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MeSH keywords -> Related genes, diseases (OMIM)


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01 Diseases in Twins [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000821332
SLI1 [NCBI] 0.000283087
BP24 [NCBI] 0.000283087
DYX6 [NCBI] 0.000283087
SLI2 [NCBI] 0.000283087
AREI [NCBI] 0.000283087
DFNA18 [NCBI] 0.000222409
ANE1 [NCBI] 0.000222409
WFS2 [NCBI] 0.000222409
DYX9 [NCBI] 0.000222409
HSCRM1 [NCBI] 0.000199549
H19 [NCBI] 9.74364e-05
HFM [NCBI] 7.78245e-05
FOP [NCBI] 5.92534e-05
SLC6A4 [NCBI] 5.67007e-05
GTS [NCBI] 4.79706e-05
VUR [NCBI] 3.69403e-05
MLL [NCBI] 3.08835e-05
TROVE2 [NCBI] 2.68701e-05
SLC6A3 [NCBI] 2.56143e-05
CFTR [NCBI] 2.46732e-05
AIS [NCBI] 2.04699e-05
DISC1 [NCBI] 2.00189e-05
APOE [NCBI] 1.8117e-05
FMR1 [NCBI] 1.74134e-05
MAOA [NCBI] 1.72204e-05
LVRN [NCBI] 1.38399e-05
AGA [NCBI] 1.38185e-05
ACHE [NCBI] 1.37416e-05
NOD2 [NCBI] 1.35034e-05
DHCR7 [NCBI] 1.34349e-05
MAOB [NCBI] 1.30254e-05
HLA-DQB1 [NCBI] 1.2896e-05
COL7A1 [NCBI] 1.17999e-05
ELTD1 [NCBI] 1.146e-05
CLCA4 [NCBI] 1.146e-05
MPZ [NCBI] 1.04278e-05
PCDHA4 [NCBI] 9.97906e-06
SHC2 [NCBI] 9.97906e-06
FGFRL1 [NCBI] 9.97906e-06
SH2D1A [NCBI] 9.95961e-06
HTR2A [NCBI] 9.66507e-06
COMT [NCBI] 9.64219e-06
POU6F2 [NCBI] 9.54572e-06
PPIE [NCBI] 9.54572e-06
COL2A1 [NCBI] 9.37326e-06
PIGA [NCBI] 9.20582e-06
GNB1L [NCBI] 9.2005e-06
APOB [NCBI] 9.03354e-06
AFP [NCBI] 8.9938e-06
PTPRN [NCBI] 8.67958e-06
ACCN2 [NCBI] 8.6679e-06
TSNAX [NCBI] 8.6679e-06
AMN [NCBI] 8.6679e-06
SRY [NCBI] 8.62795e-06
TNFAIP1 [NCBI] 8.45323e-06
PLXNA2 [NCBI] 8.26258e-06
SOX11 [NCBI] 8.26258e-06
CETP [NCBI] 7.94461e-06
AMT [NCBI] 7.93534e-06
VPS33B [NCBI] 7.93534e-06
DHCR24 [NCBI] 7.66094e-06
SEPT5 [NCBI] 7.66094e-06
C2 [NCBI] 7.4247e-06
OFD1 [NCBI] 7.31785e-06
GK [NCBI] 7.31785e-06
MATN1 [NCBI] 7.30492e-06
ETV6 [NCBI] 7.27131e-06
ACADVL [NCBI] 7.21732e-06
SLC17A5 [NCBI] 7.03254e-06
POU3F4 [NCBI] 7.03254e-06
KIAA0319 [NCBI] 7.03254e-06
ABHD5 [NCBI] 6.94718e-06
CFB [NCBI] 6.94718e-06
ND5 [NCBI] 6.86592e-06
CCHCR1 [NCBI] 6.86592e-06
RDH5 [NCBI] 6.86592e-06
APOC2 [NCBI] 6.78839e-06
BBS2 [NCBI] 6.78839e-06
DCX [NCBI] 6.71424e-06
PTPRJ [NCBI] 6.71424e-06
CHD7 [NCBI] 6.64322e-06
GABRA2 [NCBI] 6.64322e-06
TAZ [NCBI] 6.57505e-06
GEM [NCBI] 6.57505e-06
TBX5 [NCBI] 6.50953e-06
HMGCR [NCBI] 6.44646e-06
LAMB1 [NCBI] 6.44646e-06
RHCE [NCBI] 6.38566e-06
EFNB1 [NCBI] 6.38566e-06
WAS [NCBI] 6.35271e-06
ATN1 [NCBI] 6.32698e-06
NODAL [NCBI] 6.27027e-06
BBS1 [NCBI] 6.27027e-06
WHSC1 [NCBI] 6.21541e-06
KL [NCBI] 6.21541e-06
MFGE8 [NCBI] 6.21541e-06
PYGM [NCBI] 6.11078e-06
CENPC1 [NCBI] 6.11078e-06
CNBP [NCBI] 6.06081e-06
GABRB3 [NCBI] 6.06081e-06
CLCA1 [NCBI] 6.06081e-06
ERCC8 [NCBI] 6.01228e-06
CDSN [NCBI] 6.01228e-06
RECQL4 [NCBI] 5.8311e-06
CYP27B1 [NCBI] 5.8311e-06
IL6 [NCBI] 5.81752e-06
ARMS2 [NCBI] 5.78871e-06
SFTPB [NCBI] 5.74736e-06
HTR1A [NCBI] 5.70702e-06
BSCL2 [NCBI] 5.70702e-06
DDC [NCBI] 5.66762e-06
DAOA [NCBI] 5.66762e-06
TGFB3 [NCBI] 5.55472e-06
FGG [NCBI] 5.44898e-06
TBX1 [NCBI] 5.44898e-06
GLB1 [NCBI] 5.44898e-06
CD79B [NCBI] 5.38205e-06
IKZF1 [NCBI] 5.34957e-06
NCAM1 [NCBI] 5.31771e-06
FLCN [NCBI] 5.28645e-06
HBG2 [NCBI] 5.28645e-06
APOA4 [NCBI] 5.25577e-06
SLC18A2 [NCBI] 5.22564e-06
