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MeSH keywords -> Related genes, diseases (OMIM)


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01 Sex Chromosome Aberrations [NCBI]

Gene


 Gene Link Information
Gain		 01
MRX26 [NCBI] 0.000886252
ANOP1 [NCBI] 0.000499975
MRX64 [NCBI] 0.000499975
DFN8 [NCBI] 0.000499975
MRX14 [NCBI] 0.000499975
ACTGP10 [NCBI] 0.000499975
XCE [NCBI] 0.000458968
SRY [NCBI] 0.0004263484
ARSC2 [NCBI] 0.00041397
AUNX1 [NCBI] 0.00041397
RPSAP14 [NCBI] 0.00041397
AIC [NCBI] 0.00039106
SPG16 [NCBI] 0.000381522
VCF [NCBI] 0.000360456
XIST [NCBI] 0.0003449522
ZFY [NCBI] 0.0002515406
FMR1 [NCBI] 0.0001157782
SHOX [NCBI] 8.32431e-05
DAZ1 [NCBI] 5.8458e-05
MYT1 [NCBI] 4.9384e-05
DCX [NCBI] 4.91794e-05
L1CAM [NCBI] 4.117012e-05
NDP [NCBI] 4.02942e-05
AR [NCBI] 3.95199e-05
AMELX [NCBI] 3.590272e-05
ABCD1 [NCBI] 3.386512e-05
GJB1 [NCBI] 3.3138e-05
USP9Y [NCBI] 3.177472e-05
ARHGAP6 [NCBI] 2.88118e-05
G6PD [NCBI] 2.553989e-05
MECP2 [NCBI] 2.465436e-05
IL1RAPL1 [NCBI] 2.352513e-05
POU3F4 [NCBI] 2.267379e-05
ZIC3 [NCBI] 2.261749e-05
CDKL5 [NCBI] 2.084332e-05
XK [NCBI] 2.081958e-05
SOX3 [NCBI] 2.02225e-05
RBMY1A1 [NCBI] 1.922394e-05
TSPY1 [NCBI] 1.862356e-05
FLNA [NCBI] 1.808197e-05
CFTR [NCBI] 1.729935e-05
BTK [NCBI] 1.697325e-05
CHM [NCBI] 1.69397e-05
DKC1 [NCBI] 1.640963e-05
PLP1 [NCBI] 1.587928e-05
COL4A5 [NCBI] 1.566015e-05
KAL1 [NCBI] 1.564348e-05
TDFA [NCBI] 1.522712e-05
ZBTB7B [NCBI] 1.363208e-05
SOX9 [NCBI] 1.333972e-05
KLHL4 [NCBI] 1.318655e-05
SLC38A5 [NCBI] 1.304898e-05
TBL1Y [NCBI] 1.281016e-05
IL1RAPL2 [NCBI] 1.275317e-05
PRKY [NCBI] 1.265699e-05
POF1B [NCBI] 1.26156e-05
AMELY [NCBI] 1.242466e-05
PCDH19 [NCBI] 1.22703e-05
PPEF1 [NCBI] 1.223237e-05
CDY2A [NCBI] 1.20541e-05
