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01 Sex Chromosomes [NCBI]

Gene


 Gene Link Information
Gain		 01
DCE [NCBI] 0.000617201
TKCR [NCBI] 0.000617201
C1HR [NCBI] 0.000617201
NANOGP2 [NCBI] 0.000510457
ADFN [NCBI] 0.000483315
XCE [NCBI] 0.00047712
DMRT1 [NCBI] 0.0002367299
G6PD [NCBI] 0.0001347022
SRY [NCBI] 8.47131e-05
ZFY [NCBI] 7.12778e-05
SOX9 [NCBI] 3.25739e-05
SHOX [NCBI] 3.18051e-05
MPI [NCBI] 2.925465e-05
ZFX [NCBI] 2.030037e-05
RPS4Y1 [NCBI] 1.932492e-05
UTY [NCBI] 1.91453e-05
PCDH11X [NCBI] 1.894209e-05
JARID1D [NCBI] 1.800892e-05
JARID1C [NCBI] 1.793607e-05
SYCP3 [NCBI] 1.728208e-05
STS [NCBI] 1.685775e-05
AMELX [NCBI] 1.639673e-05
USP9Y [NCBI] 1.576964e-05
NR0B1 [NCBI] 1.4933e-05
WNT4 [NCBI] 1.217967e-05
APRT [NCBI] 1.169804e-05
CD99 [NCBI] 1.150938e-05
ESD [NCBI] 1.144832e-05
DHRSX [NCBI] 1.136709e-05
TDFA [NCBI] 1.120439e-05
AMH [NCBI] 1.117233e-05
GTPBP6 [NCBI] 1.093484e-05
SYCE2 [NCBI] 1.050307e-05
ASMTL [NCBI] 1.025403e-05
SFRS17A [NCBI] 9.95555e-06
PPP2R3B [NCBI] 9.85022e-06
EIF1AY [NCBI] 9.85022e-06
TBL1Y [NCBI] 9.59619e-06
SMS [NCBI] 9.44297e-06
SUV39H2 [NCBI] 9.29609e-06
H2AFX [NCBI] 9.25488e-06
PCDH19 [NCBI] 9.16475e-06
CRISP2 [NCBI] 8.95907e-06
UTX [NCBI] 8.78454e-06
CTDSP1 [NCBI] 8.67372e-06
EIF2S3 [NCBI] 8.67372e-06
HINT3 [NCBI] 8.65176e-06
PQBP1 [NCBI] 8.50769e-06
PCDH11Y [NCBI] 8.50127e-06
OFD1 [NCBI] 8.33075e-06
ODF1 [NCBI] 8.17274e-06
RPS4X [NCBI] 8.15379e-06
POU3F4 [NCBI] 8.02249e-06
PHKA2 [NCBI] 7.96787e-06
SPIN1 [NCBI] 7.83021e-06
AK1 [NCBI] 7.81505e-06
LHX1 [NCBI] 7.78856e-06
DDX3Y [NCBI] 7.78856e-06
RGN [NCBI] 7.63746e-06
XK [NCBI] 7.41461e-06
PEG3 [NCBI] 7.36226e-06
FLG [NCBI] 6.94878e-06
NP [NCBI] 6.9212e-06
PGK1 [NCBI] 6.73831e-06
RHCE [NCBI] 6.68198e-06
EIF1AX [NCBI] 6.59478e-06
HEXA [NCBI] 6.57103e-06
HPRT1 [NCBI] 6.43911e-06
FGF9 [NCBI] 6.3257e-06
GATA4 [NCBI] 6.12101e-06
KAL1 [NCBI] 6.09609e-06
GNRHR [NCBI] 6.03861e-06
REN [NCBI] 5.93875e-06
PRLR [NCBI] 5.40336e-06
ABCD1 [NCBI] 5.33764e-06
TRH [NCBI] 5.28282e-06
FGFR2 [NCBI] 4.82756e-06
SYK [NCBI] 4.71777e-06
TAP2 [NCBI] 4.00872e-06
ATR [NCBI] 3.84862e-06
FMR1 [NCBI] 3.4154e-06
MSH2 [NCBI] 3.384577e-06
SPI1 [NCBI] 3.36181e-06
BTK [NCBI] 3.2587e-06
ADA [NCBI] 2.59856e-06
CFTR [NCBI] 1.108867e-06
ACHE [NCBI] 1.030331e-06
PTH [NCBI] 8.45397e-07



OMIM


 OMIM Link Information
gain		 01
MRX1 [NCBI] 0.01089098
MAFD2 [NCBI] 0.00983995
spatial visualization, aptitude for [NCBI] 0.00712382
