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MeSH keywords -> Related genes, diseases (OMIM)


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01 Fetal Death [NCBI]


Gene


Gene Link Information
Gain
01
AFP [NCBI] 0.000138032
MS [NCBI] 5.28348e-05
F2 [NCBI] 3.38878e-05
TROVE2 [NCBI] 3.3643e-05
ACHE [NCBI] 2.86274e-05
KLF1 [NCBI] 2.55771e-05
F5 [NCBI] 2.53542e-05
PIH [NCBI] 2.33746e-05
COL1A1 [NCBI] 2.12911e-05
NR6A1 [NCBI] 2.12625e-05
PROCR [NCBI] 1.98094e-05
HAND1 [NCBI] 1.64875e-05
COL2A1 [NCBI] 1.63277e-05
PROZ [NCBI] 1.63204e-05
EN2 [NCBI] 1.54599e-05
NUP50 [NCBI] 1.39059e-05
ETNK2 [NCBI] 1.39059e-05
FAM179B [NCBI] 1.39059e-05
DHCR7 [NCBI] 1.3566e-05
EPO [NCBI] 1.31214e-05
F2RL3 [NCBI] 1.28494e-05
SHH [NCBI] 1.25191e-05
FOXC2 [NCBI] 1.23083e-05
SOX15 [NCBI] 1.15259e-05
RAB3IP [NCBI] 1.15259e-05
MEP1B [NCBI] 1.15259e-05
CCNF [NCBI] 1.06279e-05
FGB [NCBI] 1.00635e-05
MEP1A [NCBI] 1.00449e-05
MTHFR [NCBI] 9.67081e-06
TFEC [NCBI] 9.61156e-06
RALY [NCBI] 9.61156e-06
PRPF19 [NCBI] 9.61156e-06
LSM4 [NCBI] 9.61156e-06
CD68 [NCBI] 9.25782e-06
NUP153 [NCBI] 8.97931e-06
NPHP3 [NCBI] 8.97931e-06
ALPP [NCBI] 8.97931e-06
FGFR2 [NCBI] 8.80778e-06
BIRC6 [NCBI] 8.73368e-06
MKS1 [NCBI] 8.32832e-06
FKBP1A [NCBI] 8.32832e-06
BMP4 [NCBI] 8.2655e-06
RAB8A [NCBI] 8.15684e-06
RB1CC1 [NCBI] 8.15684e-06
POMT1 [NCBI] 7.8583e-06
CCNB2 [NCBI] 7.8583e-06
LGALS13 [NCBI] 7.8583e-06
JAK2 [NCBI] 7.82453e-06
FLT1 [NCBI] 7.72661e-06
ADSL [NCBI] 7.7266e-06
TTK [NCBI] 7.60436e-06
TFEB [NCBI] 7.38345e-06
IKBKE [NCBI] 7.36412e-06
PLCB3 [NCBI] 7.2829e-06
HTRA2 [NCBI] 7.2829e-06
PGF [NCBI] 7.1097e-06
DLAT [NCBI] 7.09807e-06
AGTR1 [NCBI] 7.06925e-06
CHUK [NCBI] 7.02932e-06
THRA [NCBI] 7.0127e-06
IKBKB [NCBI] 7.00954e-06
TEAD1 [NCBI] 6.93142e-06
SPTB [NCBI] 6.85386e-06
INVS [NCBI] 6.85386e-06
MEF2C [NCBI] 6.85386e-06
HAND2 [NCBI] 6.85386e-06
FXR2 [NCBI] 6.85386e-06
PAX1 [NCBI] 6.7797e-06
ZIC2 [NCBI] 6.70865e-06
ELL [NCBI] 6.64047e-06
CUL4A [NCBI] 6.33559e-06
CPT2 [NCBI] 6.33559e-06
TRAF2 [NCBI] 6.2807e-06
KCNH1 [NCBI] 6.22756e-06
CENPC1 [NCBI] 6.17603e-06
C5AR1 [NCBI] 5.98442e-06
LAMC1 [NCBI] 5.98442e-06
ENG [NCBI] 5.96021e-06
FES [NCBI] 5.85382e-06
ASAH1 [NCBI] 5.81245e-06
ASPA [NCBI] 5.65652e-06
SPTA1 [NCBI] 5.65652e-06
FLNA [NCBI] 5.61971e-06
FLI1 [NCBI] 5.58369e-06
KLF6 [NCBI] 5.51391e-06
RUNX1 [NCBI] 5.49617e-06
