Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Thrombocytopenia [NCBI]


Gene


Gene Link Information
Gain
01
MPL [NCBI] 0.000655434
PF4 [NCBI] 0.000653181
MYH9 [NCBI] 0.000555455
GHS [NCBI] 0.000389986
WAS [NCBI] 0.000375842
VWF [NCBI] 0.000250202
KTWS [NCBI] 0.000223418
ADAMTS13 [NCBI] 0.000182838
GATA1 [NCBI] 0.000155862
NEWENTRY [NCBI] 0.000131464
THPO [NCBI] 9.803e-05
ITGB3 [NCBI] 7.24737e-05
ZFPM1 [NCBI] 5.57821e-05
GP1BA [NCBI] 5.46711e-05
RUNX1 [NCBI] 4.70572e-05
MSLN [NCBI] 4.61577e-05
EPO [NCBI] 3.60356e-05
HOXA11 [NCBI] 3.39259e-05
MASTL [NCBI] 3.3846e-05
GP9 [NCBI] 3.20561e-05
ZNF85 [NCBI] 3.19313e-05
IL11 [NCBI] 3.00835e-05
ITGA2B [NCBI] 2.77437e-05
PPBP [NCBI] 2.73111e-05
TROVE2 [NCBI] 2.45143e-05
TPMT [NCBI] 2.28422e-05
NFE2 [NCBI] 2.00132e-05
JAK2 [NCBI] 1.90344e-05
FLI1 [NCBI] 1.84884e-05
FCGR2A [NCBI] 1.82974e-05
LIF [NCBI] 1.73658e-05
CD36 [NCBI] 1.58915e-05
CD109 [NCBI] 1.52895e-05
IL11RA [NCBI] 1.18146e-05
SCN4B [NCBI] 1.01867e-05
GP5 [NCBI] 8.27423e-06
MAFG [NCBI] 8.27423e-06
TUBB1 [NCBI] 7.92961e-06
ITGA2 [NCBI] 7.85834e-06
IL2 [NCBI] 7.78504e-06
TFPI [NCBI] 7.71543e-06
PIH [NCBI] 7.66965e-06
FCGR3A [NCBI] 7.41173e-06
MYH10 [NCBI] 7.3982e-06
NCKIPSD [NCBI] 7.3982e-06
RPS14 [NCBI] 7.3982e-06
F7 [NCBI] 7.31526e-06
PIGA [NCBI] 6.752e-06
IFRD1 [NCBI] 6.66803e-06
A1BG [NCBI] 6.5259e-06
CCNC [NCBI] 6.39482e-06
GP1BB [NCBI] 6.39482e-06
PRG4 [NCBI] 6.39482e-06
GP6 [NCBI] 5.85928e-06
DLAT [NCBI] 5.77e-06
CYCS [NCBI] 5.77e-06
HAX1 [NCBI] 5.60458e-06
TAP2 [NCBI] 5.55717e-06
SALL4 [NCBI] 5.4541e-06
CLCN7 [NCBI] 5.38367e-06
WIPF1 [NCBI] 5.38367e-06
DUSP2 [NCBI] 5.1285e-06
FUT8 [NCBI] 5.1285e-06
MS [NCBI] 5.00316e-06
CYP2C9 [NCBI] 4.88461e-06
VIPR1 [NCBI] 4.85661e-06
TAP1 [NCBI] 4.72141e-06
PMM2 [NCBI] 4.71274e-06
HOXA10 [NCBI] 4.71274e-06
CXCL12 [NCBI] 4.59964e-06
WASL [NCBI] 4.53871e-06
FES [NCBI] 4.53871e-06
PROM1 [NCBI] 4.52089e-06
ELAC2 [NCBI] 4.49797e-06
ANG [NCBI] 4.49797e-06
BACH1 [NCBI] 4.45822e-06
PRKCQ [NCBI] 4.41942e-06
PRKCA [NCBI] 4.41259e-06
ABCG5 [NCBI] 4.38153e-06
FCGR1A [NCBI] 4.30831e-06
ABCG8 [NCBI] 4.30831e-06
MYOM2 [NCBI] 4.07547e-06
FCGR2B [NCBI] 3.9852e-06
PLEK [NCBI] 3.95621e-06
CYP2C8 [NCBI] 3.84528e-06
DPYD [NCBI] 3.66815e-06
FAS [NCBI] 3.63677e-06
INPPL1 [NCBI] 3.59796e-06
MAP2K4 [NCBI] 3.48758e-06
DKC1 [NCBI] 3.40462e-06
VKORC1 [NCBI] 3.16235e-06
FGF4 [NCBI] 2.98389e-06
