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MeSH keywords -> Related genes, diseases (OMIM)


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01 Twins, Monozygotic [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000992385
AIS [NCBI] 0.000161588
BP36 [NCBI] 0.000138629
BP37 [NCBI] 0.000138629
MYAS1 [NCBI] 0.000138629
BP39 [NCBI] 0.000138629
BP38 [NCBI] 0.000138629
DFNA18 [NCBI] 0.000113359
WG [NCBI] 7.1761e-05
H19 [NCBI] 5.61317e-05
AIR [NCBI] 4.06651e-05
VUR [NCBI] 2.38348e-05
SLC6A4 [NCBI] 1.39452e-05
FMR1 [NCBI] 1.18814e-05
GER [NCBI] 1.07225e-05
SHBG [NCBI] 1.00751e-05
APOB [NCBI] 9.29354e-06
NOD2 [NCBI] 8.06338e-06
LEPR [NCBI] 8.04515e-06
CFTR [NCBI] 6.9714e-06
ADIPOQ [NCBI] 6.66563e-06
CYP2A6 [NCBI] 6.59944e-06
CHD7 [NCBI] 5.31581e-06
SRY [NCBI] 5.01295e-06
APOE [NCBI] 4.69848e-06
TROVE2 [NCBI] 4.68411e-06
LEP [NCBI] 4.56578e-06
ATP1A2 [NCBI] 4.238e-06
KAL1 [NCBI] 4.16468e-06
MLL [NCBI] 4.16129e-06
LPL [NCBI] 4.16064e-06
VHL [NCBI] 4.03586e-06
HLA-DQB1 [NCBI] 3.88334e-06
SH2D1A [NCBI] 3.75451e-06
CETP [NCBI] 3.73603e-06
COMT [NCBI] 3.69127e-06
PTPRN [NCBI] 3.66426e-06
PIGA [NCBI] 3.64429e-06
RETN [NCBI] 3.28991e-06
HTR2A [NCBI] 3.25088e-06
AXIN1 [NCBI] 3.19836e-06
ETV6 [NCBI] 3.08315e-06
LVRN [NCBI] 3.02212e-06
POU6F2 [NCBI] 2.89993e-06
AUTS2 [NCBI] 2.8493e-06
D2HGDH [NCBI] 2.80375e-06
SEPX1 [NCBI] 2.80375e-06
INS [NCBI] 2.61085e-06
AMT [NCBI] 2.59819e-06
RCN2 [NCBI] 2.57144e-06
PPIE [NCBI] 2.57144e-06
RARS [NCBI] 2.54618e-06
SLC6A3 [NCBI] 2.53419e-06
NAGLU [NCBI] 2.52225e-06
GLS [NCBI] 2.49953e-06
BTK [NCBI] 2.48615e-06
IGF1 [NCBI] 2.48083e-06
SLC17A5 [NCBI] 2.45723e-06
DRD4 [NCBI] 2.44445e-06
SLC27A4 [NCBI] 2.43747e-06
POU3F4 [NCBI] 2.43747e-06
VWF [NCBI] 2.3829e-06
ABHD5 [NCBI] 2.38289e-06
TSNAX [NCBI] 2.38289e-06
GRK4 [NCBI] 2.38289e-06
ZIC2 [NCBI] 2.36607e-06
ACADVL [NCBI] 2.36607e-06
TAS2R38 [NCBI] 2.34985e-06
SACS [NCBI] 2.31905e-06
KCNMB1 [NCBI] 2.29022e-06
GYS1 [NCBI] 2.29022e-06
HTT [NCBI] 2.28784e-06
TBX5 [NCBI] 2.27646e-06
RDH5 [NCBI] 2.26311e-06
ANKK1 [NCBI] 2.21332e-06
ATN1 [NCBI] 2.16848e-06
HSD3B1 [NCBI] 2.15793e-06
GPR143 [NCBI] 2.13754e-06
EPHX2 [NCBI] 2.12768e-06
GAD1 [NCBI] 2.12768e-06
DCX [NCBI] 2.12768e-06
FABP4 [NCBI] 2.09027e-06
CNBP [NCBI] 2.08138e-06
GAD2 [NCBI] 2.07266e-06
FLCN [NCBI] 2.03938e-06
GEM [NCBI] 2.00839e-06
CYP27B1 [NCBI] 2.00096e-06
RAD23B [NCBI] 1.99366e-06
MFGE8 [NCBI] 1.98647e-06