ITGA3 [NCBI] 5.48008e-06
CCRK [NCBI] 5.44693e-06
PAX9 [NCBI] 5.44693e-06
CDK7 [NCBI] 5.35127e-06
XRCC2 [NCBI] 5.29042e-06
TAGLN [NCBI] 5.26082e-06
MAP3K5 [NCBI] 5.26082e-06
TLX1 [NCBI] 5.23173e-06
GATA2 [NCBI] 5.17505e-06
HAPLN1 [NCBI] 5.14742e-06
CYP2C8 [NCBI] 5.14742e-06
NCOA2 [NCBI] 5.14742e-06
ATRX [NCBI] 5.12024e-06
SOX2 [NCBI] 4.99069e-06
NOTCH4 [NCBI] 4.99069e-06
BRCA2 [NCBI] 4.9496e-06
PODXL [NCBI] 4.94159e-06
CHM [NCBI] 4.94159e-06
TSG101 [NCBI] 4.89392e-06
REN [NCBI] 4.89392e-06
ADAR [NCBI] 4.87059e-06
THBD [NCBI] 4.84758e-06
TFE3 [NCBI] 4.80253e-06
A2M [NCBI] 4.78045e-06
LIF [NCBI] 4.77313e-06
SRF [NCBI] 4.71596e-06
DKC1 [NCBI] 4.69502e-06
ANGPT2 [NCBI] 4.67434e-06
GLI3 [NCBI] 4.61383e-06
MARCKS [NCBI] 4.48081e-06
IL1B [NCBI] 4.34205e-06
TFPI2 [NCBI] 4.21242e-06
SGK1 [NCBI] 4.19705e-06
FMR1 [NCBI] 4.17383e-06
F13A1 [NCBI] 4.12229e-06
F3 [NCBI] 4.03696e-06
PAX2 [NCBI] 4.0095e-06
MST1R [NCBI] 3.99595e-06
FOSL1 [NCBI] 3.98251e-06
EPOR [NCBI] 3.95596e-06
MYOD1 [NCBI] 3.8789e-06
KCNH2 [NCBI] 3.85402e-06
GFAP [NCBI] 3.75271e-06
TSC2 [NCBI] 3.74668e-06
RUNX1T1 [NCBI] 3.74668e-06
SOX9 [NCBI] 3.7352e-06
FAH [NCBI] 3.70123e-06
CASP9 [NCBI] 3.64603e-06
DIABLO [NCBI] 3.58264e-06
PIGA [NCBI] 3.51162e-06
SOCS1 [NCBI] 3.4155e-06
TG [NCBI] 3.36138e-06
CDKN1C [NCBI] 3.35161e-06
CDX2 [NCBI] 3.32502e-06
KLRK1 [NCBI] 3.26473e-06
JAG1 [NCBI] 3.23131e-06
SRY [NCBI] 3.23131e-06
NAT1 [NCBI] 3.21488e-06
MITF [NCBI] 3.16661e-06
SOCS3 [NCBI] 3.14305e-06
FADD [NCBI] 3.05231e-06
FGF7 [NCBI] 2.98769e-06
TNF [NCBI] 2.96345e-06
CREBBP [NCBI] 2.85986e-06
DAG1 [NCBI] 2.85986e-06
IL6 [NCBI] 2.81921e-06
IGF2 [NCBI] 2.80919e-06
GRP [NCBI] 2.78449e-06
CXCR4 [NCBI] 2.74822e-06
FXN [NCBI] 2.74226e-06
LBP [NCBI] 2.63901e-06
ARID4A [NCBI] 2.62249e-06
ITGB3 [NCBI] 2.58469e-06
AMBP [NCBI] 2.57407e-06
CYP2C9 [NCBI] 2.57407e-06
TNFRSF10A [NCBI] 2.52725e-06
RAD51 [NCBI] 2.50692e-06
ERBB4 [NCBI] 2.48689e-06
XRCC5 [NCBI] 2.39544e-06
PTPN11 [NCBI] 2.34962e-06
IL1A [NCBI] 2.34064e-06
AHR [NCBI] 2.33617e-06
IL1RN [NCBI] 2.31733e-06
XIAP [NCBI] 2.25389e-06
RAG1 [NCBI] 2.14494e-06
LAMB3 [NCBI] 2.1257e-06
MEN1 [NCBI] 2.12188e-06
CDKN1B [NCBI] 2.11808e-06
TFPI [NCBI] 2.07694e-06
LEP [NCBI] 2.04421e-06
FOLR1 [NCBI] 2.02993e-06
MECP2 [NCBI] 2.00878e-06
MCL1 [NCBI] 1.9777e-06
CDKN2B [NCBI] 1.9407e-06
DHFR [NCBI] 1.76168e-06