ACHE [NCBI] 2.80296e-06
GBA [NCBI] 2.74442e-06
BCHE [NCBI] 2.59635e-06
ADCYAP1 [NCBI] 2.53891e-06
FAH [NCBI] 2.45159e-06
SPN [NCBI] 2.28243e-06
CD52 [NCBI] 2.20067e-06
CHI3L1 [NCBI] 2.18315e-06
CFH [NCBI] 2.08262e-06
APAF1 [NCBI] 2.01961e-06
EDN1 [NCBI] 1.96687e-06
CCR3 [NCBI] 1.71953e-06
HBB [NCBI] 1.67783e-06
DDIT3 [NCBI] 1.66618e-06
CCL5 [NCBI] 1.62067e-06
FLT1 [NCBI] 1.56081e-06
MBL2 [NCBI] 1.54501e-06
ARID4A [NCBI] 1.45934e-06
CXCL1 [NCBI] 1.42586e-06
OSM [NCBI] 1.40255e-06
UGT1A1 [NCBI] 1.31397e-06
PGF [NCBI] 1.30129e-06
SDC1 [NCBI] 1.25605e-06
CNTF [NCBI] 1.23612e-06
PTGS2 [NCBI] 1.1625e-06
PTH [NCBI] 1.15608e-06
TERT [NCBI] 1.15275e-06
CAT [NCBI] 1.09212e-06
CDKN1B [NCBI] 1.0235e-06
TPO [NCBI] 1.01086e-06
FASLG [NCBI] 9.97605e-07
E2F1 [NCBI] 9.83048e-07
F8 [NCBI] 9.50173e-07
CYP3A4 [NCBI] 9.38512e-07
LPL [NCBI] 9.37528e-07
MTHFR [NCBI] 9.12195e-07
SLC2A1 [NCBI] 8.85145e-07
CCND1 [NCBI] 8.58336e-07
ENG [NCBI] 8.47847e-07
CDKN1A [NCBI] 8.05094e-07
DHFR [NCBI] 7.33827e-07
ABCB1 [NCBI] 7.13779e-07
F2 [NCBI] 6.89988e-07
BCR [NCBI] 6.66949e-07
FLT3 [NCBI] 6.58752e-07
GJB2 [NCBI] 4.70528e-07
F5 [NCBI] 4.69018e-07
TNF [NCBI] 4.06653e-07
CASP3 [NCBI] 3.16e-07
G6PD [NCBI] 2.14857e-07
CALCA [NCBI] 1.30384e-07
TRH [NCBI] 1.12379e-07
MPO [NCBI] 1.00335e-07
TGFB1 [NCBI] 9.54231e-08
AFP [NCBI] 8.5646e-08
HLA-DRB1 [NCBI] 7.65788e-08
VEGFA [NCBI] 6.49471e-08
HRAS [NCBI] 5.794e-08
HFE [NCBI] 2.42178e-08
PCNA [NCBI] 1.9937e-08
IL6 [NCBI] 1.78677e-08
AKT1 [NCBI] 1.14439e-08
HGF [NCBI] 7.74182e-09
CD68 [NCBI] 3.86508e-09
IL1RN [NCBI] 1.30283e-09




OMIM


OMIM Link Information
gain
01
thrombocytopenia-absent radius syndrome [NCBI] 0.021677
thrombocytopenic purpura, autoimmune [NCBI] 0.00398061
PF4 [NCBI] 0.00300268
thrombasthenia-thrombocytopenia, hereditary [NCBI] 0.00256974
WAS [NCBI] 0.00192542
GPS [NCBI] 0.00159882
THC2 [NCBI] 0.00134605
MHA [NCBI] 0.00129069
SLE [NCBI] 0.000990009
FTNS [NCBI] 0.000951474
MYH9 [NCBI] 0.000912361
SBS [NCBI] 0.000910426
hemangioma-thrombocytopenia syndrome [NCBI] 0.000882438
giant platelet syndrome [NCBI] 0.000775172
THC1 [NCBI] 0.000713962
CF [NCBI] 0.000580277
epstein syndrome [NCBI] 0.000557578
dianzani autoimmune lymphoproliferative disease [NCBI] 0.000553779
RA [NCBI] 0.000530114
GHDD [NCBI] 0.000501042
WAS [NCBI] 0.000493094
TTP [NCBI] 0.000474424