CENPB [NCBI] 5.19606e-06
NAGA [NCBI] 5.19606e-06
SPINK5 [NCBI] 5.19606e-06
TPH1 [NCBI] 5.19606e-06
FOXP2 [NCBI] 5.16699e-06
IL12RB1 [NCBI] 5.13843e-06
S100B [NCBI] 5.11035e-06
HAPLN1 [NCBI] 5.08274e-06
ATRX [NCBI] 5.05558e-06
CNR1 [NCBI] 5.02887e-06
LRP1 [NCBI] 5.00258e-06
IRS1 [NCBI] 5.00224e-06
SNAP25 [NCBI] 4.9767e-06
SOX2 [NCBI] 4.92613e-06
DTNBP1 [NCBI] 4.92613e-06
FOXC2 [NCBI] 4.90142e-06
IRF6 [NCBI] 4.90142e-06
HBD [NCBI] 4.85309e-06
C3 [NCBI] 4.85309e-06
NDP [NCBI] 4.85309e-06
KRT10 [NCBI] 4.82944e-06
GJB2 [NCBI] 4.75302e-06
SCN1A [NCBI] 4.73813e-06
A2M [NCBI] 4.71608e-06
IL23R [NCBI] 4.65165e-06
BEST1 [NCBI] 4.58967e-06
IL18R1 [NCBI] 4.58967e-06
SLC4A1 [NCBI] 4.56952e-06
CD177 [NCBI] 4.52996e-06
SLC12A3 [NCBI] 4.52996e-06
PPOX [NCBI] 4.51053e-06
VHL [NCBI] 4.4895e-06
MC1R [NCBI] 4.43507e-06
OPA1 [NCBI] 4.32809e-06
HSD11B2 [NCBI] 4.27715e-06
COL11A2 [NCBI] 4.27715e-06
GAA [NCBI] 4.26052e-06
KAL1 [NCBI] 4.26052e-06
ADH1C [NCBI] 4.22776e-06
SLC22A5 [NCBI] 4.21163e-06
CYR61 [NCBI] 4.19566e-06
TGM1 [NCBI] 4.16419e-06
ERCC6 [NCBI] 4.13333e-06
TSHR [NCBI] 4.07333e-06
ESD [NCBI] 4.07333e-06
LIPC [NCBI] 4.07333e-06
RPGR [NCBI] 4.04415e-06
ITGA2 [NCBI] 4.00136e-06
FGFR1 [NCBI] 3.98735e-06
NAIP [NCBI] 3.97347e-06
APRT [NCBI] 3.97347e-06
SHOX [NCBI] 3.90579e-06
NRG1 [NCBI] 3.86653e-06
RELN [NCBI] 3.85365e-06
G6PD [NCBI] 3.8496e-06
HBA1 [NCBI] 3.82822e-06
APOC3 [NCBI] 3.82822e-06
FGB [NCBI] 3.80318e-06
LCAT [NCBI] 3.77854e-06
TYRP1 [NCBI] 3.75428e-06
ADH1B [NCBI] 3.74228e-06
APOA5 [NCBI] 3.70685e-06
MLX [NCBI] 3.70685e-06
NPPB [NCBI] 3.69521e-06
CD1D [NCBI] 3.69521e-06
TSC2 [NCBI] 3.68366e-06
DBH [NCBI] 3.68366e-06
FAH [NCBI] 3.63829e-06
CYP27A1 [NCBI] 3.60511e-06
NLRP3 [NCBI] 3.60511e-06
ABCA1 [NCBI] 3.58337e-06
MTRR [NCBI] 3.56193e-06
MTR [NCBI] 3.5096e-06
ADRB3 [NCBI] 3.44905e-06
CASR [NCBI] 3.41964e-06
LEPR [NCBI] 3.40034e-06
CDKN1C [NCBI] 3.28938e-06
CFH [NCBI] 3.24543e-06
ATXN1 [NCBI] 3.22819e-06
IRS2 [NCBI] 3.16937e-06
JAG1 [NCBI] 3.16937e-06
APOA1 [NCBI] 3.15298e-06
COMP [NCBI] 3.15298e-06
LRRK2 [NCBI] 3.12872e-06
ATXN3 [NCBI] 3.12072e-06
EDN1 [NCBI] 3.12072e-06
SHC1 [NCBI] 3.10484e-06
GATA1 [NCBI] 3.0354e-06
STK11 [NCBI] 3.0204e-06
COL1A1 [NCBI] 2.94757e-06
BDNF [NCBI] 2.93493e-06
DRD4 [NCBI] 2.89864e-06
ZAP70 [NCBI] 2.86466e-06
SCN5A [NCBI] 2.81187e-06
MYCN [NCBI] 2.78617e-06
LPL [NCBI] 2.71365e-06
KCNH6 [NCBI] 2.70565e-06
ERG [NCBI] 2.68175e-06
SMN1 [NCBI] 2.64663e-06
KCNQ1 [NCBI] 2.50892e-06
ALDH2 [NCBI] 2.4224e-06
UCP3 [NCBI] 2.41747e-06
SLC11A1 [NCBI] 2.39794e-06
ADRB2 [NCBI] 2.3931e-06
PGF [NCBI] 2.38346e-06
SDC1 [NCBI] 2.33166e-06
SHH [NCBI] 2.33166e-06
NBN [NCBI] 2.31329e-06
CHGA [NCBI] 2.24653e-06
HNF1B [NCBI] 2.22927e-06
NPY [NCBI] 2.21225e-06
HLA-DQA1 [NCBI] 2.19121e-06
LDLR [NCBI] 2.1829e-06
INS [NCBI] 2.14612e-06
MBP [NCBI] 2.13616e-06
HNF1A [NCBI] 2.0986e-06
MEN1 [NCBI] 2.06406e-06
GJB1 [NCBI] 2.05274e-06
LEP [NCBI] 1.98682e-06
F8 [NCBI] 1.97261e-06
MECP2 [NCBI] 1.95159e-06
PKD1 [NCBI] 1.85139e-06
ENG [NCBI] 1.84818e-06
FGFR3 [NCBI] 1.75561e-06
TTR [NCBI] 1.63944e-06
RUNX1 [NCBI] 1.63674e-06
BCR [NCBI] 1.62068e-06
FHIT [NCBI] 1.61273e-06
FLT3 [NCBI] 1.61009e-06
SHBG [NCBI] 1.40097e-06
AR [NCBI] 1.3996e-06
VWF [NCBI] 1.3955e-06
MOG [NCBI] 1.36854e-06
F5 [NCBI] 1.35583e-06