APTX [NCBI] 1.97939e-06
CHRM2 [NCBI] 1.97242e-06
SPINK5 [NCBI] 1.93912e-06
PRTN3 [NCBI] 1.92646e-06
IRF6 [NCBI] 1.92026e-06
FLG [NCBI] 1.92026e-06
SFTPB [NCBI] 1.89628e-06
ABCG8 [NCBI] 1.89628e-06
GLA [NCBI] 1.89048e-06
ABCG5 [NCBI] 1.88475e-06
PRSS2 [NCBI] 1.868e-06
SCN1A [NCBI] 1.86255e-06
COL7A1 [NCBI] 1.85184e-06
MASP2 [NCBI] 1.82615e-06
CD177 [NCBI] 1.81627e-06
PPOX [NCBI] 1.81627e-06
CAPN10 [NCBI] 1.8066e-06
ADIPOR2 [NCBI] 1.80185e-06
FOXC2 [NCBI] 1.80185e-06
HRG [NCBI] 1.79714e-06
PTH [NCBI] 1.79632e-06
CYP2B6 [NCBI] 1.78787e-06
NCAM1 [NCBI] 1.78331e-06
HPRT1 [NCBI] 1.76551e-06
COL4A5 [NCBI] 1.75687e-06
IKZF1 [NCBI] 1.73597e-06
VDR [NCBI] 1.71682e-06
ADIPOR1 [NCBI] 1.68216e-06
DISC1 [NCBI] 1.66441e-06
NAIP [NCBI] 1.6507e-06
ATF4 [NCBI] 1.644e-06
ADH1C [NCBI] 1.6374e-06
HSD11B2 [NCBI] 1.63414e-06
CYR61 [NCBI] 1.60885e-06
REN [NCBI] 1.60885e-06
DDC [NCBI] 1.60275e-06
SOX2 [NCBI] 1.565e-06
ADRB1 [NCBI] 1.55947e-06
TGM1 [NCBI] 1.54327e-06
MC1R [NCBI] 1.52509e-06
XRCC3 [NCBI] 1.51752e-06
ADH1B [NCBI] 1.50763e-06
ACTB [NCBI] 1.50763e-06
FGB [NCBI] 1.49795e-06
TSC2 [NCBI] 1.48848e-06
COMP [NCBI] 1.48151e-06
ITGA2 [NCBI] 1.47238e-06
LRRK2 [NCBI] 1.4525e-06
MBP [NCBI] 1.44452e-06
SNAP25 [NCBI] 1.43349e-06
CDKN1C [NCBI] 1.40934e-06
IGFBP1 [NCBI] 1.39966e-06
COL2A1 [NCBI] 1.39207e-06
ATXN3 [NCBI] 1.39207e-06
APRT [NCBI] 1.37544e-06
XPC [NCBI] 1.36825e-06
CACNA1A [NCBI] 1.36825e-06
MYCN [NCBI] 1.35249e-06
ATXN1 [NCBI] 1.35078e-06
CYP1B1 [NCBI] 1.34736e-06
ABCA1 [NCBI] 1.34229e-06
STK11 [NCBI] 1.34062e-06
XPA [NCBI] 1.31462e-06
PIK3R1 [NCBI] 1.2827e-06
SMN1 [NCBI] 1.26971e-06
SDC1 [NCBI] 1.25434e-06
IGFBP3 [NCBI] 1.24752e-06
SOX9 [NCBI] 1.22385e-06
MATN1 [NCBI] 1.22258e-06
MBL2 [NCBI] 1.22003e-06
DBH [NCBI] 1.21374e-06
ADAMTS13 [NCBI] 1.2063e-06
AR [NCBI] 1.20326e-06
SGK1 [NCBI] 1.19419e-06
EPO [NCBI] 1.19294e-06
ADM [NCBI] 1.18708e-06
IGF2 [NCBI] 1.15757e-06
NR3C1 [NCBI] 1.1532e-06
F8 [NCBI] 1.14781e-06
DRD2 [NCBI] 1.14674e-06
ACHE [NCBI] 1.13492e-06
ERG [NCBI] 1.12996e-06
WAS [NCBI] 1.1158e-06
MEN1 [NCBI] 1.11085e-06
FABP7 [NCBI] 1.07959e-06
ERCC2 [NCBI] 1.07685e-06
JAG1 [NCBI] 1.06966e-06
MB [NCBI] 1.06699e-06
KCNH6 [NCBI] 1.06699e-06
MECP2 [NCBI] 1.06699e-06
HNF1B [NCBI] 1.05389e-06
PSEN2 [NCBI] 1.03705e-06
FHIT [NCBI] 1.01064e-06
SHH [NCBI] 1.00832e-06
ERBB2 [NCBI] 9.93926e-07
FLT3 [NCBI] 9.75708e-07
UCP3 [NCBI] 9.61689e-07
