Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Sex Ratio [NCBI]

Gene


 Gene Link Information
Gain		 01
GRD2 [NCBI] 0.000146274
MA [NCBI] 0.000146274
MS [NCBI] 0.000110704
TRNL1 [NCBI] 8.33687e-05
BRCA2 [NCBI] 6.77826e-06
BRCA1 [NCBI] 6.13274e-06
ACP1 [NCBI] 5.93332e-06
AR [NCBI] 4.76158e-06
CFTR [NCBI] 4.31537e-06
RET [NCBI] 4.19791e-06
FANK1 [NCBI] 3.93227e-06
GPR123 [NCBI] 3.73384e-06
EIF4A2 [NCBI] 3.55823e-06
ADAM8 [NCBI] 3.31142e-06
NOX3 [NCBI] 3.31142e-06
SNX9 [NCBI] 3.1675e-06
PTPRE [NCBI] 3.08328e-06
CNBP [NCBI] 2.91407e-06
GSTT2 [NCBI] 2.88005e-06
TCOF1 [NCBI] 2.84841e-06
DOCK1 [NCBI] 2.81882e-06
LPA [NCBI] 2.74012e-06
L1CAM [NCBI] 2.62856e-06
DTNBP1 [NCBI] 2.53908e-06
EZR [NCBI] 2.50915e-06
CYP21A2 [NCBI] 2.38899e-06
APOA5 [NCBI] 2.32438e-06
U2AF2 [NCBI] 2.31485e-06
SMN2 [NCBI] 2.26572e-06
AMH [NCBI] 2.22527e-06
SMN1 [NCBI] 2.09502e-06
MYOD1 [NCBI] 2.06013e-06
SRY [NCBI] 1.99988e-06
F8 [NCBI] 1.97032e-06
MECP2 [NCBI] 1.88715e-06
PGR [NCBI] 1.86572e-06
CCR5 [NCBI] 1.73043e-06
GSTT1 [NCBI] 1.65247e-06
PTPN11 [NCBI] 1.64335e-06
SNCA [NCBI] 1.62515e-06
GSTM1 [NCBI] 1.56873e-06
ESR1 [NCBI] 1.51907e-06
HFE [NCBI] 1.4549e-06
HLA-DRB1 [NCBI] 1.42861e-06
AFP [NCBI] 1.28341e-06
VIP [NCBI] 1.14473e-06
TNF [NCBI] 5.3979e-07



