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01 Twins [NCBI]

Gene


 Gene Link Information
Gain		 01
MS [NCBI] 0.000317265
SLI2 [NCBI] 0.000161136
SLI1 [NCBI] 0.000161136
STQTL2 [NCBI] 0.000135859
HFM [NCBI] 8.97433e-05
AFP [NCBI] 5.77753e-05
DRD4 [NCBI] 1.86102e-05
TFPI2 [NCBI] 1.81338e-05
PIH [NCBI] 1.26688e-05
SLC6A3 [NCBI] 1.15492e-05
OCA2 [NCBI] 7.35368e-06
DISC1 [NCBI] 6.97751e-06
FMR1 [NCBI] 6.39892e-06
KIAA0319 [NCBI] 5.84441e-06
SLC6A4 [NCBI] 5.35196e-06
APOE [NCBI] 3.97712e-06
IGFBP1 [NCBI] 3.74179e-06
MTHFR [NCBI] 3.67797e-06
CHGA [NCBI] 3.49843e-06
USP12 [NCBI] 3.00778e-06
LDLR [NCBI] 3.00595e-06
NDUFB6 [NCBI] 2.96223e-06
SLCO1C1 [NCBI] 2.96223e-06
TTRAP [NCBI] 2.88289e-06
PARK2 [NCBI] 2.85019e-06
SLC4A7 [NCBI] 2.78503e-06
SHC2 [NCBI] 2.7566e-06
RARS [NCBI] 2.70457e-06
GLS [NCBI] 2.6579e-06
VPS33B [NCBI] 2.6579e-06
INSL4 [NCBI] 2.59581e-06
HERC2 [NCBI] 2.57687e-06
SOX1 [NCBI] 2.55869e-06
TSNAX [NCBI] 2.54121e-06
MEST [NCBI] 2.50814e-06
AVPR1A [NCBI] 2.46267e-06
HLTF [NCBI] 2.42134e-06
COMT [NCBI] 2.40881e-06
NNMT [NCBI] 2.38347e-06
PPARGC1B [NCBI] 2.35987e-06
SEPT5 [NCBI] 2.34852e-06
GAL [NCBI] 2.29567e-06
BSCL2 [NCBI] 2.24834e-06
HFE [NCBI] 2.20923e-06
CHRNA4 [NCBI] 2.12348e-06
S100A12 [NCBI] 2.11004e-06
DAOA [NCBI] 2.097e-06
NAMPT [NCBI] 2.0781e-06
SFTPD [NCBI] 2.0781e-06
GCH1 [NCBI] 2.04254e-06
NDP [NCBI] 2.03128e-06
HSPA1B [NCBI] 2.00957e-06
HRG [NCBI] 1.95476e-06
CSF1 [NCBI] 1.9409e-06
ABO [NCBI] 1.89345e-06
PPARD [NCBI] 1.88533e-06
CNR1 [NCBI] 1.87343e-06
DTNBP1 [NCBI] 1.86567e-06
CYP2A6 [NCBI] 1.85426e-06
SLC2A3 [NCBI] 1.82874e-06
HBA2 [NCBI] 1.78166e-06
DDC [NCBI] 1.75986e-06
IKBKG [NCBI] 1.70284e-06
MC1R [NCBI] 1.68192e-06
TCF7L2 [NCBI] 1.67937e-06
XRCC3 [NCBI] 1.67432e-06
MTR [NCBI] 1.67182e-06
PAFAH1B1 [NCBI] 1.66933e-06
GC [NCBI] 1.66194e-06
GH1 [NCBI] 1.65708e-06
FGB [NCBI] 1.65467e-06
HSPA1A [NCBI] 1.63585e-06
NRG1 [NCBI] 1.58578e-06
MSTN [NCBI] 1.5716e-06
MAGEA3 [NCBI] 1.54265e-06
FGFR1 [NCBI] 1.54078e-06
VWF [NCBI] 1.53922e-06
PSMB8 [NCBI] 1.52256e-06
HBA1 [NCBI] 1.5085e-06
BDNF [NCBI] 1.50272e-06
EPO [NCBI] 1.48117e-06
SIRT1 [NCBI] 1.47519e-06
PSMB9 [NCBI] 1.45328e-06
PIK3R1 [NCBI] 1.43827e-06
ACHE [NCBI] 1.42093e-06
CRH [NCBI] 1.41388e-06
PAEP [NCBI] 1.40558e-06
FLT1 [NCBI] 1.38549e-06
STAR [NCBI] 1.3726e-06
WRN [NCBI] 1.37006e-06
DBH [NCBI] 1.3688e-06