RUNX1 [NCBI] 9.40856e-07
TTR [NCBI] 9.00329e-07
EGR1 [NCBI] 8.97371e-07
PPARG [NCBI] 8.78375e-07
CD68 [NCBI] 8.26717e-07
PRL [NCBI] 8.22163e-07
PAX6 [NCBI] 7.80985e-07
ACP5 [NCBI] 7.67132e-07
GSTP1 [NCBI] 7.38047e-07
CTSL1 [NCBI] 7.26386e-07
ESR1 [NCBI] 7.16557e-07
MTHFR [NCBI] 6.02504e-07
IL6 [NCBI] 5.79359e-07
JAK2 [NCBI] 5.77048e-07
AFP [NCBI] 5.02845e-07
STAT3 [NCBI] 4.71142e-07
VEGFA [NCBI] 3.77397e-07
AVP [NCBI] 3.4027e-07
TH [NCBI] 3.36389e-07
NPY [NCBI] 2.45952e-07
TNF [NCBI] 1.07439e-08



OMIM


 OMIM Link Information
gain		 01
chiari malformation type i [NCBI] 0.00157791
constricting bands, congenital [NCBI] 0.00150788
HFM [NCBI] 0.00119466
autism [NCBI] 0.0011208
cayler cardiofacial syndrome [NCBI] 0.00110482
MENOQ1 [NCBI] 0.000934592
ANON1 [NCBI] 0.000877227
mammographic density [NCBI] 0.000861524
3-@hydroxyisobutyric aciduria [NCBI] 0.000861524
theophylline biotransformation [NCBI] 0.000861524
amobarbital, deficient n-hydroxylation of [NCBI] 0.000861524
varadi-papp syndrome [NCBI] 0.000784736
twinning, dizygotic [NCBI] 0.000625691
hypertelorism, microtia, facial clefting syndrome [NCBI] 0.000598424
bone size quantitative trait locus 1 [NCBI] 0.000500438
cerebellar atrophy with progressive microcephaly [NCBI] 0.000500438
tune deafness [NCBI] 0.000500438
astigmatism [NCBI] 0.000500438
BWS [NCBI] 0.000467137
twinning, monozygotic [NCBI] 0.000450879
fibrochondrogenesis [NCBI] 0.000437549
DYX6 [NCBI] 0.000437549
coronary heart disease, susceptibility to, 2 [NCBI] 0.000391328
holoprosencephaly [NCBI] 0.0003896
corpus callosum, agenesis of, with facial anomalies and robin sequence [NCBI] 0.000354925
immunoglobulin m, level of [NCBI] 0.000354925
kabuki syndrome [NCBI] 0.00034689
MAFD2 [NCBI] 0.000327888
achalasia, familial esophageal [NCBI] 0.000325009
IH [NCBI] 0.000325009
cluster headache, familial [NCBI] 0.000325009
MNG1 [NCBI] 0.000325009
urogenital adysplasia, hereditary [NCBI] 0.000318896
DMD [NCBI] 0.000317225
RA [NCBI] 0.000302594
gastroesophageal reflux [NCBI] 0.000299704
CF [NCBI] 0.00029276
wernicke-korsakoff syndrome [NCBI] 0.000277847
FSHMD1A [NCBI] 0.000264896
centralopathic epilepsy [NCBI] 0.000258666
BULN1 [NCBI] 0.000258666
WM1 [NCBI] 0.000258666
ETL2 [NCBI] 0.000226328
mast cell disease [NCBI] 0.00021503
dystonia, juvenile-onset [NCBI] 0.000213663
neuronal intranuclear inclusion disease [NCBI] 0.000213663
OFC1 [NCBI] 0.000203158