SERPINE1 [NCBI] 1.61048e-06
ACP5 [NCBI] 1.49926e-06
APOB [NCBI] 1.40426e-06
MLL [NCBI] 1.40003e-06
PTGS1 [NCBI] 1.20383e-06
HTT [NCBI] 1.17957e-06
CXCL12 [NCBI] 1.09899e-06
ADA [NCBI] 1.08957e-06
PCNA [NCBI] 1.035e-06
IL10 [NCBI] 9.19891e-07
VIP [NCBI] 9.08269e-07
ACE [NCBI] 7.7345e-07
CASP3 [NCBI] 7.58105e-07
HRAS [NCBI] 6.88936e-07
MSH2 [NCBI] 6.02804e-07
TH [NCBI] 5.94248e-07
HFE [NCBI] 5.8162e-07
NOS3 [NCBI] 4.78881e-07
MBP [NCBI] 3.46458e-07
EGF [NCBI] 2.60203e-07
BAX [NCBI] 1.41799e-07
VEGFA [NCBI] 6.44848e-08
PRL [NCBI] 3.76294e-08
PTGS2 [NCBI] 3.4905e-08
PTH [NCBI] 3.40724e-08
APOE [NCBI] 1.92088e-08




OMIM


OMIM Link Information
gain
01
FRNS [NCBI] 0.00144739
ACG1A [NCBI] 0.0012838
urogenital adysplasia, hereditary [NCBI] 0.00118971
short rib-polydactyly syndrome, type i [NCBI] 0.00097863
cardiomyopathy, fatal fetal, due to myocardial calcification [NCBI] 0.000814853
pena-shokeir syndrome, type i [NCBI] 0.00080975
multiple pterygium syndrome, lethal type [NCBI] 0.000769156
megacystis-microcolon-intestinal hypoperistalsis syndrome [NCBI] 0.000740364
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.000626032
osteodysplasia, familial, anderson type [NCBI] 0.00059777
NLS [NCBI] 0.000544841
PCD [NCBI] 0.000511773
holoprosencephaly [NCBI] 0.000464399
campomelia, cumming type [NCBI] 0.000463831
renal-hepatic-pancreatic dysplasia with dandy-walker cyst [NCBI] 0.000463831
patent ductus arteriosus [NCBI] 0.000463831
spondylometaphyseal dysplasia, sedaghatian type [NCBI] 0.000424981
opsismodysplasia [NCBI] 0.000424981
MKS2 [NCBI] 0.0003942
lethal congenital contracture syndrome 1 [NCBI] 0.0003942
metatropic dwarfism [NCBI] 0.00036875
popliteal pterygium syndrome, lethal type [NCBI] 0.000347089
dyssegmental dysplasia, rolland-desbuquois type [NCBI] 0.000347089
RA [NCBI] 0.000327624
renal hamartomas, nephroblastomatosis, and fetal gigantism [NCBI] 0.000311633
AFP [NCBI] 0.000307184
OFD4 [NCBI] 0.000296762
short rib-polydactyly syndrome, type iii [NCBI] 0.000296762
SHFLD1 [NCBI] 0.000283326
short rib-polydactyly syndrome, type iv [NCBI] 0.000271087
AMCN [NCBI] 0.000259858
constricting bands, congenital [NCBI] 0.000259858
SLE [NCBI] 0.000243032
short rib-polydactyly syndrome, type ii [NCBI] 0.000239884
gracile bone dysplasia [NCBI] 0.00023161
anencephaly [NCBI] 0.000230929
