MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Dilatation, Pathologic
[NCBI]
Gene
Gene
Link
Information
Gain
01
VUR
[NCBI]
0.00224853
ZLS
[NCBI]
0.000231894
MS
[NCBI]
0.000148802
GER
[NCBI]
6.12649e-05
CST3
[NCBI]
1.77001e-05
ACE
[NCBI]
1.6283e-05
PPBPL1
[NCBI]
1.47753e-05
TGFBR1
[NCBI]
1.2958e-05
MMP9
[NCBI]
1.16433e-05
KERA
[NCBI]
1.03395e-05
VIP
[NCBI]
9.82372e-06
VPS13A
[NCBI]
9.74976e-06
LAMB1
[NCBI]
9.74976e-06
LAMC1
[NCBI]
9.21791e-06
CD68
[NCBI]
8.51539e-06
BEST1
[NCBI]
7.86745e-06
ITGAM
[NCBI]
7.72814e-06
TGFBR2
[NCBI]
7.67176e-06
PTPRC
[NCBI]
7.65337e-06
SELP
[NCBI]
7.5643e-06
FBN1
[NCBI]
7.19173e-06
NPPB
[NCBI]
6.94561e-06
CNN1
[NCBI]
6.85179e-06
CKAP4
[NCBI]
5.77535e-06
NOS1
[NCBI]
5.7046e-06
PTPN11
[NCBI]
5.44823e-06
PF4
[NCBI]
5.32425e-06
PRKCB
[NCBI]
5.29691e-06
GJB1
[NCBI]
5.18337e-06
MMP2
[NCBI]
5.00737e-06
MUC1
[NCBI]
4.73845e-06
GJB2
[NCBI]
4.37341e-06
HLA-DQB1
[NCBI]
4.1038e-06
CCK
[NCBI]
3.5293e-06
HLA-DRB1
[NCBI]
3.49933e-06
TH
[NCBI]
3.2888e-06
PTEN
[NCBI]
3.02784e-06
NOS2
[NCBI]
2.90456e-06
TGFB1
[NCBI]
2.4933e-06
AR
[NCBI]
2.40063e-06
NGF
[NCBI]
2.32105e-06
VEGFA
[NCBI]
2.2202e-06
PCNA
[NCBI]
2.08206e-06
APOE
[NCBI]
2.01829e-06
CFTR
[NCBI]
1.87636e-06
PTGS2
[NCBI]
1.51242e-06
OMIM
OMIM
Link
Information
gain
01
aortic valve disease
[NCBI]
0.00130742
lateral meningocele syndrome
[NCBI]
0.000724991
ZLS
[NCBI]
0.000578037
intestinal atresia, multiple
[NCBI]
0.00056504
megacystis-microcolon-intestinal hypoperistalsis syndrome
[NCBI]
0.000553054
MYP2
[NCBI]
0.000541934
schinzel-giedion midface-retraction syndrome
[NCBI]
0.000521852
megaduodenum and/or megacystis
[NCBI]
0.000521852
aneurysm, intracranial berry, 1
[NCBI]
0.000412535
MFS
[NCBI]
0.000402987
CMTC
[NCBI]
0.00026538
aortic aneurysm, abdominal
[NCBI]
0.000209171
infundibulopelvic dysgenesis
[NCBI]
0.000120847
adrenomyodystrophy
[NCBI]
0.000120847
mydriasis, congenital
[NCBI]
0.000120847
rombo syndrome
[NCBI]
9.83832e-05
ELK3
[NCBI]
7.53661e-05
vacterl association with hydrocephalus
[NCBI]
7.20503e-05
lujan-fryns syndrome
[NCBI]
7.20503e-05
ehlers-danlos syndrome, type iii
[NCBI]
7.00279e-05
ehlers-danlos syndrome, type ii
[NCBI]
6.51514e-05
RA
[NCBI]
6.14826e-05
KTCN1
[NCBI]
5.58605e-05
SEMA3A
[NCBI]
5.58467e-05
hyperglycerolemia
[NCBI]
5.11628e-05
EVA
[NCBI]
4.70975e-05
EGR1
[NCBI]
4.66604e-05
ehlers-danlos syndrome, type i
[NCBI]
4.62276e-05
VIP
[NCBI]
3.75554e-05
osteogenesis imperfecta, type i
[NCBI]
3.34946e-05
FBN1
[NCBI]
3.27485e-05
PKD1
[NCBI]
3.21357e-05
NS1
[NCBI]
3.12957e-05
PTEN
[NCBI]
3.06452e-05
CD
[NCBI]
2.85864e-05
CF
[NCBI]
2.39761e-05
fragile x mental retardation syndrome
[NCBI]
2.34401e-05
NF1
[NCBI]
2.20955e-05
PF4
[NCBI]
2.13637e-05
PXE
[NCBI]
1.86474e-05
SPP1
[NCBI]
1.61362e-05
TNFRSF11B
[NCBI]
1.61064e-05
polycystic kidneys
[NCBI]
1.17602e-05
CCK
[NCBI]
1.10405e-05
CFTR
[NCBI]
1.09153e-05
TH
[NCBI]
9.66432e-06
CRH
[NCBI]
8.66483e-06
SLE
[NCBI]
8.44278e-06
APOE
[NCBI]
6.31248e-06
CD
[NCBI]
5.3716e-06
NGFB
[NCBI]
5.12288e-06
PCNA
[NCBI]
4.17995e-06
VEGF
[NCBI]
4.07482e-06
Database Center for Life Science