eosinophilia, familial [NCBI] 0.000462003
thrombocytopenia, autosomal recessive [NCBI] 0.000462003
THPO [NCBI] 0.000387602
MPL [NCBI] 0.000376272
visceral neuropathy, familial, autosomal recessive [NCBI] 0.000364525
dyserythropoietic anemia with thrombocytopenia [NCBI] 0.000330646
CAMT [NCBI] 0.000330646
klippel-trenaunay-weber syndrome [NCBI] 0.000308379
GATA1 [NCBI] 0.000252811
bernard-soulier syndrome, benign autosomal dominant [NCBI] 0.00024794
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis [NCBI] 0.00024794
ALPS [NCBI] 0.000211622
ITGA2 [NCBI] 0.000200618
platelet disorder, familial, with associated myeloid malignancy [NCBI] 0.000193589
TCPT [NCBI] 0.000193589
aHUS [NCBI] 0.000190248
platelet glycoprotein iv deficiency [NCBI] 0.000170844
radioulnar synostosis with amegakaryocytic thrombocytopenia [NCBI] 0.000165264
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 0.000131848
ITGB3 [NCBI] 0.000128033
MASTL [NCBI] 0.000127754
ivic syndrome [NCBI] 0.000120517
TPMT [NCBI] 0.000119512
ZFPM1 [NCBI] 0.000108788
ADAMTS13 [NCBI] 0.000106368
MG [NCBI] 0.00010283
EPO [NCBI] 0.000100221
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked [NCBI] 9.29327e-05
CD36 [NCBI] 9.13231e-05
RUNX1 [NCBI] 8.63635e-05
myeloproliferative disease, autosomal recessive [NCBI] 8.26171e-05
spastic paraplegia and evans syndrome [NCBI] 8.26171e-05
macrothrombocytopenia and progressive sensorineural deafness [NCBI] 8.26171e-05
CDG2F [NCBI] 8.26171e-05
osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension [NCBI] 8.26171e-05
stormorken syndrome [NCBI] 8.26171e-05
giant platelet syndrome with thrombocytopenia [NCBI] 8.26171e-05
IN [NCBI] 8.26171e-05
thrombocytopenia with elevated serum iga and renal disease [NCBI] 8.26171e-05
platelet disorder, undefined [NCBI] 8.26171e-05
von willebrand disease [NCBI] 8.19272e-05
antiphospholipid syndrome [NCBI] 7.86095e-05
FLI1 [NCBI] 7.60522e-05
HHS [NCBI] 7.33791e-05
GP1BA [NCBI] 6.55931e-05
CXCL12 [NCBI] 6.44715e-05
MYH10 [NCBI] 6.38558e-05
JBS [NCBI] 6.33094e-05
revesz syndrome [NCBI] 6.02438e-05
glanzmann thrombasthenia, autosomal dominant [NCBI] 6.02438e-05
thrombocytopenia, cyclic [NCBI] 6.02438e-05
IFRD1 [NCBI] 5.00912e-05
HOXA11 [NCBI] 5.00912e-05
HPA-2 [NCBI] 5.00912e-05
C1GALT1 [NCBI] 5.00912e-05
HTR2B [NCBI] 4.49059e-05
RPS14 [NCBI] 4.49059e-05
PECAM1 [NCBI] 4.49059e-05
