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MeSH keywords -> Related genes, diseases (OMIM)


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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