ESR1 [NCBI] 1.23265e-06
BRAF [NCBI] 1.22704e-06
VEGFA [NCBI] 1.14388e-06
HTT [NCBI] 1.12935e-06
APC [NCBI] 8.34476e-07
VDR [NCBI] 8.11589e-07
HLA-DRB1 [NCBI] 6.93814e-07
MSH2 [NCBI] 5.62269e-07
HFE [NCBI] 5.41597e-07
AVP [NCBI] 5.06057e-07
MTHFR [NCBI] 5.02998e-07
PTEN [NCBI] 3.9521e-07
IL1RN [NCBI] 3.40445e-07
BAX [NCBI] 1.19332e-07
FASLG [NCBI] 8.65994e-08



OMIM


 OMIM Link Information
gain		 01
autism [NCBI] 0.00225331
SLI2 [NCBI] 0.00133372
SLI1 [NCBI] 0.00133372
PAND1 [NCBI] 0.00111514
HFM [NCBI] 0.000827778
ANON1 [NCBI] 0.000742313
metatarsus varus, type i [NCBI] 0.000666274
vertebral ossification, defect in, with nephrogenic rests [NCBI] 0.000666274
arteriosclerosis, severe juvenile [NCBI] 0.000666274
bone size quantitative trait locus 1 [NCBI] 0.000666274
synostoses, tarsal, carpal, and digital [NCBI] 0.000666274
exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like [NCBI] 0.000666274
urogenital adysplasia, hereditary [NCBI] 0.000641438
BULN1 [NCBI] 0.000639989
migraine with or without aura, susceptibility to, 1 [NCBI] 0.000592107
chiari malformation type i [NCBI] 0.000592107
RA [NCBI] 0.000570209
ETL2 [NCBI] 0.000506273
constricting bands, congenital [NCBI] 0.000458148
thyroid carcinoma, nonmedullary 1 [NCBI] 0.000450592
3-@hydroxyisobutyric aciduria [NCBI] 0.000450592
necrotizing encephalopathy, acute, autosomal dominant [NCBI] 0.000450592
DYX9 [NCBI] 0.000450592
varadi-papp syndrome [NCBI] 0.000437066
SCZD [NCBI] 0.000391919
MAFD2 [NCBI] 0.000382722
PN [NCBI] 0.000370603
nablus mask-like facial syndrome [NCBI] 0.000370603
cerebellar atrophy with progressive microcephaly [NCBI] 0.000370603
astigmatism [NCBI] 0.000370603
mesomelic dysplasia, kantaputra type [NCBI] 0.000370603
CF [NCBI] 0.00036863
cayler cardiofacial syndrome [NCBI] 0.000325276
coronary heart disease, susceptibility to, 2 [NCBI] 0.000319458
persistent hyperplastic primary vitreous, autosomal recessive [NCBI] 0.000319458
hypertelorism, microtia, facial clefting syndrome [NCBI] 0.000319458
renal-hepatic-pancreatic dysplasia with dandy-walker cyst [NCBI] 0.000319458
MCOPS4 [NCBI] 0.000319458
hernia, hiatus [NCBI] 0.000319458
opioid dependence, susceptibility to, 1 [NCBI] 0.000319458
DYX6 [NCBI] 0.000319458
otitis media, susceptibility to [NCBI] 0.000319458
dermochondrocorneal dystrophy [NCBI] 0.000282011
exstrophy of bladder [NCBI] 0.000282011
mast cell disease [NCBI] 0.000266651
corpus callosum, agenesis of, with facial anomalies and robin sequence [NCBI] 0.000228585
MCOPS6 [NCBI] 0.000228585
hodgkin disease, x-linked pseudoautosomal [NCBI] 0.000228585
wernicke-korsakoff syndrome [NCBI] 0.000228585
BWS [NCBI] 0.000228347
takayasu arteritis [NCBI] 0.000222377
DMD [NCBI] 0.000213739
aneurysm, intracranial berry, 1 [NCBI] 0.000210292
holoprosencephaly [NCBI] 0.000210292
cranioectodermal dysplasia [NCBI] 0.000208328
ocular motor apraxia [NCBI] 0.000208328
popliteal pterygium syndrome, lethal type [NCBI] 0.000208328
letterer-siwe disease [NCBI] 0.000208328
HYPX [NCBI] 0.000190903
cluster headache, familial [NCBI] 0.000190903
amyotrophy, monomelic [NCBI] 0.000175678
PCA [NCBI] 0.000175678
thyroid carcinoma, nonmedullary, with or without cell oxyphilia [NCBI] 0.000175678
MCOP1 [NCBI] 0.000175678
DWS [NCBI] 0.000165676