thrombasthenia of glanzmann and naegeli [NCBI] 4.33414e-05
SDS [NCBI] 4.28941e-05
PD [NCBI] 4.17007e-05
RABGGTA [NCBI] 4.15441e-05
ATOX1 [NCBI] 4.15441e-05
NFE2 [NCBI] 4.15441e-05
DKC [NCBI] 4.03126e-05
mevalonic aciduria [NCBI] 3.92909e-05
CCNC [NCBI] 3.90485e-05
CEACAM5 [NCBI] 3.76125e-05
IFNA2 [NCBI] 3.7063e-05
TPH1 [NCBI] 3.7063e-05
congenital disorder of glycosylation, type i/iix [NCBI] 3.66758e-05
FHL2 [NCBI] 3.66758e-05
PTH [NCBI] 3.47329e-05
radioulnar synostosis [NCBI] 3.44515e-05
F3 [NCBI] 3.41554e-05
HTR2A [NCBI] 3.2776e-05
JAK2 [NCBI] 3.26244e-05
HPS2 [NCBI] 3.25193e-05
TNF [NCBI] 3.12663e-05
VEGF [NCBI] 3.01449e-05
sea-blue histiocyte disease [NCBI] 2.92894e-05
thiopurine s-methyltransferase deficiency [NCBI] 2.92894e-05
PTTG1 [NCBI] 2.90036e-05
AP3B1 [NCBI] 2.90036e-05
RP [NCBI] 2.85155e-05
von willebrand disease, recessive form [NCBI] 2.79131e-05
CD [NCBI] 2.78299e-05
IFNA1 [NCBI] 2.72263e-05
CXCR4 [NCBI] 2.6307e-05
TNFRSF1B [NCBI] 2.33198e-05
ACADS [NCBI] 2.29036e-05
KLK3 [NCBI] 2.28827e-05
pearson marrow-pancreas syndrome [NCBI] 2.25552e-05
PMM2 [NCBI] 2.25054e-05
TFPI [NCBI] 2.23602e-05
cirrhosis, familial [NCBI] 2.17005e-05
factor xii deficiency [NCBI] 2.17005e-05
immunoosseous dysplasia, schimke type [NCBI] 2.08989e-05
TRMA [NCBI] 2.08989e-05
DPYD [NCBI] 1.98251e-05
IPEX [NCBI] 1.94333e-05
TNFRSF6 [NCBI] 1.92636e-05
neuraminidase deficiency with beta-galactosidase deficiency [NCBI] 1.73193e-05
NS1 [NCBI] 1.65276e-05
CSF3 [NCBI] 1.62942e-05
FOXP3 [NCBI] 1.61032e-05
OPTB1 [NCBI] 1.53665e-05
LIPC [NCBI] 1.52084e-05
IL2 [NCBI] 1.3464e-05
tyrosinemia, type i [NCBI] 1.32555e-05
CDLS1 [NCBI] 1.26152e-05
CLL [NCBI] 1.20222e-05
RBS [NCBI] 1.13325e-05
APOE [NCBI] 1.02439e-05
KDR [NCBI] 9.2964e-06
BCHE [NCBI] 8.77063e-06
CDG1A [NCBI] 8.25646e-06
PCNA [NCBI] 7.70385e-06
TYMS [NCBI] 7.69061e-06
lymphoma, non-hodgkin, familial [NCBI] 6.99145e-06
OSM [NCBI] 5.83206e-06
HEMB [NCBI] 5.32568e-06
AFP [NCBI] 5.17861e-06
MPO [NCBI] 4.6286e-06
ACHE [NCBI] 1.74162e-06
CNTF [NCBI] 1.54752e-06
G6PD [NCBI] 1.40124e-06
SLOS [NCBI] 8.29485e-07
XDH [NCBI] 7.28663e-07
ACH [NCBI] 6.66301e-07
BBS [NCBI] 4.47663e-07
VHL [NCBI] 4.20553e-07
CHS [NCBI] 3.7826e-07
DHFR [NCBI] 2.03752e-07
CAT [NCBI] 4.54543e-08
HPS [NCBI] 2.75358e-08
PCD [NCBI] 1.33994e-08
LPL [NCBI] 7.32218e-09
HBB [NCBI] 3.26685e-10




Database Center for Life Science