marden-walker syndrome [NCBI] 0.000222553
CPI [NCBI] 0.000211716
fraser syndrome [NCBI] 0.000204252
por deficiency [NCBI] 0.000200142
diaphragmatic hernia, congenital [NCBI] 0.000181464
ACG2 [NCBI] 0.000181386
CF [NCBI] 0.00017117
RTD [NCBI] 0.000159933
PLSDT [NCBI] 0.000137427
POR [NCBI] 0.000128418
HAND1 [NCBI] 0.000125975
BOCD [NCBI] 0.000118357
PEE1 [NCBI] 0.000117031
KLF1 [NCBI] 0.000116903
pseudotrisomy 13 syndrome [NCBI] 0.000114963
antiphospholipid syndrome [NCBI] 0.000111898
DWS [NCBI] 0.000110828
AOS [NCBI] 0.000110828
MKS1 [NCBI] 0.000107807
heterotopia, periventricular, x-linked dominant [NCBI] 9.99001e-05
lethal short-limb skeletal dysplasia, al gazali type [NCBI] 9.95569e-05
multiple congenital anomalies syndrome with cloverleaf skull [NCBI] 9.95569e-05
fibuloulnar aplasia or hypoplasia with renal abnormalities [NCBI] 9.95569e-05
osteogenesis imperfecta, sillence type ii/iii, without abnormality of type i collagen [NCBI] 9.95569e-05
baby rattle pelvis dysplasia [NCBI] 9.95569e-05
blood group--en [NCBI] 9.95569e-05
TFAM [NCBI] 9.84483e-05
F2RL3 [NCBI] 9.84483e-05
TD1 [NCBI] 9.47823e-05
NR6A1 [NCBI] 9.25763e-05
GSC [NCBI] 8.80805e-05
PROCR [NCBI] 8.69484e-05
hypertelorism with esophageal abnormality and hypospadias [NCBI] 8.2737e-05
SLOS [NCBI] 8.17943e-05
FOLR1 [NCBI] 7.87067e-05
crane-heise syndrome [NCBI] 7.7119e-05
craniomicromelic syndrome [NCBI] 7.7119e-05
contractures, congenital, torticollis, and malignant hyperthermia [NCBI] 7.7119e-05
thymic-renal-anal-lung dysplasia [NCBI] 7.7119e-05
POMT1 [NCBI] 7.06867e-05
multiple pterygium syndrome, aslan type [NCBI] 6.86717e-05
BDA6 [NCBI] 6.86717e-05
osteopetrosis and infantile neuroaxonal dystrophy [NCBI] 6.86717e-05
pterygium syndrome, multiple, x-linked [NCBI] 6.86717e-05
chylothorax, congenital [NCBI] 6.31982e-05
DDSH [NCBI] 6.31982e-05
aminopterin syndrome sine aminopterin [NCBI] 6.31982e-05
PELO [NCBI] 6.29681e-05
ESRRB [NCBI] 6.29681e-05
FKBP1A [NCBI] 6.29681e-05
IGKV1OR2108 [NCBI] 6.29681e-05
CCNB2 [NCBI] 6.29681e-05
MAP3K7IP2 [NCBI] 6.29681e-05
ROCK2 [NCBI] 6.29681e-05
MEP1B [NCBI] 6.29681e-05
GCN5L2 [NCBI] 6.29681e-05
BWS [NCBI] 6.18687e-05
pulmonary hypertension, familial persistent, of the newborn [NCBI] 5.91371e-05
aprosencephaly syndrome [NCBI] 5.91371e-05
malpuech facial clefting syndrome [NCBI] 5.91371e-05