jejunal atresia [NCBI] 0.00016221
MCOPS1 [NCBI] 0.00016221
short rib-polydactyly syndrome, type iii [NCBI] 0.00016221
basal ganglia calcification, idiopathic, childhood-onset [NCBI] 0.00016221
fanconi renotubular syndrome [NCBI] 0.00016221
TD1 [NCBI] 0.000159485
IDDM [NCBI] 0.0001572
MS [NCBI] 0.00015702
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.000150178
IH [NCBI] 0.000150178
MYMY1 [NCBI] 0.000139342
intestinal atresia, multiple [NCBI] 0.000139342
RSTS [NCBI] 0.000137526
osteochondrosis deformans tibiae, familial infantile type [NCBI] 0.000134527
neuronal intranuclear inclusion disease [NCBI] 0.000134527
chloramphenicol toxicity [NCBI] 0.000134527
fitzsimmons-guilbert syndrome [NCBI] 0.000134527
DYT2 [NCBI] 0.000129518
DYX2 [NCBI] 0.000124236
CDLS1 [NCBI] 0.000123766
SLE [NCBI] 0.000122071
achalasia, familial esophageal [NCBI] 0.00012056
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000114265
FSHMD1A [NCBI] 0.000113203
gastroesophageal reflux [NCBI] 0.000112352
alopecia areata 1 [NCBI] 0.000112352
OFC1 [NCBI] 0.000106716
ACC [NCBI] 0.000104802
anencephaly [NCBI] 0.000104802
WM1 [NCBI] 0.000104802
aromatic l-amino acid decarboxylase deficiency [NCBI] 0.000103869
goodpasture syndrome [NCBI] 0.000103869
barraquer-simons syndrome [NCBI] 0.000103869
hyperthyroidism, nonautoimmune [NCBI] 9.79893e-05
EHBA [NCBI] 9.79893e-05
gastroschisis [NCBI] 9.305e-05
IDD [NCBI] 9.305e-05
DYX1 [NCBI] 9.11101e-05
SCZD9 [NCBI] 8.50558e-05
craniosynostosis with anomalies of the cranial base and digits [NCBI] 8.26767e-05
esophageal ring, lower [NCBI] 8.26767e-05
ectrodactyly-polydactyly [NCBI] 8.26767e-05
cholesterol pneumonia [NCBI] 8.26767e-05
apnea, central sleep [NCBI] 8.26767e-05
asthma, short stature, and elevated iga [NCBI] 8.26767e-05
facial dysmorphism, selective tooth agenesis, and choroid calcification [NCBI] 8.26767e-05
twinning, monozygotic [NCBI] 8.26767e-05
adactylia, unilateral [NCBI] 8.26767e-05
colchicine resistance [NCBI] 8.26767e-05
epiphyseal dysplasia of femoral head, myopia, and deafness [NCBI] 8.26767e-05
hemosiderosis, pulmonary, with deficiency of gamma-a globulin [NCBI] 8.26767e-05
jejunal atresia with renal adysplasia [NCBI] 8.26767e-05
PUPPP [NCBI] 8.26767e-05
breast cancer [NCBI] 8.24167e-05
CDAN2 [NCBI] 7.97968e-05
CPI [NCBI] 7.75374e-05
mucopolysaccharidosis type ii [NCBI] 7.60168e-05
thrombocytopenic purpura, autoimmune [NCBI] 7.23859e-05
GBD1 [NCBI] 7.11859e-05
IHPS1 [NCBI] 7.11859e-05
AD [NCBI] 6.99631e-05
MDD [NCBI] 6.9635e-05
WT1 [NCBI] 6.92372e-05
pituitary dwarfism iii [NCBI] 6.90444e-05
ADHD [NCBI] 6.87938e-05
APC [NCBI] 6.79624e-05
argininosuccinic aciduria [NCBI] 6.70479e-05
bare lymphocyte syndrome, type ii [NCBI] 6.53335e-05
myeloma, multiple [NCBI] 6.51789e-05
anemia, dyserythropoietic congenital, type i [NCBI] 6.51789e-05
dubowitz syndrome [NCBI] 6.51714e-05
RTS [NCBI] 6.37122e-05
GTS [NCBI] 6.2913e-05
RTT [NCBI] 6.13349e-05
VUR1 [NCBI] 6.09028e-05
WFS2 [NCBI] 6.03031e-05
spondylosis, cervical [NCBI] 6.03031e-05
aortic arch interruption, facial palsy, and retinal coloboma [NCBI] 6.03031e-05
myelocytic leukemia-like syndrome, familial, chronic [NCBI] 6.03031e-05
periodontitis, chronic [NCBI] 6.03031e-05
growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction [NCBI] 6.03031e-05
