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MeSH keywords -> Related genes, diseases (OMIM)


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01 Polycystic Kidney, Autosomal Recessive [NCBI]

Gene


 Gene Link Information
Gain		 01
PKHD1 [NCBI] 0.000626769
PKD1 [NCBI] 0.00010627
IFT88 [NCBI] 7.99953e-05
NPHP1 [NCBI] 5.15431e-05
EGF [NCBI] 2.78404e-05
NPHP3 [NCBI] 2.45245e-05
EGFR [NCBI] 2.3616e-05
TRAM2 [NCBI] 1.34667e-05
AREG [NCBI] 1.23319e-05
NEK8 [NCBI] 1.1985e-05
TMEM67 [NCBI] 1.04573e-05
TUBB [NCBI] 9.54055e-06
MCM3 [NCBI] 9.31893e-06
TUBB2A [NCBI] 8.86514e-06
CSNK2B [NCBI] 8.86514e-06
MUT [NCBI] 8.78722e-06
INVS [NCBI] 8.78722e-06
TFAP2B [NCBI] 8.3232e-06
GSTA1 [NCBI] 7.27331e-06
MTPN [NCBI] 7.09497e-06
NID1 [NCBI] 6.06896e-06
PAX2 [NCBI] 5.90785e-06
ADAM17 [NCBI] 4.62791e-06
HNF1B [NCBI] 4.1035e-06
BTK [NCBI] 4.03952e-06
CFTR [NCBI] 3.56874e-06
MYC [NCBI] 3.53389e-06
BRAF [NCBI] 2.96726e-06
PCNA [NCBI] 1.01633e-06



OMIM


 OMIM Link Information
gain		 01
polycystic kidneys [NCBI] 0.00213499
ARPKD [NCBI] 0.00206405
polycystic kidney disease, potter type i, with microbrachycephaly, hypertelorism, and brachymelia [NCBI] 0.00137383
campomelia, cumming type [NCBI] 0.00102023
PKHD1 [NCBI] 0.000901437
TTC10 [NCBI] 0.000187143
NPHP3 [NCBI] 0.000124516
NPHP1 [NCBI] 0.000120724
caroli disease, isolated [NCBI] 0.000119634
NPHP1 [NCBI] 0.000115097
renal dysplasia, diffuse cystic [NCBI] 9.71713e-05
NEK1 [NCBI] 8.86992e-05
EGF [NCBI] 8.72338e-05
MCM3 [NCBI] 8.11133e-05
TRAM2 [NCBI] 8.11133e-05
MKS3 [NCBI] 7.91149e-05
NPHP4 [NCBI] 7.91149e-05
PKD2 [NCBI] 7.6846e-05
NPHP2 [NCBI] 6.88211e-05
NPHP3 [NCBI] 6.88211e-05
mulibrey nanism [NCBI] 5.7198e-05
SLSN1 [NCBI] 5.31732e-05
TFAP2B [NCBI] 4.78301e-05
INVS [NCBI] 4.78301e-05
ADAM17 [NCBI] 4.61014e-05
EGFR [NCBI] 4.33586e-05
MKS1 [NCBI] 3.77789e-05
CFTR [NCBI] 2.00994e-05
PTK2 [NCBI] 1.14324e-05
PCNA [NCBI] 3.39448e-07



Database Center for Life Science