AIC [NCBI] 0.000188322
PAND1 [NCBI] 0.000188322
alopecia areata 1 [NCBI] 0.000188322
MS [NCBI] 0.000184095
RSTS [NCBI] 0.000168517
caudal duplication anomaly [NCBI] 0.000158309
SRS [NCBI] 0.000154033
aromatic l-amino acid decarboxylase deficiency [NCBI] 0.000146536
JBTS1 [NCBI] 0.000142237
LIP [NCBI] 0.000141445
SCDO1 [NCBI] 0.000141445
EHBA [NCBI] 0.000137536
oeis complex [NCBI] 0.000137536
DYX1 [NCBI] 0.000136513
TD1 [NCBI] 0.000135997
dubowitz syndrome [NCBI] 0.0001278
CPI [NCBI] 0.000124579
IDD [NCBI] 0.000124115
breast cancer [NCBI] 0.000123562
vitamin d-dependent rickets, type ii [NCBI] 0.000116887
GBD1 [NCBI] 0.000114184
myeloma, multiple [NCBI] 0.000110043
osteochondrosis deformans tibiae, familial infantile type [NCBI] 0.000106803
folate level in erythrocytes [NCBI] 0.000106803
colonic atresia [NCBI] 0.000106803
dysphasia, familial developmental [NCBI] 0.000106803
bile duct cysts [NCBI] 0.000106803
lip prints [NCBI] 0.000106803
subependymoma [NCBI] 0.000106803
facial dysmorphism, selective tooth agenesis, and choroid calcification [NCBI] 0.000106803
myoclonus, cerebellar ataxia, and deafness [NCBI] 0.000106803
PPAB [NCBI] 0.000106803
synovitis, granulomatous, with uveitis and cranial neuropathies [NCBI] 0.000102911
FRNS [NCBI] 9.84139e-05
HMS1 [NCBI] 9.69151e-05
bare lymphocyte syndrome, type ii [NCBI] 9.23412e-05
HD [NCBI] 8.88909e-05
SLE [NCBI] 8.46014e-05
DWS [NCBI] 8.42705e-05
ETM1 [NCBI] 8.31868e-05
lithium transport [NCBI] 7.91262e-05
acne, adult [NCBI] 7.91262e-05
arachnoid cysts, intracranial [NCBI] 7.91262e-05
colchicine resistance [NCBI] 7.91262e-05
periodontitis, chronic [NCBI] 7.91262e-05
craniosynostosis with ectopia lentis [NCBI] 7.91262e-05
langerhans cell histiocytosis [NCBI] 7.91262e-05
osteoporosis [NCBI] 7.7873e-05
lung cancer [NCBI] 7.47236e-05
RTT [NCBI] 6.96127e-05
NRCLP1 [NCBI] 6.9161e-05
tracheobronchial stenosis, congenital [NCBI] 6.87401e-05
HSAN5 [NCBI] 6.87401e-05
ovarian teratoma [NCBI] 6.87401e-05
say syndrome [NCBI] 6.87401e-05
coloboma of optic nerve [NCBI] 6.87401e-05
bile acid synthesis defect, congenital, 2 [NCBI] 6.87401e-05
androstenone, ability to smell [NCBI] 6.87401e-05
rokitansky-kuster-hauser syndrome [NCBI] 6.87401e-05
sodium-potassium-atpase activity of red cell [NCBI] 6.87401e-05
barraquer-simons syndrome [NCBI] 6.87401e-05
keratitis, hereditary [NCBI] 6.87401e-05