immunoglobulin m, level of [NCBI] 0.00695809
TKCR [NCBI] 0.00482402
GCY [NCBI] 0.00339816
fragile x mental retardation syndrome [NCBI] 0.00298633
EFMR [NCBI] 0.00244426
hodgkin disease, x-linked pseudoautosomal [NCBI] 0.00242083
ST3 [NCBI] 0.00222126
unique green phenomenon [NCBI] 0.001912304
hodgkin disease, y-linked pseudoautosomal [NCBI] 0.001912304
PCD [NCBI] 0.001832796
ichthyosis, x-linked [NCBI] 0.001717924
retinoschisis of fovea [NCBI] 0.001340275
CACD [NCBI] 0.001340275
MRSD [NCBI] 0.001340275
amelogenesis imperfecta, hypoplastic type [NCBI] 0.001340275
deafness, high-frequency sensorineural, x-linked [NCBI] 0.001340275
malignant atrophic papulosis [NCBI] 0.001317954
MF4 [NCBI] 0.001225313
xm system [NCBI] 0.001126968
OPA2 [NCBI] 0.001126968
DMD [NCBI] 0.001076646
G6PD [NCBI] 0.001071353
HPRT1 [NCBI] 0.001052271
acromial dimples [NCBI] 0.0009989
arthrogryposis multiplex congenita, distal, x-linked [NCBI] 0.000989912
MYP1 [NCBI] 0.000989912
oligosynaptic infertility [NCBI] 0.000989912
h-y antigen receptor [NCBI] 0.00094833
ED1 [NCBI] 0.00090636
DA5 [NCBI] 0.000822034
gonadal dysgenesis, xx type, with deafness [NCBI] 0.000822034
SCAX1 [NCBI] 0.00080956
gordon syndrome [NCBI] 0.000796371
PHP [NCBI] 0.000779285
DYT2 [NCBI] 0.000775818
ADFN [NCBI] 0.000774154
CGD [NCBI] 0.000764555
DFN2 [NCBI] 0.000753622
LNS [NCBI] 0.000727731
gonadal dysgenesis, xy type [NCBI] 0.000711865
PGK1 [NCBI] 0.00070778
HSAS [NCBI] 0.000705943
MCOPS1 [NCBI] 0.000663053
BMD [NCBI] 0.000640632
hairy ears, y-linked [NCBI] 0.000600985
HYR [NCBI] 0.000560925
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 0.000554448
TBG [NCBI] 0.000551676
tyrosine aminotransferase, regulator of [NCBI] 0.000534163
robinow syndrome, autosomal dominant [NCBI] 0.000533557
CDPX2 [NCBI] 0.000487704
AIS [NCBI] 0.000457389
EDMD [NCBI] 0.000421166
endocardial fibroelastosis [NCBI] 0.000400453
aneurysm, intracranial berry, 1 [NCBI] 0.00039169
diabetes insipidus, nephrogenic, x-linked [NCBI] 0.000384044
MRX59 [NCBI] 0.000371992
fragile site 2q11 [NCBI] 0.000342905
CCT [NCBI] 0.000325749
XIST [NCBI] 0.000325139
CMTX1 [NCBI] 0.00032121
CD99 [NCBI] 0.000313171
xx male syndrome [NCBI] 0.000312431
fabry disease [NCBI] 0.000306756
nondisjunction [NCBI] 0.000299004
RENS1 [NCBI] 0.000296387
ichthyosis vulgaris [NCBI] 0.000283665
FMD [NCBI] 0.000273323
hemopoietic proliferation [NCBI] 0.000266979
