [NCBI] 1.27446e-05
IFNGR1 [NCBI] 1.23594e-05
TNF [NCBI] 1.14697e-05
RPS27 [NCBI] 1.07742e-05
ACTN1 [NCBI] 1.06839e-05
GNRH1 [NCBI] 1.05981e-05
FERMT1 [NCBI] 1.02922e-05
NUMA1 [NCBI] 9.51686e-06
CXADR [NCBI] 9.15668e-06
EZR [NCBI] 9.12097e-06
CSF1 [NCBI] 9.12097e-06
FSHR [NCBI] 8.82923e-06
GNRHR [NCBI] 8.714e-06
SOX2 [NCBI] 8.55452e-06
DSP [NCBI] 7.85618e-06
SPINT2 [NCBI] 7.5486e-06
CRH [NCBI] 7.11613e-06
IGF2 [NCBI] 6.28737e-06
IGFBP3 [NCBI] 6.17117e-06
CCR5 [NCBI] 5.39984e-06
IGF1 [NCBI] 5.29316e-06
IL8 [NCBI] 5.07562e-06
COMT [NCBI] 4.91247e-06
SHBG [NCBI] 4.76137e-06
CCL2 [NCBI] 4.48195e-06
PLAUR [NCBI] 4.02921e-06
IL6 [NCBI] 3.55517e-06
VEGFA [NCBI] 2.52952e-06
PCNA [NCBI] 2.388e-06
CDKN1A [NCBI] 2.00851e-06
PTGS2 [NCBI] 1.79987e-06



OMIM


 OMIM Link Information
gain		 01
behcet syndrome [NCBI] 0.00134595
genitopatellar syndrome [NCBI] 0.000938013
SPINK1 [NCBI] 0.000113182
temporal arteritis [NCBI] 0.000102955
severe combined immunodeficiency with sensitivity to ionizing radiation [NCBI] 9.37927e-05
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 7.09823e-05
BBS [NCBI] 5.97522e-05
CEACAM5 [NCBI] 5.90893e-05
RNASE3 [NCBI] 3.41471e-05
PRL [NCBI] 3.16783e-05
TLR2 [NCBI] 2.8201e-05
TNF [NCBI] 2.22962e-05
NF1 [NCBI] 1.94363e-05
COMT [NCBI] 1.81981e-05
SHBG [NCBI] 1.34952e-05
SLE [NCBI] 1.11711e-05
VEGF [NCBI] 8.36857e-06
PCNA [NCBI] 2.48051e-06



Database Center for Life Science