OMIM


 OMIM Link Information
gain		 01
OFC1 [NCBI] 0.00155183
acetabular dysplasia [NCBI] 0.00130483
OTSC1 [NCBI] 0.00111128
anencephaly [NCBI] 0.00107547
migraine with aura, susceptibility to, 9 [NCBI] 0.00104803
MRX1 [NCBI] 0.000959605
CPL [NCBI] 0.000783606
CPI [NCBI] 0.000749096
pyloric atresia [NCBI] 0.000684289
STUT1 [NCBI] 0.000684289
arima syndrome [NCBI] 0.000684289
graves disease, susceptibility to, 2 [NCBI] 0.000572519
syndactyly, type i [NCBI] 0.000572519
FECD2 [NCBI] 0.000572519
RNANC [NCBI] 0.000534786
trichoepithelioma, multiple familial [NCBI] 0.000534786
AMCN [NCBI] 0.000433204
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.00041483
poland syndrome [NCBI] 0.000398203
MRD [NCBI] 0.000383031
SCZD3 [NCBI] 0.000312739
VUR1 [NCBI] 0.000303456
JBTS1 [NCBI] 0.000303456
diaphragmatic hernia, congenital [NCBI] 0.000286353
myeloproliferative syndrome, transient [NCBI] 0.000256868
urogenital adysplasia, hereditary [NCBI] 0.000201478
SHFM1 [NCBI] 0.000192576
SPD1 [NCBI] 0.000156823
hemophilia a [NCBI] 0.000155822
MEN2B [NCBI] 0.000141731
GLC3A [NCBI] 0.000139697
odontomicronychial dysplasia [NCBI] 0.00013567
exostoses, multiple, type i [NCBI] 0.000123666
autism [NCBI] 0.000116971
mandibulofacial dysostosis, treacher collins type, autosomal recessive [NCBI] 9.74585e-05
RS1 [NCBI] 9.14452e-05
femur-fibula-ulna syndrome [NCBI] 9.06736e-05
clubfoot [NCBI] 9.06736e-05
HAE III [NCBI] 9.06736e-05
chylothorax, congenital [NCBI] 9.06736e-05
RTT [NCBI] 8.94706e-05
pulmonary alveolar microlithiasis [NCBI] 8.56342e-05
RA [NCBI] 8.37842e-05
BWS [NCBI] 8.26776e-05
vacterl association with hydrocephalus [NCBI] 7.82911e-05
hypertriglyceridemia, familial [NCBI] 7.5442e-05
HYR [NCBI] 7.5442e-05
vacterl association with hydrocephalus, x-linked [NCBI] 7.5442e-05
polydactyly, postaxial, type a1 [NCBI] 7.29539e-05
HPRT1 [NCBI] 7.10104e-05
SXI1 [NCBI] 7.07461e-05
hepatitis b virus, susceptibility to [NCBI] 7.07461e-05
IHPS1 [NCBI] 6.69611e-05
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 6.53124e-05
cri-du-chat syndrome [NCBI] 6.37926e-05
HMS1 [NCBI] 6.23832e-05
diarrhea 1, secretory chloride, congenital [NCBI] 5.98392e-05
infantile spasm syndrome, x-linked [NCBI] 5.98392e-05
pituitary dwarfism i [NCBI] 5.86829e-05
MNS [NCBI] 5.86829e-05
CLN2 [NCBI] 5.75921e-05
PPH1 [NCBI] 5.46491e-05
UOX [NCBI] 5.46491e-05
DYX1 [NCBI] 5.13215e-05
HSAS [NCBI] 4.98542e-05
SPDA1 [NCBI] 4.98542e-05
SLE [NCBI] 4.94007e-05
apert syndrome [NCBI] 4.91614e-05
SGBS1 [NCBI] 4.72246e-05
campomelic dysplasia [NCBI] 4.54703e-05
CF [NCBI] 4.54409e-05
BRCA2 [NCBI] 4.10874e-05
aortic valve disease [NCBI] 4.0599e-05
LNS [NCBI] 3.93605e-05
ED1 [NCBI] 3.74695e-05
hurler syndrome [NCBI] 3.71143e-05
NPC1 [NCBI] 3.67661e-05
BPES [NCBI] 3.64246e-05
GTS [NCBI] 3.63043e-05
LQT1 [NCBI] 3.60897e-05
MKS1 [NCBI] 3.60897e-05
HOS [NCBI] 3.5761e-05
TCOF [NCBI] 3.54385e-05
PLUNC [NCBI] 3.53796e-05
APOA5 [NCBI] 3.21267e-05
FACL4 [NCBI] 3.15318e-05
osteogenesis imperfecta, type i [NCBI] 3.14596e-05
SRA2 [NCBI] 3.00388e-05
JARID1D [NCBI] 2.92186e-05
DTNBP1 [NCBI] 2.92186e-05
KCNQ1OT1 [NCBI] 2.84984e-05
TSIX [NCBI] 2.81688e-05
APS1 [NCBI] 2.783e-05
TCOF1 [NCBI] 2.67504e-05
PTPN11 [NCBI] 2.48304e-05
TTR [NCBI] 2.1257e-05
KCNQ1 [NCBI] 2.10656e-05
MTND4 [NCBI] 2.09707e-05
AR [NCBI] 1.88959e-05
ichthyosis, x-linked [NCBI] 1.86691e-05
fragile x mental retardation syndrome [NCBI] 1.76522e-05
DFSP [NCBI] 1.73475e-05
RET [NCBI] 1.64852e-05
leber optic atrophy [NCBI] 1.58321e-05
MECP2 [NCBI] 1.57565e-05
HEMB [NCBI] 1.46251e-05
KCNH2 [NCBI] 1.35556e-05
phenylketonuria [NCBI] 1.34042e-05
dystrophia myotonica 1 [NCBI] 1.29754e-05
AMH [NCBI] 1.23443e-05
PGR [NCBI] 1.0078e-05
HD [NCBI] 7.7389e-06
XDH [NCBI] 7.16297e-06
CFTR [NCBI] 2.53404e-06
AFP [NCBI] 1.90071e-06
CRH [NCBI] 1.17411e-06
CEACAM5 [NCBI] 1.11727e-06
TNF [NCBI] 8.97511e-07
PWS [NCBI] 8.24797e-07
MG [NCBI] 4.15574e-07
thrombocytopenic purpura, autoimmune [NCBI] 2.06928e-08



Database Center for Life Science