dyggve-melchior-clausen syndrome, x-linked [NCBI] 0.000266979
fragile site 9q32 [NCBI] 0.000266979
STHAGX1 [NCBI] 0.000266979
VURX [NCBI] 0.000266979
TAQ1 [NCBI] 0.000266979
dens evaginatus [NCBI] 0.000266979
opticoacoustic nerve atrophy with dementia [NCBI] 0.000266979
CHM [NCBI] 0.000265924
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 0.000261955
JARID1D [NCBI] 0.000247469
alport syndrome, autosomal dominant [NCBI] 0.0002463768
NS1 [NCBI] 0.0002420158
AIED [NCBI] 0.000241997
von willebrand disease, x-linked form [NCBI] 0.0002392707
myoclonic epilepsy, progressive [NCBI] 0.0002392707
phosphoribosylpyrophosphate synthetase superactivity [NCBI] 0.000235789
hypogonadism, male [NCBI] 0.000227833
MNS [NCBI] 0.000227551
cyanide, inability to smell [NCBI] 0.0002221109
deafness, conductive, with stapes fixation [NCBI] 0.0002139216
taurodontism [NCBI] 0.0002131391
incisors, shovel-shaped [NCBI] 0.0002131391
MRXHF1 [NCBI] 0.0002062562
CPX [NCBI] 0.0002062562
CBD [NCBI] 0.0002051324
POF1 [NCBI] 0.000204237
spinocerebellar ataxia, x-linked 3 [NCBI] 0.0002001247
DHS [NCBI] 0.0002001247
mcdonough syndrome [NCBI] 0.0002001247
factor viii deficiency [NCBI] 0.0002001247
tooth size [NCBI] 0.0002001247
OFD7 [NCBI] 0.0002001247
testicular torsion [NCBI] 0.0002001247
radiation sensitivity of natural killer activity [NCBI] 0.0002001247
glutamyl ribose-5-phosphate storage disease [NCBI] 0.0002001247
glycogen storage disease ixa [NCBI] 0.000195303
HEMB [NCBI] 0.0001916564
AHC [NCBI] 0.0001897166
XG [NCBI] 0.0001793345
RP2 [NCBI] 0.0001750325
male infertility with large-headed, multiflagellar, polyploid spermatozoa [NCBI] 0.0001750132
mental retardation, x-linked, snyder-robinson type [NCBI] 0.0001750132
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis [NCBI] 0.0001750132
XLP1 [NCBI] 0.0001698344
larynx, congenital partial atresia of [NCBI] 0.000168271
hypophosphatemic rickets, x-linked dominant [NCBI] 0.0001662232
LWD [NCBI] 0.0001658905
von willebrand disease, recessive form [NCBI] 0.0001595937
thyroxine-binding globulin of serum [NCBI] 0.0001593057
PRD [NCBI] 0.0001587747
leigh syndrome, x-linked [NCBI] 0.0001587747
corpus callosum, partial agenesis of, x-linked [NCBI] 0.0001587747
CMM [NCBI] 0.0001546019
lenz-majewski hyperostotic dwarfism [NCBI] 0.0001517469
hurler syndrome [NCBI] 0.0001475009
CSNB1B [NCBI] 0.0001465202
ruvalcaba syndrome [NCBI] 0.0001461731