SCGB1A1 [NCBI] 1.33255e-06
SRY [NCBI] 1.33139e-06
PGF [NCBI] 1.32223e-06
IGF2 [NCBI] 1.31216e-06
DRD2 [NCBI] 1.30123e-06
WAS [NCBI] 1.26999e-06
ADRB2 [NCBI] 1.23711e-06
CFTR [NCBI] 1.21795e-06
PKD1 [NCBI] 1.20917e-06
RELN [NCBI] 1.20742e-06
TAP2 [NCBI] 1.19542e-06
SLC2A4 [NCBI] 1.11194e-06
IGF1 [NCBI] 1.08694e-06
SLC2A1 [NCBI] 1.07402e-06
XRCC5 [NCBI] 1.05536e-06
MLL [NCBI] 1.05232e-06
TTR [NCBI] 1.05172e-06
TAP1 [NCBI] 1.03111e-06
GSTT1 [NCBI] 9.92177e-07
PTPN11 [NCBI] 9.83371e-07
TF [NCBI] 9.7676e-07
PTGS1 [NCBI] 9.47075e-07
CETP [NCBI] 9.1415e-07
GSTM1 [NCBI] 9.11558e-07
APOB [NCBI] 9.04725e-07
IL10 [NCBI] 8.56087e-07
ACE [NCBI] 8.14723e-07
TRH [NCBI] 6.49427e-07
CAT [NCBI] 6.25936e-07
NOS3 [NCBI] 6.07974e-07
LPL [NCBI] 5.97302e-07
EGF [NCBI] 5.42773e-07
VEGFA [NCBI] 5.09852e-07
AR [NCBI] 4.64401e-07
PTGS2 [NCBI] 3.55259e-07
CDKN1A [NCBI] 3.0055e-07
TNF [NCBI] 6.24547e-08



OMIM


 OMIM Link Information
gain		 01
twinning, dizygotic [NCBI] 0.00320685
SLI2 [NCBI] 0.00199521
SLI1 [NCBI] 0.00199521
HFM [NCBI] 0.00183192
iris pattern [NCBI] 0.000995284
exstrophy of bladder [NCBI] 0.000995284
clubbing of digits [NCBI] 0.000995284
anencephaly [NCBI] 0.000971013
intelligence quantitative trait locus 1 [NCBI] 0.000731111
symphalangism, distal [NCBI] 0.000731111
mutagen sensitivity [NCBI] 0.00063205
stature quantitative trait locus 2 [NCBI] 0.00063205
antipyrine metabolism [NCBI] 0.000568085
DYX6 [NCBI] 0.000568085
otitis media, susceptibility to [NCBI] 0.000568085
achalasia, familial esophageal [NCBI] 0.00045232
beta-aminoisobutyric acid, urinary excretion of [NCBI] 0.00045232
acetabular dysplasia [NCBI] 0.00045232
strabismus, susceptibility to [NCBI] 0.00042594
neuroticism [NCBI] 0.00042594
short rib-polydactyly syndrome, type iv [NCBI] 0.000403007
AFP [NCBI] 0.000387271
BULN1 [NCBI] 0.000382751
WM1 [NCBI] 0.000382751
autism [NCBI] 0.000366197
MCKD1 [NCBI] 0.000333344
MYP2 [NCBI] 0.000319658
PAND1 [NCBI] 0.000307026
longevity [NCBI] 0.00023062
atrioventricular conduction time [NCBI] 0.000203604
PCD [NCBI] 0.00018681
TFPI2 [NCBI] 0.000165301
MAFD2 [NCBI] 0.000162091
aryl hydrocarbon hydroxylase inducibility [NCBI] 0.000159084
urogenital adysplasia, hereditary [NCBI] 0.000157673
RA [NCBI] 0.000153985
PCOS1 [NCBI] 0.000153406
TD1 [NCBI] 0.000150061
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000145296