aprosencephaly syndrome [NCBI] 6.87401e-05
pena-shokeir syndrome, type i [NCBI] 6.84477e-05
AXIN1 [NCBI] 6.52743e-05
CDLS1 [NCBI] 6.37515e-05
EEG [NCBI] 6.20294e-05
hair whorl [NCBI] 6.20294e-05
brachydactyly-ectrodactyly with fibular aplasia or hypoplasia [NCBI] 6.20294e-05
tongue curling, folding, or rolling [NCBI] 6.20294e-05
goodpasture syndrome [NCBI] 6.20294e-05
oncocytoma [NCBI] 6.20294e-05
femur-fibula-ulna syndrome [NCBI] 6.20294e-05
atrioventricular conduction time [NCBI] 6.20294e-05
respiratory underresponsiveness to hypoxia and hypercapnia [NCBI] 6.20294e-05
hand clasping pattern [NCBI] 6.20294e-05
FMR1 [NCBI] 6.1923e-05
PPR [NCBI] 6.16078e-05
CDG1A [NCBI] 6.11721e-05
EPHX2 [NCBI] 6.04278e-05
PCOS1 [NCBI] 5.84205e-05
SMEI [NCBI] 5.82546e-05
lichen planus, familial [NCBI] 5.70643e-05
respiratory distress syndrome in premature infants [NCBI] 5.70643e-05
TINU [NCBI] 5.70643e-05
ACTB [NCBI] 5.4352e-05
sotos syndrome [NCBI] 5.39043e-05
OCA1B [NCBI] 5.31273e-05
nonarteritic anterior ischemic optic neuropathy, susceptibility to [NCBI] 5.31273e-05
gastroschisis [NCBI] 5.31273e-05
creatine phosphokinase, elevated serum [NCBI] 5.31273e-05
HPE4 [NCBI] 5.31273e-05
hypertelorism with esophageal abnormality and hypospadias [NCBI] 5.24704e-05
GTS [NCBI] 5.06687e-05
TD2 [NCBI] 4.98696e-05
pneumothorax, primary spontaneous [NCBI] 4.98696e-05
FHL2 [NCBI] 4.98696e-05
HSR [NCBI] 4.87813e-05
IS1 [NCBI] 4.83506e-05
VWS [NCBI] 4.73178e-05
OPLL [NCBI] 4.70948e-05
takayasu arteritis [NCBI] 4.70948e-05
klippel-trenaunay-weber syndrome [NCBI] 4.70385e-05
EIG [NCBI] 4.54595e-05
RHN [NCBI] 4.4681e-05
tobacco addiction, susceptibility to [NCBI] 4.4681e-05
macular dystrophy, vitelliform, adult-onset [NCBI] 4.4681e-05
SHBG [NCBI] 4.34996e-05
NETH [NCBI] 4.25474e-05
WZS [NCBI] 4.25474e-05
aryl hydrocarbon hydroxylase inducibility [NCBI] 4.25474e-05
hematopoietic stem cell kinetics, control of [NCBI] 4.25474e-05
SVAS [NCBI] 4.24591e-05
CYP1A1 [NCBI] 4.24492e-05
HPE2 [NCBI] 3.89108e-05
SHEP1 [NCBI] 3.73364e-05
BMND1 [NCBI] 3.73364e-05
OPPG [NCBI] 3.73364e-05
heart block, congenital [NCBI] 3.73364e-05
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 3.73364e-05
parkinson disease, mitochondrial [NCBI] 3.73364e-05
PI [NCBI] 3.66738e-05
PPS [NCBI] 3.58908e-05
SCZD9 [NCBI] 3.58908e-05
BHD [NCBI] 3.58908e-05
ADLTE [NCBI] 3.45556e-05
aging [NCBI] 3.45556e-05
CFTD [NCBI] 3.45556e-05