PPAB [NCBI] 6.03031e-05
TSNAX [NCBI] 5.63404e-05
P2RX4 [NCBI] 5.63404e-05
SULT1A1 [NCBI] 5.63404e-05
NPHS1 [NCBI] 5.59632e-05
carnitine palmitoyltransferase ii deficiency, late-onset [NCBI] 5.59632e-05
PPS [NCBI] 5.46814e-05
lung cancer [NCBI] 5.34561e-05
AIC [NCBI] 5.31329e-05
JBTS1 [NCBI] 5.31329e-05
SRS [NCBI] 5.28126e-05
ureterocele [NCBI] 5.192e-05
hydrops fetalis, idiopathic [NCBI] 5.192e-05
coloboma of optic nerve [NCBI] 5.192e-05
MCOPS5 [NCBI] 5.192e-05
sodium-potassium-atpase activity of red cell [NCBI] 5.192e-05
subependymoma [NCBI] 5.192e-05
MCOP3 [NCBI] 5.192e-05
tracheobronchial stenosis, congenital [NCBI] 5.192e-05
keloids [NCBI] 5.192e-05
aarskog syndrome [NCBI] 5.192e-05
bile duct cysts [NCBI] 5.192e-05
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency [NCBI] 5.192e-05
drusen of bruch membrane [NCBI] 5.192e-05
MTHFR [NCBI] 5.14609e-05
PLA2G1B [NCBI] 5.11475e-05
PLXNA2 [NCBI] 5.11475e-05
pulmonary fibrosis, idiopathic [NCBI] 5.00767e-05
PSORS1 [NCBI] 4.73069e-05
fraser syndrome [NCBI] 4.70721e-05
SVAS [NCBI] 4.68052e-05
ovarian teratoma [NCBI] 4.65107e-05
ectopia lentis [NCBI] 4.65107e-05
craniosynostosis with ectopia lentis [NCBI] 4.65107e-05
langerhans cell histiocytosis [NCBI] 4.65107e-05
simpson-golabi-behmel syndrome, type 2 [NCBI] 4.65107e-05
metachondromatosis [NCBI] 4.65107e-05
arachnoid cysts, intracranial [NCBI] 4.65107e-05
say syndrome [NCBI] 4.65107e-05
chylothorax, congenital [NCBI] 4.65107e-05
pars planitis [NCBI] 4.65107e-05
heterotopia, periventricular, ehlers-danlos variant [NCBI] 4.65107e-05
craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis [NCBI] 4.65107e-05
PCD [NCBI] 4.62624e-05
SCDO1 [NCBI] 4.61413e-05
SEPT5 [NCBI] 4.52751e-05
SGBS1 [NCBI] 4.52422e-05
NRCLP1 [NCBI] 4.52422e-05
HD [NCBI] 4.40188e-05
restless legs syndrome, susceptibility to, 1 [NCBI] 4.31254e-05
GPS [NCBI] 4.31254e-05
hypophosphatasia, infantile [NCBI] 4.27171e-05
schindler disease, type i [NCBI] 4.25137e-05
keratitis, hereditary [NCBI] 4.25137e-05
endocardial fibroelastosis [NCBI] 4.25137e-05
MCOP2 [NCBI] 4.25137e-05
respiratory distress syndrome in premature infants [NCBI] 4.25137e-05
hydroxyprolinemia [NCBI] 4.25137e-05
coumarin resistance [NCBI] 4.25137e-05
femur-fibula-ulna syndrome [NCBI] 4.25137e-05
SPDA1 [NCBI] 4.19274e-05
charge syndrome [NCBI] 4.19274e-05
LAMB1 [NCBI] 4.16261e-05
CFD [NCBI] 4.02097e-05
NAGA [NCBI] 4.02097e-05
IL12RB1 [NCBI] 4.02097e-05
SMEI [NCBI] 3.96959e-05
nonarteritic anterior ischemic optic neuropathy, susceptibility to [NCBI] 3.93487e-05
oncocytoma [NCBI] 3.93487e-05
duodenal atresia [NCBI] 3.93487e-05
HPE4 [NCBI] 3.93487e-05
frasier syndrome [NCBI] 3.93487e-05
tibial hemimelia [NCBI] 3.93487e-05
pterygium of conjunctiva and cornea [NCBI] 3.93487e-05
lichen planus, familial [NCBI] 3.93487e-05
HSAN5 [NCBI] 3.93487e-05
native american myopathy [NCBI] 3.93487e-05
FOLR1 [NCBI] 3.89724e-05
HLA-C [NCBI] 3.89724e-05
VEGF [NCBI] 3.87655e-05
RFX5 [NCBI] 3.78741e-05
AMT [NCBI] 3.78741e-05
ALDH1A1 [NCBI] 3.6887e-05
lymphoma, non-hodgkin, familial [NCBI] 3.68005e-05
breath-holding spells [NCBI] 3.67333e-05
porphyria cutanea tarda, type i [NCBI] 3.67333e-05
FHL2 [NCBI] 3.67333e-05
ACHE [NCBI] 3.65483e-05
ZNF9 [NCBI] 3.59906e-05
