Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Gingival Hyperplasia	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	5.28348e-05
EGF	[NCBI]	2.0368e-05
CYP2C19	[NCBI]	1.68596e-05
ERC2	[NCBI]	1.47485e-05
WNT5A	[NCBI]	9.25769e-06
PCNA	[NCBI]	9.22603e-06
BMP4	[NCBI]	7.58938e-06
FGF7	[NCBI]	7.58185e-06
CYP2C9	[NCBI]	7.135e-06
IL1A	[NCBI]	6.8781e-06
EGR1	[NCBI]	6.78158e-06
IL4	[NCBI]	6.40466e-06
CTSL1	[NCBI]	6.22332e-06
ABCB1	[NCBI]	6.18994e-06
IL8	[NCBI]	6.17023e-06
BMP2	[NCBI]	6.05047e-06
IL1B	[NCBI]	5.50705e-06
CD68	[NCBI]	4.49225e-06
TGFB1	[NCBI]	3.85559e-06

OMIM	Link	Information gain
ZLS	[NCBI]	0.00229642
hypertrichosis universalis	[NCBI]	0.00161608
broad terminal phalanges, familial	[NCBI]	0.00109818
fibromatosis, gingival, with progressive deafness	[NCBI]	0.000880362
HTC2	[NCBI]	0.000705355
HTC1	[NCBI]	0.000605677
neutropenia, chronic familial	[NCBI]	0.000545541
fibromatosis, gingival, with hypertrichosis	[NCBI]	0.000542911
robinow syndrome, autosomal dominant	[NCBI]	0.000484704
focal epithelial hyperplasia, oral	[NCBI]	0.000111796
RNS	[NCBI]	9.11242e-05
GINGF	[NCBI]	9.11242e-05
EGF	[NCBI]	8.62678e-05
PDP	[NCBI]	8.31153e-05
mannosidosis, alpha b, lysosomal	[NCBI]	7.37888e-05
ABCB1	[NCBI]	4.3553e-05
PCNA	[NCBI]	3.60647e-05
FGF7	[NCBI]	3.45198e-05
SPP1	[NCBI]	2.46539e-05
RA	[NCBI]	2.27258e-06