DMRT2 [NCBI] 1.194529e-05
MID2 [NCBI] 1.191028e-05
SAP30 [NCBI] 1.173316e-05
DIAPH2 [NCBI] 1.16212e-05
FTSJ1 [NCBI] 1.144984e-05
CD99 [NCBI] 1.14362e-05
RPS4X [NCBI] 1.139368e-05
AFP [NCBI] 1.130019e-05
VCX [NCBI] 1.122661e-05
CYBB [NCBI] 1.110082e-05
SOX11 [NCBI] 1.097002e-05
HOXA4 [NCBI] 1.081665e-05
SOX1 [NCBI] 1.079848e-05
CDY1 [NCBI] 1.074178e-05
ACSL4 [NCBI] 1.057733e-05
CLCA2 [NCBI] 1.049981e-05
HDAC8 [NCBI] 1.034957e-05
HOXB5 [NCBI] 1.031275e-05
ARSE [NCBI] 1.023081e-05
HOXB4 [NCBI] 9.85371e-06
GK [NCBI] 9.80359e-06
WAS [NCBI] 9.7869e-06
H2AFX [NCBI] 9.69868e-06
SYCP3 [NCBI] 9.51643e-06
NHLRC1 [NCBI] 9.23063e-06
TAZ [NCBI] 9.17099e-06
MED12 [NCBI] 9.16699e-06
VPS13A [NCBI] 9.02848e-06
TIMM8A [NCBI] 8.87969e-06
MTM1 [NCBI] 8.8131e-06
EBP [NCBI] 8.65816e-06
DMRT1 [NCBI] 8.29372e-06
GDI1 [NCBI] 8.25041e-06
GPR143 [NCBI] 8.18927e-06
OTC [NCBI] 8.17965e-06
RPS6KA3 [NCBI] 8.17426e-06
DAZL [NCBI] 8.10865e-06
LGI1 [NCBI] 7.75021e-06
FOXL2 [NCBI] 7.6147e-06
OCRL [NCBI] 7.56732e-06
NR0B1 [NCBI] 7.49779e-06
ARX [NCBI] 7.2846e-06
GNRHR [NCBI] 7.09358e-06
C1QBP [NCBI] 6.91493e-06
GPC3 [NCBI] 6.81915e-06
SOX2 [NCBI] 6.79315e-06
MYOG [NCBI] 6.77674e-06
ATP1A2 [NCBI] 6.77588e-06
CD93 [NCBI] 6.67656e-06
EDA [NCBI] 6.2752e-06
GJA1 [NCBI] 6.08889e-06
KLK3 [NCBI] 5.99226e-06
MARCKS [NCBI] 5.76757e-06
ESD [NCBI] 5.69722e-06
MTRR [NCBI] 5.33133e-06
PIGA [NCBI] 5.25054e-06
MB [NCBI] 5.17881e-06
MGP [NCBI] 5.1645e-06
GHR [NCBI] 5.11362e-06
SPN [NCBI] 5.08184e-06
AQP2 [NCBI] 4.81619e-06
PAX3 [NCBI] 4.47905e-06
CYBA [NCBI] 4.40569e-06
DMPK [NCBI] 3.79826e-06
SHH [NCBI] 3.6192e-06
F8 [NCBI] 3.3924e-06
GJB2 [NCBI] 2.455297e-06
JAK2 [NCBI] 1.778833e-06
VDR [NCBI] 1.602899e-06
MTHFR [NCBI] 1.300939e-06
CTNNB1 [NCBI] 7.41799e-07
PRL [NCBI] 2.810065e-07