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.0001456314
BTK [NCBI] 0.0001447926
mental retardation, fra12a type [NCBI] 0.0001427816
neural tube defects, x-linked [NCBI] 0.0001372078
OA1 [NCBI] 0.0001364106
GDXY [NCBI] 0.0001343422
reifenstein syndrome [NCBI] 0.0001342405
ichthyosis, bullous type [NCBI] 0.0001339186
PHEX [NCBI] 0.0001319688
MTM1 [NCBI] 0.0001313023
MIC2Y [NCBI] 0.0001290423
bkm dna [NCBI] 0.0001290423
arbitrary restriction polymorphism 1 [NCBI] 0.0001286667
ND [NCBI] 0.0001272407
hermaphroditism, true [NCBI] 0.0001225686
TRS [NCBI] 0.0001225686
AHO [NCBI] 0.0001195484
AIH2 [NCBI] 0.0001191489
phosphoglycerate kinase 1 deficiency [NCBI] 0.0001160167
hematopoietic stem cell kinetics, control of [NCBI] 0.0001115149
diabetes insipidus, nephrogenic, autosomal [NCBI] 0.0001111753
MCOPS2 [NCBI] 0.0001087376
SEDT [NCBI] 0.0001078152
THC1 [NCBI] 0.0001051083
SRA2 [NCBI] 0.0001038745
OPD1 [NCBI] 0.0001035023
SFD [NCBI] 0.0001026601
CMT4A [NCBI] 0.0001026601
mucopolysaccharidosis type ii [NCBI] 0.0001007677
HEPH [NCBI] 0.0001001331
ENO1 [NCBI] 9.73405e-05
hemophilia a [NCBI] 9.71345e-05
MTS [NCBI] 9.3927e-05
SPG2 [NCBI] 9.35189e-05
XK [NCBI] 9.27859e-05
DCE [NCBI] 8.95775e-05
acetylserotonin methyltransferase-like, y-linked [NCBI] 8.95775e-05
AHDS [NCBI] 8.9574e-05
ESD [NCBI] 8.95183e-05
IPEX [NCBI] 8.73616e-05
TAF1 [NCBI] 8.56657e-05
CDPX1 [NCBI] 8.3727e-05
NHS [NCBI] 8.20862e-05
GLA [NCBI] 8.07918e-05
anemia, sideroblastic, x-linked [NCBI] 8.07786e-05
AVPR2 [NCBI] 8.01289e-05
OFD1 [NCBI] 7.94333e-05
OCA2 [NCBI] 7.78677e-05
NR0B1 [NCBI] 7.61635e-05
IP [NCBI] 7.55928e-05
RS1 [NCBI] 7.53315e-05
PGM1 [NCBI] 7.3711e-05
EIF2S3 [NCBI] 7.13607e-05
SYCE2 [NCBI] 7.13607e-05
MADD [NCBI] 7.12479e-05
ehlers-danlos syndrome, type i [NCBI] 7.10436e-05
CFNS [NCBI] 6.96725e-05
WFS1 [NCBI] 6.90861e-05
faciogenital dysplasia [NCBI] 6.72828e-05
FDH [NCBI] 6.4862e-05
suppressor of variegation 3-9, drosophila, homolog of, 2 [NCBI] 6.44939e-05
ASMTL [NCBI] 6.44939e-05
IHG [NCBI] 6.44939e-05
DKC [NCBI] 6.42267e-05
SGBS1 [NCBI] 6.40459e-05
APRT [NCBI] 6.39641e-05
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i [NCBI] 6.38932e-05
RBS [NCBI] 6.36242e-05
CLL [NCBI] 6.34694e-05
MCOPS7 [NCBI] 6.14684e-05
MEA1 [NCBI] 5.85423e-05
PARP2 [NCBI] 5.73503e-05
INSRR [NCBI] 5.67313e-05
AP1S2 [NCBI] 5.67313e-05
ASS [NCBI] 5.65475e-05
C1QG [NCBI] 5.636e-05
C1QB [NCBI] 5.636e-05
BCOR [NCBI] 5.55393e-05
