Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Placenta Diseases	[NCBI]

Gene	Link	Information Gain
PIH	[NCBI]	3.65676e-05
TFPI2	[NCBI]	1.59965e-05
AFP	[NCBI]	1.57846e-05
VEGFA	[NCBI]	1.55801e-05
SOCS3	[NCBI]	1.37577e-05
FLT1	[NCBI]	1.28865e-05
SLC38A1	[NCBI]	1.22318e-05
HSPA6	[NCBI]	1.13527e-05
SLC2A1	[NCBI]	1.11466e-05
HSD3B1	[NCBI]	1.04753e-05
IL1RAP	[NCBI]	9.99877e-06
PRDX3	[NCBI]	9.39216e-06
C5AR1	[NCBI]	8.59115e-06
SOCS2	[NCBI]	8.50215e-06
LHCGR	[NCBI]	8.50215e-06
SLC2A3	[NCBI]	7.74434e-06
CXCL13	[NCBI]	7.48675e-06
HSPA1A	[NCBI]	7.4396e-06
CD68	[NCBI]	7.2942e-06
INHBA	[NCBI]	7.26309e-06
SERPINA3	[NCBI]	7.24226e-06
PTX3	[NCBI]	7.1614e-06
ICAM3	[NCBI]	7.01041e-06
NOS2	[NCBI]	6.89422e-06
HDC	[NCBI]	6.4343e-06
FCGR2A	[NCBI]	6.10825e-06
SOCS1	[NCBI]	5.96621e-06
CDKN1C	[NCBI]	5.89946e-06
SLC11A1	[NCBI]	4.94919e-06
ADRB2	[NCBI]	4.94392e-06
CASP3	[NCBI]	4.75039e-06
ALK	[NCBI]	4.64196e-06
TF	[NCBI]	4.47172e-06
IFNG	[NCBI]	4.38349e-06
IL4	[NCBI]	4.35757e-06
ADAMTS13	[NCBI]	4.16068e-06
TLR2	[NCBI]	3.99409e-06
PGR	[NCBI]	3.96506e-06
SHBG	[NCBI]	3.81949e-06
ESR1	[NCBI]	3.61552e-06
IL10	[NCBI]	3.15641e-06
TLR4	[NCBI]	2.9095e-06
NOS3	[NCBI]	2.52788e-06
TNF	[NCBI]	1.95399e-06
BAX	[NCBI]	1.89458e-06
PTGS2	[NCBI]	1.02322e-06
EGF	[NCBI]	9.18821e-07

OMIM	Link	Information gain
AOS	[NCBI]	0.00063536
SRS	[NCBI]	0.000460245
BWS	[NCBI]	0.00034601
camptomelic syndrome, long-limb type	[NCBI]	0.000107702
PROCR	[NCBI]	9.81163e-05
chondrodysplasia punctata, autosomal dominant	[NCBI]	8.76406e-05
RTD	[NCBI]	8.31153e-05
ichthyosis, x-linked	[NCBI]	8.10157e-05
epidermolysis bullosa with pyloric atresia	[NCBI]	7.89629e-05
NR2F2	[NCBI]	6.48439e-05
AFP	[NCBI]	6.16904e-05
PTX3	[NCBI]	4.67926e-05
PXE	[NCBI]	4.43005e-05
SOCS3	[NCBI]	4.30105e-05
HDC	[NCBI]	2.93332e-05
CYP1A1	[NCBI]	2.49146e-05
hla-d histocompatibility type	[NCBI]	2.43067e-05
PGR	[NCBI]	1.74257e-05
SHBG	[NCBI]	1.42566e-05
F3	[NCBI]	9.96453e-06
VEGF	[NCBI]	9.94544e-06
TNF	[NCBI]	3.26796e-06
CEACAM5	[NCBI]	8.69133e-07
EGF	[NCBI]	6.90229e-07