osteogenesis imperfecta, type iia [NCBI] 5.90629e-05
COL1A1 [NCBI] 5.67732e-05
isotretinoin embryopathy-like syndrome [NCBI] 5.59078e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 5.59078e-05
weyers ulnar ray/oligodactyly syndrome [NCBI] 5.59078e-05
IKBKG [NCBI] 5.41032e-05
schneckenbecken dysplasia [NCBI] 5.32282e-05
BMP4 [NCBI] 5.21315e-05
murcs association [NCBI] 5.09393e-05
carnitine palmitoyltransferase ii deficiency, lethal neonatal [NCBI] 5.09393e-05
boomerang dysplasia [NCBI] 5.09393e-05
oeis complex [NCBI] 5.09393e-05
MTHFD2 [NCBI] 4.92049e-05
PLOD3 [NCBI] 4.92049e-05
STE [NCBI] 4.92049e-05
TRRAP [NCBI] 4.92049e-05
ADRA2A [NCBI] 4.92049e-05
TNS1 [NCBI] 4.92049e-05
ATP5A1 [NCBI] 4.92049e-05
BIRC6 [NCBI] 4.92049e-05
TXN2 [NCBI] 4.92049e-05
TPST1 [NCBI] 4.92049e-05
MGAT1 [NCBI] 4.92049e-05
CUL1 [NCBI] 4.92049e-05
PRMT1 [NCBI] 4.92049e-05
ICMT [NCBI] 4.92049e-05
ablepharon-macrostomia syndrome [NCBI] 4.89425e-05
blood group, p system [NCBI] 4.89425e-05
AVSD [NCBI] 4.84752e-05
BPP [NCBI] 4.71724e-05
MCOPS9 [NCBI] 4.55835e-05
MRXS13 [NCBI] 4.41426e-05
hydrolethalus syndrome 1 [NCBI] 4.41426e-05
AOI [NCBI] 4.41426e-05
TEAD1 [NCBI] 4.40211e-05
ITGA6 [NCBI] 4.40211e-05
HTR2B [NCBI] 4.40211e-05
IDH3G [NCBI] 4.40211e-05
GRIP1 [NCBI] 4.40211e-05
NR2C2 [NCBI] 4.40211e-05
ACHE [NCBI] 4.35345e-05
LQT3 [NCBI] 4.2825e-05
hydrocephalus [NCBI] 4.2825e-05
vitamin k-dependent clotting factors, combined deficiency of, 1 [NCBI] 4.16116e-05
HPE2 [NCBI] 4.16116e-05
hemochromatosis, neonatal [NCBI] 4.16116e-05
NR5A2 [NCBI] 4.06609e-05
CCNB1 [NCBI] 4.06609e-05
ATOX1 [NCBI] 4.06609e-05
DLAT [NCBI] 4.06609e-05
LAMC1 [NCBI] 4.06609e-05
XRCC5 [NCBI] 4.06609e-05
EFEMP2 [NCBI] 4.06609e-05
MCL1 [NCBI] 4.06609e-05
GATA2 [NCBI] 4.06609e-05
rad54, s. cerevisiae, homolog of, b [NCBI] 4.06609e-05
multiple pterygium syndrome, escobar variant [NCBI] 4.04875e-05
caffey disease [NCBI] 4.04875e-05
PTH [NCBI] 3.97382e-05
chondrodysplasia punctata, autosomal dominant [NCBI] 3.94409e-05
COFS1 [NCBI] 3.94409e-05
tetralogy of fallot [NCBI] 3.94409e-05
CDLS1 [NCBI] 3.912e-05
afibrinogenemia, congenital [NCBI] 3.84619e-05
MAPK9 [NCBI] 3.81668e-05
NCOA6 [NCBI] 3.81668e-05
A4GALT [NCBI] 3.81668e-05
MST1R [NCBI] 3.81668e-05
ITPR1 [NCBI] 3.81668e-05
MARCKS [NCBI] 3.81668e-05
MTHFR [NCBI] 3.77196e-05
papillorenal syndrome [NCBI] 3.75426e-05