lymphedema-distichiasis syndrome [NCBI] 3.45556e-05
HPE3 [NCBI] 3.45556e-05
AD [NCBI] 3.41215e-05
kiaa0442 [NCBI] 3.37088e-05
ST3GAL6 [NCBI] 3.37088e-05
PFM [NCBI] 3.33161e-05
CSID [NCBI] 3.33161e-05
helicobacter pylori infection, susceptibility to [NCBI] 3.33161e-05
VDR [NCBI] 3.32967e-05
mucopolysaccharidosis type ii [NCBI] 3.29945e-05
thrombocytopenic purpura, autoimmune [NCBI] 3.29729e-05
infantile spasm syndrome, x-linked [NCBI] 3.21602e-05
longevity [NCBI] 3.21602e-05
thyroid hormonogenesis, genetic defect in, 2a [NCBI] 3.21602e-05
RSMD1 [NCBI] 3.21602e-05
LEPR [NCBI] 3.21431e-05
MAS [NCBI] 3.18664e-05
TSNAX [NCBI] 3.16902e-05
ACTG2 [NCBI] 3.16902e-05
BGS [NCBI] 3.10781e-05
OFD1 [NCBI] 3.10781e-05
APOB [NCBI] 3.04794e-05
GLS [NCBI] 3.019e-05
BFLS [NCBI] 3.00615e-05
stroke, ischemic [NCBI] 2.91037e-05
mucopolysaccharidosis type iiib [NCBI] 2.91037e-05
autonomic control, congenital failure of [NCBI] 2.91037e-05
polycythemia vera [NCBI] 2.91037e-05
ACE [NCBI] 2.85612e-05
krabbe disease [NCBI] 2.83283e-05
EDMD2 [NCBI] 2.81986e-05
aortic aneurysm, abdominal [NCBI] 2.73413e-05
pulmonary fibrosis, idiopathic [NCBI] 2.73413e-05
fraser syndrome [NCBI] 2.73413e-05
ADHD [NCBI] 2.70461e-05
VHL [NCBI] 2.67362e-05
CHNG2 [NCBI] 2.65274e-05
hodgkin lymphoma [NCBI] 2.65274e-05
sudden infant death syndrome [NCBI] 2.65274e-05
ALD [NCBI] 2.58579e-05
AMT [NCBI] 2.57502e-05
CFD [NCBI] 2.51573e-05
GYS1 [NCBI] 2.51573e-05
MG [NCBI] 2.51338e-05
MRXHF1 [NCBI] 2.50152e-05
charge syndrome [NCBI] 2.50152e-05
ZNF9 [NCBI] 2.46188e-05
RFX5 [NCBI] 2.46188e-05
osteoarthritis [NCBI] 2.43107e-05
LCA1 [NCBI] 2.43107e-05
SULT1A1 [NCBI] 2.41255e-05
SFTPD [NCBI] 2.41255e-05
RNR1 [NCBI] 2.32481e-05
SPDA1 [NCBI] 2.29919e-05
HSAS [NCBI] 2.29919e-05
NAGLU [NCBI] 2.28542e-05
IRF6 [NCBI] 2.24852e-05
CYP1A2 [NCBI] 2.24852e-05
mycobacterium tuberculosis, susceptibility to [NCBI] 2.23734e-05
testicular tumors [NCBI] 2.23734e-05
KCNQ1OT1 [NCBI] 2.21381e-05
FGB [NCBI] 2.21381e-05
RBS [NCBI] 2.12086e-05
SGBS1 [NCBI] 2.06593e-05
SCN1A [NCBI] 1.96963e-05
CMD1A [NCBI] 1.96201e-05
ALDH1A1 [NCBI] 1.9479e-05
PCTT [NCBI] 1.91279e-05
SJS1 [NCBI] 1.91279e-05
campomelic dysplasia [NCBI] 1.91279e-05
ETV6 [NCBI] 1.88721e-05
DISC1 [NCBI] 1.88721e-05
GCDH [NCBI] 1.86831e-05
GCPS [NCBI] 1.86525e-05
kartagener syndrome [NCBI] 1.86525e-05
malaria, susceptibility to [NCBI] 1.86525e-05