FGB [NCBI] 3.59906e-05
MBS [NCBI] 3.4755e-05
CDG1A [NCBI] 3.45749e-05
tracheoesophageal fistula with or without esophageal atresia [NCBI] 3.45086e-05
rokitansky-kuster-hauser syndrome [NCBI] 3.45086e-05
asthma, nasal polyps, and aspirin intolerance [NCBI] 3.45086e-05
TD2 [NCBI] 3.45086e-05
bile acid synthesis defect, congenital, 2 [NCBI] 3.45086e-05
lujan-fryns syndrome [NCBI] 3.45086e-05
oeis complex [NCBI] 3.45086e-05
COL11A2 [NCBI] 3.44129e-05
KCNQ1OT1 [NCBI] 3.37109e-05
SLC26A2 [NCBI] 3.37109e-05
KCNQ2 [NCBI] 3.37109e-05
kartagener syndrome [NCBI] 3.34491e-05
MG [NCBI] 3.33943e-05
GK [NCBI] 3.30562e-05
ERCC6 [NCBI] 3.30562e-05
ablepharon-macrostomia syndrome [NCBI] 3.2576e-05
OCA3 [NCBI] 3.2576e-05
TRS [NCBI] 3.2576e-05
atrial septal defect with atrioventricular conduction defects [NCBI] 3.2576e-05
whistling face syndrome, recessive form [NCBI] 3.2576e-05
colloid cysts of third ventricle [NCBI] 3.2576e-05
IRF6 [NCBI] 3.24431e-05
SLC25A20 [NCBI] 3.24431e-05
DISC1 [NCBI] 3.24431e-05
TNF [NCBI] 3.2382e-05
CSA [NCBI] 3.23751e-05
FMR1 [NCBI] 3.21796e-05
CETP [NCBI] 3.18666e-05
krabbe disease [NCBI] 3.13354e-05
SLC22A5 [NCBI] 3.13226e-05
HBG2 [NCBI] 3.13226e-05
cryptorchidism, unilateral or bilateral [NCBI] 3.08701e-05
BPP [NCBI] 3.08701e-05
erythroleukemia, familial [NCBI] 3.08701e-05
acyl-coa dehydrogenase, short-chain, deficiency of [NCBI] 3.08701e-05
sotos syndrome [NCBI] 3.08531e-05
ALDH2 [NCBI] 3.08077e-05
MAOB [NCBI] 3.08077e-05
TYRP1 [NCBI] 3.08077e-05
aHUS [NCBI] 3.03678e-05
DHCR7 [NCBI] 3.0319e-05
MTND5 [NCBI] 3.0319e-05
SCN1A [NCBI] 2.94106e-05
OPLL [NCBI] 2.93454e-05
OSMED [NCBI] 2.93454e-05
amyloidosis vii [NCBI] 2.93454e-05
omphalocele [NCBI] 2.93454e-05
helicobacter pylori infection, susceptibility to [NCBI] 2.93454e-05
shprintzen-goldberg craniosynostosis syndrome [NCBI] 2.93454e-05
macular dystrophy, vitelliform, adult-onset [NCBI] 2.93454e-05
TINU [NCBI] 2.93454e-05
MCOPS9 [NCBI] 2.93454e-05
MKS1 [NCBI] 2.89724e-05
TTR [NCBI] 2.86659e-05
phenylketonuria ii [NCBI] 2.85811e-05
IS1 [NCBI] 2.84153e-05
PWS [NCBI] 2.84009e-05
CBD [NCBI] 2.81919e-05
ALPL [NCBI] 2.81919e-05
VWS [NCBI] 2.80893e-05
oculocerebrocutaneous syndrome [NCBI] 2.79687e-05
pneumothorax, primary spontaneous [NCBI] 2.79687e-05
parkinson disease, mitochondrial [NCBI] 2.79687e-05
XPC [NCBI] 2.78181e-05
ETV6 [NCBI] 2.78181e-05
ICAM1 [NCBI] 2.78181e-05
NBS1 [NCBI] 2.74584e-05
WZS [NCBI] 2.67153e-05
CRS1 [NCBI] 2.67153e-05
disorganization, mouse, homolog of [NCBI] 2.67153e-05
JAG1 [NCBI] 2.64547e-05
aspartylglucosaminuria [NCBI] 2.64547e-05
DDC [NCBI] 2.61426e-05
HRG [NCBI] 2.61426e-05
GSN [NCBI] 2.58404e-05
MTTK [NCBI] 2.58404e-05
DA2B [NCBI] 2.55661e-05
pulmonary alveolar microlithiasis [NCBI] 2.55661e-05
HPE2 [NCBI] 2.55661e-05
MCOPS2 [NCBI] 2.55661e-05
GDXY [NCBI] 2.55477e-05
PIGA [NCBI] 2.52639e-05
NDP [NCBI] 2.49884e-05
FLNA [NCBI] 2.47208e-05
HBD [NCBI] 2.47208e-05
ADLTE [NCBI] 2.45063e-05
OPD1 [NCBI] 2.45063e-05
multiple pterygium syndrome, escobar variant [NCBI] 2.45063e-05
diabetes mellitus, insulin-resistant, with acanthosis nigricans [NCBI] 2.45063e-05
cerebrocostomandibular syndrome [NCBI] 2.45063e-05
PFM [NCBI] 2.45063e-05
myxoma, intracardiac [NCBI] 2.45063e-05
HPE3 [NCBI] 2.45063e-05