toes, relative length of first and second [NCBI] 0.000129456
sc(1) trait of saliva [NCBI] 0.000129456
twinning due to superfetation [NCBI] 0.000129456
spastic paraplegia, optic atrophy, microcephaly, and xy sex reversal [NCBI] 0.000129456
palmomental reflex [NCBI] 0.000129456
dysphasia, familial developmental [NCBI] 0.000129456
hydrocephalus with associated malformations [NCBI] 0.000129456
proteolytic capacity of plasma [NCBI] 0.000129456
vitamin d-dependent rickets, type ii [NCBI] 0.000105391
pyridoxamine 5-prime-phosphate oxidase deficiency [NCBI] 0.000101713
electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon [NCBI] 0.000101713
magnesium, elevated red cell [NCBI] 0.000101713
ankyloblepharon filiforme adnatum and cleft palate [NCBI] 0.000101713
alkaline phosphatase, blood group-associated [NCBI] 0.000101713
mental retardation syndrome, mietens-weber type [NCBI] 0.000101713
bowing of legs, anterior, with dwarfism [NCBI] 0.000101713
RSTS [NCBI] 0.000100194
SLE [NCBI] 9.43218e-05
obesity [NCBI] 9.31348e-05
bile acid synthesis defect, congenital, 2 [NCBI] 9.12613e-05
androstenone, ability to smell [NCBI] 9.12613e-05
mydriatic response to pharmacologic agents [NCBI] 9.12613e-05
ALPP [NCBI] 8.72835e-05
CPI [NCBI] 8.51046e-05
EEG [NCBI] 8.44848e-05
hair whorl [NCBI] 8.44848e-05
novelty seeking personality trait [NCBI] 7.94538e-05
EHBA [NCBI] 7.54509e-05
oeis complex [NCBI] 7.54509e-05
gastroschisis [NCBI] 7.54509e-05
twinning, monozygotic [NCBI] 7.21273e-05
halothane hepatitis [NCBI] 7.21273e-05
BPP [NCBI] 6.92866e-05
BWS [NCBI] 6.61075e-05
hematopoietic stem cell kinetics, control of [NCBI] 6.46074e-05
GBD1 [NCBI] 6.46074e-05
myeloma, multiple [NCBI] 6.26318e-05
MS [NCBI] 6.18222e-05
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism [NCBI] 6.08391e-05
SHEP1 [NCBI] 5.91988e-05
BMND1 [NCBI] 5.91988e-05
MCPH1 [NCBI] 5.62863e-05
CFTD [NCBI] 5.62863e-05
infantile sialic acid storage disorder [NCBI] 5.49808e-05
coumarin resistance [NCBI] 5.49808e-05
DYX2 [NCBI] 5.37591e-05
dopamine beta-hydroxylase deficiency, congenital [NCBI] 5.37591e-05
SPCH1 [NCBI] 5.37591e-05
osteogenesis imperfecta, type iv [NCBI] 5.15286e-05
HSR [NCBI] 5.14464e-05
mucopolysaccharidosis type iiib [NCBI] 5.05049e-05
polycythemia vera [NCBI] 5.05049e-05
epidermolysis bullosa letalis [NCBI] 5.05049e-05
HSAN1 [NCBI] 4.95339e-05
