Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Polycystic Kidney, Autosomal Recessive	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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