leiomyoma, hereditary multiple, of skin [NCBI] 2.35238e-05
COFS1 [NCBI] 2.35238e-05
pitt syndrome [NCBI] 2.35238e-05
kawasaki disease [NCBI] 2.35238e-05
denys-drash syndrome [NCBI] 2.35238e-05
COL7A1 [NCBI] 2.28192e-05
CFTD [NCBI] 2.2609e-05
galactokinase deficiency [NCBI] 2.2609e-05
synovitis, granulomatous, with uveitis and cranial neuropathies [NCBI] 2.2609e-05
infantile spasm syndrome, x-linked [NCBI] 2.2609e-05
autoimmune disease [NCBI] 2.2609e-05
PHA1 [NCBI] 2.2609e-05
OPPG [NCBI] 2.2609e-05
MCOPS3 [NCBI] 2.2609e-05
neuropathy, congenital hypomyelinating [NCBI] 2.2609e-05
F2 [NCBI] 2.21963e-05
MLL [NCBI] 2.21963e-05
MAOA [NCBI] 2.19978e-05
NF1 [NCBI] 2.19695e-05
PEE1 [NCBI] 2.18397e-05
BIRC1 [NCBI] 2.18035e-05
NETH [NCBI] 2.1754e-05
amyloidosis v [NCBI] 2.1754e-05
pycnodysostosis [NCBI] 2.1754e-05
KAL1 [NCBI] 2.16132e-05
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 2.14269e-05
WT1 [NCBI] 2.10652e-05
hypophosphatasia, adult type [NCBI] 2.0952e-05
heart block, congenital [NCBI] 2.0952e-05
MTND4 [NCBI] 2.08897e-05
FA [NCBI] 2.06413e-05
UMS [NCBI] 2.01974e-05
thyroid hormonogenesis, genetic defect in, 2a [NCBI] 2.01974e-05
pena-shokeir syndrome, type i [NCBI] 2.00959e-05
AVSD [NCBI] 1.9991e-05
porphyria cutanea tarda [NCBI] 1.99029e-05
COMT [NCBI] 1.97295e-05
RTD [NCBI] 1.94856e-05
EBN1 [NCBI] 1.94856e-05
ichthyosis congenita, harlequin fetus type [NCBI] 1.94856e-05
IL10 [NCBI] 1.93007e-05
PD [NCBI] 1.91072e-05
stroke, ischemic [NCBI] 1.88124e-05
lymphedema-distichiasis syndrome [NCBI] 1.88124e-05
periodontitis, aggressive, 1 [NCBI] 1.88124e-05
EDMD2 [NCBI] 1.88124e-05
SPCH1 [NCBI] 1.88124e-05
AIS [NCBI] 1.86108e-05
TSC2 [NCBI] 1.86014e-05
PCOS1 [NCBI] 1.84532e-05
AOS [NCBI] 1.84532e-05
MNS [NCBI] 1.81744e-05
GLC3A [NCBI] 1.81744e-05
NBIA1 [NCBI] 1.81744e-05
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency [NCBI] 1.81744e-05
BHD [NCBI] 1.81744e-05
pyruvate carboxylase deficiency [NCBI] 1.81744e-05
COL2A1 [NCBI] 1.77074e-05
CMM2 [NCBI] 1.75684e-05
weaver syndrome [NCBI] 1.75684e-05
thrombocythemia, essential [NCBI] 1.75684e-05
canavan disease [NCBI] 1.69918e-05
hemangioma-thrombocytopenia syndrome [NCBI] 1.69918e-05
ichthyosis, x-linked [NCBI] 1.6897e-05
FGFR1 [NCBI] 1.66788e-05
MRXHF1 [NCBI] 1.64423e-05
diastrophic dysplasia [NCBI] 1.64423e-05
MPZ [NCBI] 1.63617e-05
G6PD [NCBI] 1.59909e-05
hodgkin lymphoma [NCBI] 1.59177e-05
sudden infant death syndrome [NCBI] 1.59177e-05
osteoarthritis [NCBI] 1.59177e-05
AFP [NCBI] 1.57216e-05
OFD1 [NCBI] 1.54162e-05
ETM1 [NCBI] 1.54162e-05
aortic aneurysm, abdominal [NCBI] 1.54162e-05
mucopolysaccharidosis type iiia [NCBI] 1.54162e-05
polycythemia vera [NCBI] 1.54162e-05
HPRT1 [NCBI] 1.49339e-05
INSR [NCBI] 1.47608e-05
mycobacterium tuberculosis, susceptibility to [NCBI] 1.44762e-05
CDK4 [NCBI] 1.41821e-05
CDKN2A [NCBI] 1.41821e-05
hemophagocytic lymphohistiocytosis, familial, 1 [NCBI] 1.40841e-05
CHNG2 [NCBI] 1.40348e-05
leopard syndrome 1 [NCBI] 1.40348e-05
LCA1 [NCBI] 1.40348e-05
PKD1 [NCBI] 1.39462e-05
CFTR [NCBI] 1.39005e-05
autonomic control, congenital failure of [NCBI] 1.36108e-05
HSAS [NCBI] 1.36108e-05
BOR1 [NCBI] 1.36108e-05
MEN1 [NCBI] 1.35678e-05
CASR [NCBI] 1.34942e-05
FCHL [NCBI] 1.32032e-05
MCOPS7 [NCBI] 1.32032e-05