pulmonary fibrosis, idiopathic [NCBI] 4.86107e-05
oca2 gene [NCBI] 4.76772e-05
osteoporosis [NCBI] 4.68908e-05
ABO [NCBI] 4.57033e-05
DYX1 [NCBI] 4.53166e-05
DMD [NCBI] 4.52304e-05
LPA [NCBI] 4.42798e-05
PI [NCBI] 4.0533e-05
campomelic dysplasia [NCBI] 3.95407e-05
kartagener syndrome [NCBI] 3.89994e-05
POAG [NCBI] 3.6985e-05
SMEI [NCBI] 3.6985e-05
RTT [NCBI] 3.44534e-05
sickle cell anemia [NCBI] 3.31533e-05
PNPO [NCBI] 3.30219e-05
AMC [NCBI] 3.27756e-05
GLS [NCBI] 3.15211e-05
VWS [NCBI] 3.13435e-05
CYP1A1 [NCBI] 3.07315e-05
ARMD1 [NCBI] 3.0344e-05
PLA2G1B [NCBI] 3.03256e-05
P2RX4 [NCBI] 3.03256e-05
hypogonadotropic hypogonadism [NCBI] 2.73912e-05
GTS [NCBI] 2.64077e-05
SEPT5 [NCBI] 2.59456e-05
SPTLC1 [NCBI] 2.59456e-05
osteogenesis imperfecta, type i [NCBI] 2.58478e-05
APOE [NCBI] 2.51591e-05
FGB [NCBI] 2.34612e-05
PGM3 [NCBI] 2.28221e-05
AMY1A [NCBI] 2.25269e-05
ORM1 [NCBI] 2.2246e-05
WT1 [NCBI] 2.17778e-05
CDLS1 [NCBI] 2.15913e-05
SCA1 [NCBI] 2.12251e-05
LDLR [NCBI] 2.06936e-05
ALPS [NCBI] 2.05195e-05
ADHD [NCBI] 2.05195e-05
DISC1 [NCBI] 2.01872e-05
SCZD [NCBI] 2.01792e-05
fructose intolerance, hereditary [NCBI] 1.98142e-05
hypercholesterolemia, autosomal dominant [NCBI] 1.96836e-05
ACH [NCBI] 1.85911e-05
MLL [NCBI] 1.72357e-05
PGM1 [NCBI] 1.64803e-05
F2 [NCBI] 1.63802e-05
GPT [NCBI] 1.54656e-05
hla-d histocompatibility type [NCBI] 1.4957e-05
SRS [NCBI] 1.45325e-05
HRG [NCBI] 1.43932e-05
DRPLA [NCBI] 1.38566e-05
ichthyosis, x-linked [NCBI] 1.37369e-05
PAEP [NCBI] 1.32063e-05
MC1R [NCBI] 1.28266e-05
fragile x mental retardation syndrome [NCBI] 1.27687e-05
NRG1 [NCBI] 1.26716e-05
HBA2 [NCBI] 1.1696e-05
FGFR1 [NCBI] 1.15701e-05
PON1 [NCBI] 1.10567e-05
GC [NCBI] 1.09819e-05
VEGF [NCBI] 8.95904e-06
HBA1 [NCBI] 7.7079e-06
AD [NCBI] 7.67723e-06
CP [NCBI] 6.84991e-06
STAR [NCBI] 6.78653e-06
VDR [NCBI] 6.61465e-06
WAS [NCBI] 5.7438e-06
PD [NCBI] 4.54303e-06
EGF [NCBI] 4.39539e-06
polycystic kidneys [NCBI] 3.79424e-06
HD [NCBI] 3.57155e-06
COMT [NCBI] 3.28855e-06
TTR [NCBI] 2.83391e-06
TF [NCBI] 2.68165e-06
HBB [NCBI] 2.31502e-06
EPO [NCBI] 1.07812e-06
G6PD [NCBI] 1.06048e-06
ACHE [NCBI] 5.41452e-07
CD [NCBI] 2.03952e-07
CAT [NCBI] 1.52918e-07
LPL [NCBI] 1.06204e-07
CEACAM5 [NCBI] 8.93113e-08
BDNF [NCBI] 8.17996e-08
AR [NCBI] 1.20959e-08
MDD [NCBI] 9.65638e-09



Database Center for Life Science