CDPX1 [NCBI] 3.66764e-05
CDX2 [NCBI] 3.61828e-05
FADD [NCBI] 3.61828e-05
XBP1 [NCBI] 3.61828e-05
factor v deficiency [NCBI] 3.50901e-05
IP [NCBI] 3.46567e-05
FBXW7 [NCBI] 3.45358e-05
CITED2 [NCBI] 3.45358e-05
CCNA2 [NCBI] 3.45358e-05
ZIC2 [NCBI] 3.45358e-05
TFAP2A [NCBI] 3.45358e-05
SCN2A [NCBI] 3.45358e-05
BCAR1 [NCBI] 3.45358e-05
SFTPD [NCBI] 3.45358e-05
LAMB1 [NCBI] 3.45358e-05
lymphedema-distichiasis syndrome [NCBI] 3.43442e-05
MAP2K1 [NCBI] 3.31285e-05
JUN [NCBI] 3.31285e-05
IGF2R [NCBI] 3.31285e-05
PEG3 [NCBI] 3.31285e-05
BARD1 [NCBI] 3.31285e-05
DLL4 [NCBI] 3.31285e-05
TRAF2 [NCBI] 3.31285e-05
PAPPA [NCBI] 3.31285e-05
MEST [NCBI] 3.31285e-05
ECE1 [NCBI] 3.31285e-05
GBA [NCBI] 3.3023e-05
HSS [NCBI] 3.29717e-05
ADSL [NCBI] 3.19003e-05
MAPK7 [NCBI] 3.19003e-05
PLCB3 [NCBI] 3.19003e-05
epidermolysis bullosa with pyloric atresia [NCBI] 3.11284e-05
THBD [NCBI] 3.08111e-05
RELA [NCBI] 3.08111e-05
MT1A [NCBI] 3.08111e-05
GSK3B [NCBI] 3.08111e-05
central core disease of muscle [NCBI] 3.00185e-05
FLI1 [NCBI] 2.9833e-05
SIRT1 [NCBI] 2.9833e-05
LIG4 [NCBI] 2.9833e-05
MST1 [NCBI] 2.9833e-05
CREB1 [NCBI] 2.9833e-05
EGF [NCBI] 2.97395e-05
OKS [NCBI] 2.94942e-05
ABS [NCBI] 2.94942e-05
MKKS [NCBI] 2.89886e-05
MAPK8 [NCBI] 2.89456e-05
GATA3 [NCBI] 2.89456e-05
LDHA [NCBI] 2.89456e-05
TSG101 [NCBI] 2.89456e-05
HSAS [NCBI] 2.85004e-05
E2F1 [NCBI] 2.81339e-05
CPT2 [NCBI] 2.81339e-05
pfeiffer syndrome [NCBI] 2.80286e-05
SGBS1 [NCBI] 2.75721e-05
DGS [NCBI] 2.69511e-05
CBFA2T1 [NCBI] 2.66931e-05
hypophosphatasia, infantile [NCBI] 2.62862e-05
TBS [NCBI] 2.62862e-05
CDPX2 [NCBI] 2.62862e-05
SEDC [NCBI] 2.62862e-05
apert syndrome [NCBI] 2.62862e-05
GK [NCBI] 2.60475e-05
CASP8 [NCBI] 2.60475e-05
MEB [NCBI] 2.58829e-05
LIFR [NCBI] 2.54434e-05
CXCR4 [NCBI] 2.54434e-05
TPT1 [NCBI] 2.54434e-05
walker-warburg syndrome [NCBI] 2.47398e-05
MAP1B [NCBI] 2.4341e-05
FOXC2 [NCBI] 2.4341e-05
KLF6 [NCBI] 2.4341e-05
TRPS2 [NCBI] 2.4028e-05
campomelic dysplasia [NCBI] 2.4028e-05
DKC1 [NCBI] 2.38352e-05
3-@hydroxy-3-methylglutaryl-coa lyase deficiency [NCBI] 2.33556e-05
DHCR7 [NCBI] 2.33556e-05
NOTCH1 [NCBI] 2.33556e-05
FDH [NCBI] 2.33522e-05
SPTB [NCBI] 2.28996e-05
ATR [NCBI] 2.28996e-05
PRL [NCBI] 2.26036e-05
EDN1 [NCBI] 2.24653e-05
PAX2 [NCBI] 2.24653e-05
H19 [NCBI] 2.24653e-05
SOCS1 [NCBI] 2.24653e-05
FGG [NCBI] 2.24653e-05