mucopolysaccharidosis type vii [NCBI] 1.32032e-05
megaloblastic anemia 1 [NCBI] 1.32032e-05
MECP2 [NCBI] 1.29974e-05
CEACAM5 [NCBI] 1.28273e-05
OCRL [NCBI] 1.2811e-05
graves disease [NCBI] 1.2811e-05
PPR [NCBI] 1.27998e-05
HBA1 [NCBI] 1.26608e-05
APRT [NCBI] 1.25302e-05
RSMD1 [NCBI] 1.24332e-05
nijmegen breakage syndrome [NCBI] 1.2069e-05
glycogen storage disease v [NCBI] 1.2069e-05
FCAS [NCBI] 1.2069e-05
malaria, susceptibility to [NCBI] 1.2069e-05
CMTX1 [NCBI] 1.2069e-05
MAS [NCBI] 1.19892e-05
testicular tumors [NCBI] 1.17177e-05
SEDC [NCBI] 1.17177e-05
IGER [NCBI] 1.17177e-05
APOE [NCBI] 1.14591e-05
growth hormone insensitivity syndrome [NCBI] 1.13786e-05
RBS [NCBI] 1.13786e-05
CNC1 [NCBI] 1.07344e-05
VHL [NCBI] 1.06886e-05
cardiofaciocutaneous syndrome [NCBI] 1.04282e-05
COH1 [NCBI] 9.84491e-06
obesity [NCBI] 9.84491e-06
campomelic dysplasia [NCBI] 9.84491e-06
COMP [NCBI] 9.70294e-06
PCTT [NCBI] 9.56696e-06
CMD1A [NCBI] 9.56696e-06
BTHS [NCBI] 9.56696e-06
meningioma, familial [NCBI] 9.56696e-06
GCPS [NCBI] 9.29758e-06
SCS [NCBI] 9.29758e-06
VMD [NCBI] 9.29758e-06
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency [NCBI] 9.19236e-06
WFS1 [NCBI] 9.03639e-06
HFE [NCBI] 8.95071e-06
FMF [NCBI] 8.75553e-06
HSAN3 [NCBI] 8.53718e-06
BCR [NCBI] 8.13308e-06
polycystic kidneys [NCBI] 8.03321e-06
thyroid carcinoma, papillary [NCBI] 7.8416e-06
LI1 [NCBI] 7.8416e-06
DYT1 [NCBI] 7.41013e-06
DM2 [NCBI] 7.41013e-06
EIG [NCBI] 7.26714e-06
JPS [NCBI] 7.20333e-06
HNPP [NCBI] 7.00221e-06
BPES [NCBI] 6.80654e-06
CD [NCBI] 6.333e-06
fragile x mental retardation syndrome [NCBI] 6.21758e-06
BRRS [NCBI] 6.07473e-06
osteogenesis imperfecta, type iia [NCBI] 6.07473e-06
ARPKD [NCBI] 5.90363e-06
MHS1 [NCBI] 5.90363e-06
glioma of brain, familial [NCBI] 5.73697e-06
SLC6A3 [NCBI] 5.55921e-06
ALD [NCBI] 5.31269e-06
ARMD1 [NCBI] 5.26216e-06
AS [NCBI] 5.12439e-06
TCOF [NCBI] 4.96533e-06
AMC [NCBI] 4.68318e-06
velocardiofacial syndrome [NCBI] 4.54734e-06
kabuki syndrome [NCBI] 4.45466e-06
GIST [NCBI] 4.43678e-06
PSACH [NCBI] 4.03662e-06
OCP [NCBI] 3.91666e-06
HGPS [NCBI] 3.79963e-06
metachromatic leukodystrophy [NCBI] 3.79963e-06
IBD1 [NCBI] 3.68543e-06
FOP [NCBI] 3.57401e-06
WBS [NCBI] 3.4769e-06
SLS [NCBI] 3.25568e-06
hypogonadotropic hypogonadism [NCBI] 2.95989e-06
WHS [NCBI] 2.34874e-06
alopecia, androgenetic [NCBI] 2.26972e-06
glycogen storage disease ii [NCBI] 2.26972e-06
APOB [NCBI] 2.0286e-06
MFS [NCBI] 1.75398e-06
SCA1 [NCBI] 1.70403e-06
HBB [NCBI] 1.65318e-06
SHBG [NCBI] 1.56259e-06
panencephalitis, subacute sclerosing [NCBI] 1.51559e-06
TS [NCBI] 1.36195e-06
NPY [NCBI] 1.34996e-06
ALPS [NCBI] 1.34968e-06
MBP [NCBI] 1.26433e-06
dystrophia myotonica 1 [NCBI] 1.20044e-06
AR [NCBI] 1.1539e-06
wilson disease [NCBI] 1.09479e-06
CD [NCBI] 8.32553e-07
PJS [NCBI] 7.82811e-07
AVP [NCBI] 6.99438e-07
MODY [NCBI] 6.83867e-07
ACH [NCBI] 6.8194e-07
VDR [NCBI] 6.422e-07
klippel-trenaunay-weber syndrome [NCBI] 5.76201e-07
BBS [NCBI] 4.60732e-07
CMM [NCBI] 4.42338e-07
PMD [NCBI] 3.33027e-07
HSCR1 [NCBI] 2.47597e-07
leber optic atrophy [NCBI] 1.36416e-07
DGS [NCBI] 9.28688e-08
WAS [NCBI] 7.57631e-08
KSS [NCBI] 3.78148e-08
DRPLA [NCBI] 3.10599e-08
PCD [NCBI] 1.10482e-08
LPL [NCBI] 7.51887e-09
BDNF [NCBI] 4.45708e-10



Database Center for Life Science