mitochondrial complex i deficiency [NCBI] 5.5462e-05
AK2 [NCBI] 5.52898e-05
NHS [NCBI] 5.4549e-05
SRY [NCBI] 5.42168e-05
VMD [NCBI] 5.41587e-05
SMS [NCBI] 5.40978e-05
HIGM1 [NCBI] 5.40322e-05
ATS [NCBI] 5.23558e-05
ATM [NCBI] 5.1582e-05
C1QA [NCBI] 5.02742e-05
SYCP3 [NCBI] 4.77494e-05
PEPC [NCBI] 4.71593e-05
SCIDX1 [NCBI] 4.64088e-05
CMT1B [NCBI] 4.5659e-05
FGD1 [NCBI] 4.56534e-05
MDH1 [NCBI] 4.56534e-05
ZFX [NCBI] 4.56534e-05
MID1 [NCBI] 4.46272e-05
PKM2 [NCBI] 4.46272e-05
LAD [NCBI] 4.45902e-05
spermatogenic failure, nonobstructive, y-linked [NCBI] 4.45902e-05
ZFY [NCBI] 4.39802e-05
MAD2L1 [NCBI] 4.39802e-05
MPI [NCBI] 4.3528e-05
IDH1 [NCBI] 4.3388e-05
PRPS1 [NCBI] 4.29358e-05
ACO1 [NCBI] 4.25164e-05
PEPA [NCBI] 4.23899e-05
FLG [NCBI] 4.23514e-05
PDE4D [NCBI] 4.18837e-05
CBP [NCBI] 4.10901e-05
PGK2 [NCBI] 4.10733e-05
CMPK1 [NCBI] 4.0869e-05
ALDOA [NCBI] 3.95662e-05
H2AFX [NCBI] 3.87092e-05
hypogonadotropic hypogonadism [NCBI] 3.8665e-05
AMELX [NCBI] 3.73478e-05
RB1 [NCBI] 3.55963e-05
SPTB [NCBI] 3.48836e-05
LDHB [NCBI] 3.48508e-05
MTM1 [NCBI] 3.42546e-05
AVSD [NCBI] 3.40508e-05
CES [NCBI] 3.2588e-05
IGF1R [NCBI] 3.20209e-05
AK1 [NCBI] 3.20209e-05
SHOX [NCBI] 3.16768e-05
fucosidosis [NCBI] 3.03798e-05
INCENP [NCBI] 3.02329e-05
IGHG1 [NCBI] 2.99543e-05
ACP1 [NCBI] 2.96775e-05
ATRX [NCBI] 2.87304e-05
OTC [NCBI] 2.86324e-05
REN [NCBI] 2.82058e-05
AMH [NCBI] 2.79193e-05
menkes disease [NCBI] 2.77291e-05
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 2.76537e-05
PTH [NCBI] 2.73507e-05
tyrosinemia, type i [NCBI] 2.69011e-05
L1CAM [NCBI] 2.66624e-05
LHCGR [NCBI] 2.62154e-05
SH2D1A [NCBI] 2.5629e-05
NP [NCBI] 2.50742e-05
ITGB2 [NCBI] 2.46527e-05
NR5A1 [NCBI] 2.27966e-05
HEXA [NCBI] 2.208867e-05
HLA-A [NCBI] 2.176554e-05
FOXP3 [NCBI] 2.16171e-05
ACH [NCBI] 2.100501e-05
MAOA [NCBI] 2.081901e-05
ACHE [NCBI] 2.059856e-05
MPZ [NCBI] 2.040765e-05
MYOC [NCBI] 1.999339e-05
PRLR [NCBI] 1.810451e-05
GUSB [NCBI] 1.721551e-05
HFE [NCBI] 1.58204e-05
INSR [NCBI] 1.573114e-05
FA [NCBI] 1.345578e-05
PMD [NCBI] 1.224505e-05
leber optic atrophy [NCBI] 1.132603e-05
SMAX1 [NCBI] 1.038335e-05
ALD [NCBI] 9.06591e-06
NF1 [NCBI] 8.86753e-06
SOD1 [NCBI] 7.90304e-06
lymphoma, non-hodgkin, familial [NCBI] 7.221434e-06
HP [NCBI] 6.78601e-06
RTT [NCBI] 3.985527e-06
CFTR [NCBI] 3.25632e-06
HD [NCBI] 2.206098e-06
AR [NCBI] 5.213e-07
WAS [NCBI] 2.218249e-07
ADA [NCBI] 1.09520173e-07



Database Center for Life Science