Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Foot Diseases	[NCBI]

Gene	Link	Information Gain
MS	[NCBI]	5.28348e-05
MPO	[NCBI]	2.3692e-05
COMP	[NCBI]	1.77329e-05
NFKBIZ	[NCBI]	1.37725e-05
EGF	[NCBI]	1.30458e-05
SPTLC1	[NCBI]	1.16878e-05
PEBP1	[NCBI]	9.93078e-06
XDH	[NCBI]	9.54474e-06
EDA	[NCBI]	8.76754e-06
VIM	[NCBI]	8.40396e-06
PGF	[NCBI]	6.79584e-06
BMP2	[NCBI]	5.85624e-06
HFE	[NCBI]	4.47637e-06
CD68	[NCBI]	4.30149e-06
PCNA	[NCBI]	3.23024e-06
PTH	[NCBI]	2.61129e-06

OMIM	Link	Information gain
polydactyly, preaxial iii	[NCBI]	0.00111789
keratosis, focal palmoplantar and gingival	[NCBI]	0.000724991
keratosis palmoplantaris papulosa	[NCBI]	0.000693453
MSSE	[NCBI]	0.000644828
osteolysis, hereditary, of carpal bones with nephropathy	[NCBI]	0.000553054
lymphedema, microcephaly, chorioretinopathy syndrome	[NCBI]	0.000531565
thrombocytopenia-absent radius syndrome	[NCBI]	0.000426926
EEC1	[NCBI]	0.000408031
plantar lipomatosis, unusual facies, and developmental delay	[NCBI]	0.000254219
HSAN1	[NCBI]	0.000237787
lymphedema and cerebral arteriovenous anomaly	[NCBI]	0.000126878
DFSP	[NCBI]	0.000123031
peripheral dysostosis	[NCBI]	9.59359e-05
acrogeria, gottron type	[NCBI]	9.0434e-05
knuckle pads, leukonychia, and sensorineural deafness	[NCBI]	8.63444e-05
HMS	[NCBI]	7.80613e-05
CCT4	[NCBI]	7.59186e-05
lymphedema, hereditary, ii	[NCBI]	7.42375e-05
MPO	[NCBI]	7.29202e-05
COMP	[NCBI]	6.9978e-05
lymphedema, hereditary, i	[NCBI]	6.98047e-05
SYM1	[NCBI]	6.85628e-05
enchondromatosis, multiple	[NCBI]	6.53278e-05
erythermalgia, primary	[NCBI]	6.438e-05
HSAN2	[NCBI]	6.438e-05
PALS	[NCBI]	6.18336e-05
SPTLC1	[NCBI]	5.84987e-05
ODDD	[NCBI]	5.30269e-05
VIM	[NCBI]	3.64761e-05
EV	[NCBI]	3.00445e-05
EGF	[NCBI]	2.89816e-05
RA	[NCBI]	2.70372e-05
SLOS	[NCBI]	2.46012e-05
XDH	[NCBI]	2.04648e-05
PTHLH	[NCBI]	1.84787e-05
MUC1	[NCBI]	1.48546e-05
temporal arteritis	[NCBI]	1.40851e-05
PD	[NCBI]	6.79756e-06
VEGF	[NCBI]	4.67255e-06
PCNA	[NCBI]	4.55026e-06
SLE	[NCBI]	4.15703e-06
PTH	[NCBI]	2.22846e-06
CEACAM5	[NCBI]	1.95849e-06