CETP [NCBI] 1.85002e-05
fructose intolerance, hereditary [NCBI] 1.85002e-05
COH1 [NCBI] 1.8193e-05
CBD [NCBI] 1.7984e-05
PIGA [NCBI] 1.78218e-05
ALDH2 [NCBI] 1.75105e-05
JAG1 [NCBI] 1.7361e-05
EDN1 [NCBI] 1.70732e-05
POAG [NCBI] 1.69018e-05
HLA-DRA [NCBI] 1.67992e-05
ADIPOQ [NCBI] 1.66671e-05
LPA [NCBI] 1.66671e-05
IGER [NCBI] 1.64979e-05
KAL1 [NCBI] 1.64116e-05
COL7A1 [NCBI] 1.60487e-05
LI1 [NCBI] 1.57264e-05
DM2 [NCBI] 1.53576e-05
F2 [NCBI] 1.50822e-05
REN [NCBI] 1.50822e-05
ALGS1 [NCBI] 1.49993e-05
MTND4 [NCBI] 1.47009e-05
FA [NCBI] 1.46615e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 1.46095e-05
BIRC1 [NCBI] 1.4344e-05
CSA [NCBI] 1.43127e-05
TGFB1 [NCBI] 1.42582e-05
IL10 [NCBI] 1.38483e-05
TSC2 [NCBI] 1.37699e-05
obesity [NCBI] 1.36632e-05
HNPP [NCBI] 1.36632e-05
TNF [NCBI] 1.34957e-05
VEGF [NCBI] 1.33898e-05
OCP [NCBI] 1.33515e-05
WBS [NCBI] 1.31106e-05
HRG [NCBI] 1.311e-05
BTK [NCBI] 1.25214e-05
ED1 [NCBI] 1.2464e-05
GH1 [NCBI] 1.18795e-05
ARMD1 [NCBI] 1.13813e-05
COMT [NCBI] 1.09563e-05
IGFALS [NCBI] 1.05279e-05
DDC [NCBI] 1.01983e-05
FTD [NCBI] 9.74549e-06
LEP [NCBI] 9.38816e-06
CMT1A [NCBI] 9.2942e-06
hemophilia a [NCBI] 8.96438e-06
FMF [NCBI] 8.6993e-06
IDDM [NCBI] 8.57481e-06
COMP [NCBI] 7.87683e-06
APRT [NCBI] 6.99313e-06
MDD [NCBI] 5.89577e-06
MBL2 [NCBI] 5.54928e-06
APOE [NCBI] 5.54404e-06
panencephalitis, subacute sclerosing [NCBI] 5.21466e-06
WT1 [NCBI] 5.12297e-06
SCA1 [NCBI] 4.76817e-06
PD [NCBI] 4.20418e-06
MB [NCBI] 4.14175e-06
SCZD [NCBI] 4.118e-06
TS [NCBI] 4.08471e-06
hypercholesterolemia, autosomal dominant [NCBI] 3.82028e-06
ACP5 [NCBI] 2.89288e-06
KSS [NCBI] 2.71343e-06
NPY [NCBI] 2.4793e-06
PCD [NCBI] 2.3576e-06
LPL [NCBI] 2.15239e-06
TTR [NCBI] 1.96684e-06
PMD [NCBI] 1.63732e-06
MBP [NCBI] 1.60857e-06
TH [NCBI] 1.23462e-06
AVP [NCBI] 1.20738e-06
DRPLA [NCBI] 9.62661e-07
AIS [NCBI] 9.25457e-07
AR [NCBI] 8.76667e-07
WAS [NCBI] 7.77428e-07
fragile x mental retardation syndrome [NCBI] 6.00911e-07
PJS [NCBI] 5.45801e-07
CEACAM5 [NCBI] 5.24929e-07
PTH [NCBI] 4.5719e-07
CD [NCBI] 3.9674e-07
PRL [NCBI] 3.65669e-07
EPO [NCBI] 2.99155e-07
DGS [NCBI] 2.77259e-07
leber optic atrophy [NCBI] 1.94525e-07
AFP [NCBI] 7.37228e-08
ACHE [NCBI] 4.92841e-08
GIST [NCBI] 3.16146e-08
NPPA [NCBI] 2.97787e-08
MODY [NCBI] 2.14937e-08
dystrophia myotonica 1 [NCBI] 1.7331e-08
CFTR [NCBI] 6.28875e-10



Database Center for Life Science