ADM [NCBI] 2.19795e-05
ALPL [NCBI] 2.12737e-05
CHM [NCBI] 2.06799e-05
NBS1 [NCBI] 2.05583e-05
FCMD [NCBI] 1.99e-05
TNF [NCBI] 1.98713e-05
SOCS3 [NCBI] 1.92787e-05
F3 [NCBI] 1.90784e-05
HOS [NCBI] 1.89305e-05
MFS [NCBI] 1.87818e-05
MG [NCBI] 1.87423e-05
RECQL2 [NCBI] 1.8702e-05
PDHA1 [NCBI] 1.8702e-05
ASPA [NCBI] 1.79022e-05
FLNA [NCBI] 1.79022e-05
ENG [NCBI] 1.76511e-05
F2R [NCBI] 1.74071e-05
coproporphyria [NCBI] 1.74071e-05
AMC [NCBI] 1.71961e-05
ATRX [NCBI] 1.71698e-05
RUNX1 [NCBI] 1.71698e-05
MTATP6 [NCBI] 1.71698e-05
A2M [NCBI] 1.6495e-05
factor x deficiency [NCBI] 1.62814e-05
F2 [NCBI] 1.54774e-05
NOS3 [NCBI] 1.51026e-05
factor vii deficiency [NCBI] 1.51026e-05
SCN5A [NCBI] 1.47441e-05
FXN [NCBI] 1.47441e-05
osteogenesis imperfecta, type i [NCBI] 1.43509e-05
PKD2 [NCBI] 1.4071e-05
thrombocytopenic purpura, autoimmune [NCBI] 1.40641e-05
menkes disease [NCBI] 1.40414e-05
glycogen storage disease i [NCBI] 1.36006e-05
thrombasthenia of glanzmann and naegeli [NCBI] 1.35933e-05
MAP3K5 [NCBI] 1.34497e-05
LS [NCBI] 1.31634e-05
RYR1 [NCBI] 1.26004e-05
LBP [NCBI] 1.26004e-05
CPB2 [NCBI] 1.24674e-05
cortisol 11-beta-ketoreductase deficiency [NCBI] 1.22081e-05
TSC2 [NCBI] 1.20816e-05
SRF [NCBI] 1.14792e-05
COL2A1 [NCBI] 1.12511e-05
VHL [NCBI] 1.11396e-05
SHH [NCBI] 1.04463e-05
FRDA [NCBI] 1.02607e-05
EPOR [NCBI] 1.00141e-05
PCNA [NCBI] 9.93869e-06
NPM1 [NCBI] 9.64519e-06
JAK2 [NCBI] 9.3808e-06
ABCG2 [NCBI] 9.12622e-06
DNMT1 [NCBI] 8.49101e-06
MBP [NCBI] 7.79988e-06
MEN1 [NCBI] 7.51013e-06
BRCA2 [NCBI] 7.31858e-06
CMH [NCBI] 7.22307e-06
MECP2 [NCBI] 7.01222e-06
FGFR2 [NCBI] 6.66438e-06
apc gene [NCBI] 5.82923e-06
VEGF [NCBI] 5.6045e-06
TSD [NCBI] 4.77115e-06
GPI [NCBI] 4.74255e-06
TH [NCBI] 4.55396e-06
WBS [NCBI] 4.48303e-06
EPO [NCBI] 4.30105e-06
TS [NCBI] 4.25806e-06
PPARA [NCBI] 3.93129e-06
BRCA1 [NCBI] 3.76503e-06
phenylketonuria [NCBI] 3.1593e-06
RB1 [NCBI] 3.05433e-06
dystrophia myotonica 1 [NCBI] 3.03812e-06
VIP [NCBI] 1.64987e-06
AHR [NCBI] 1.55655e-06
GNRH1 [NCBI] 1.07796e-06
GFAP [NCBI] 1.05107e-06
HGF [NCBI] 1.04145e-06
panencephalitis, subacute sclerosing [NCBI] 7.99603e-07
ADA [NCBI] 7.648e-07
TFPI [NCBI] 5.12862e-07
MUC1 [NCBI] 4.47724e-07
G6PD [NCBI] 1.3393e-07
HD [NCBI] 1.21953e-07
DHFR [NCBI] 6.89655e-08
TG [NCBI] 5.06297e-08
APOB [NCBI] 9.69218e-11




Database Center for Life Science