OMIM


 OMIM Link Information
gain		 01
fragile x mental retardation syndrome [NCBI] 0.00693551
MRX1 [NCBI] 0.0027612
oligosynaptic infertility [NCBI] 0.00266912
AIC [NCBI] 0.00257338
GBY [NCBI] 0.00230812
GCY [NCBI] 0.00207285
MCOPS1 [NCBI] 0.001964581
OFD8 [NCBI] 0.001513327
persistent hyperplastic primary vitreous, autosomal dominant [NCBI] 0.00133075
parkinsonism, early-onset, with mental retardation [NCBI] 0.00133075
brooks-wisniewski-brown syndrome [NCBI] 0.00133075
MAFD2 [NCBI] 0.001227014
SRY [NCBI] 0.001204711
terminal osseous dysplasia and pigmentary defects [NCBI] 0.001196605
mental retardation with optic atrophy, deafness, and seizures [NCBI] 0.001150297
auditory neuropathy, x-linked, 1, with peripheral sensory neuropathy [NCBI] 0.001150297
SPG16 [NCBI] 0.001150297
MRX20 [NCBI] 0.001150297
MRX2 [NCBI] 0.001150297
x inactivation, familial skewed, 2 [NCBI] 0.001120735
MCOPS4 [NCBI] 0.001097646
persistent hyperplastic primary vitreous, autosomal recessive [NCBI] 0.001097646
bullous dystrophy, hereditary macular type [NCBI] 0.001097646
CVD1 [NCBI] 0.001097646
IP [NCBI] 0.001059722
mental health wellness 1 [NCBI] 0.00105247
DFN4 [NCBI] 0.001033783
MYP1 [NCBI] 0.001033783
TKCR [NCBI] 0.001033783
OFD9 [NCBI] 0.001027808
xx male syndrome [NCBI] 0.001019486
MRX3 [NCBI] 0.000947637
EFMR [NCBI] 0.000947637
CTPP1 [NCBI] 0.000916752
immunoglobulin m, level of [NCBI] 0.000910261
pelizaeus-merzbacher-like disease, autosomal recessive, 2 [NCBI] 0.000891199
EDMD [NCBI] 0.000861807
SCAX1 [NCBI] 0.000853823
spatial visualization, aptitude for [NCBI] 0.000849062
CGF1 [NCBI] 0.000830263
MEAX [NCBI] 0.000822934
PHP [NCBI] 0.000822934
THAS [NCBI] 0.000739229
DFN2 [NCBI] 0.000739229
SLE [NCBI] 0.000737214
hyperglycerolemia [NCBI] 0.000723025
HYPX [NCBI] 0.000712976
MCOPS7 [NCBI] 0.000675566
XIST [NCBI] 0.000584224
LISX1 [NCBI] 0.000574151
CF [NCBI] 0.000556482
ND [NCBI] 0.000506473
nondisjunction [NCBI] 0.000498654
ichthyosis, x-linked [NCBI] 0.000447494
scleroderma, familial progressive [NCBI] 0.00043003
hashimoto thyroiditis [NCBI] 0.000403222
OKS [NCBI] 0.000402556
HSAS [NCBI] 0.000395107
SHOX [NCBI] 0.000389675
SGBS1 [NCBI] 0.000379842
paine syndrome [NCBI] 0.000377496
menkes disease [NCBI] 0.000364443
PCD [NCBI] 0.000344273
h-y antigen receptor [NCBI] 0.000341217
muscular dystrophy, hemizygous lethal type [NCBI] 0.000339318
GDXY [NCBI] 0.000315948
SRA2 [NCBI] 0.000313455
CDPX1 [NCBI] 0.000308135
AHC [NCBI] 0.000270826
PMD [NCBI] 0.000265394
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal [NCBI] 0.000257258
IL1RAPL1 [NCBI] 0.0002562679
radioulnar synostosis [NCBI] 0.000252272
DKC [NCBI] 0.000248686
hermaphroditism, true [NCBI] 0.000238035
campomelic dysplasia [NCBI] 0.000235858
DAZ [NCBI] 0.0002328463
SXI1 [NCBI] 0.000231853
RS1 [NCBI] 0.0002298741
FMR1 [NCBI] 0.0002288739
HMI [NCBI] 0.0002264062
XG [NCBI] 0.0002258976
spermatogenic failure, nonobstructive, y-linked [NCBI] 0.000224553
ALD [NCBI] 0.0002203499
hydrocephalus [NCBI] 0.0002188655
HTX1 [NCBI] 0.0002174833
RP2 [NCBI] 0.0002148443
ISS [NCBI] 0.0002071793
DCX [NCBI] 0.0002069828
alopecia, congenital [NCBI] 0.000204136
neuropathy, hereditary sensory, x-linked [NCBI] 0.000204136
leukemia, acute, ?x-linked [NCBI] 0.000204136
keratosis follicularis, dwarfism, and cerebral atrophy [NCBI] 0.000204136
MRX14 [NCBI] 0.000204136
omphalocele [NCBI] 0.000204136
calvarial hyperostosis [NCBI] 0.000204136
spastic paraplegia, optic atrophy, microcephaly, and xy sex reversal [NCBI] 0.000204136
AMELX [NCBI] 0.0002026685
autism [NCBI] 0.0001946444
MTS [NCBI] 0.0001944128
CLS [NCBI] 0.0001940719
heterotopia, periventricular, x-linked dominant [NCBI] 0.0001923689
MAFD1 [NCBI] 0.0001883017
infantile spasm syndrome, x-linked [NCBI] 0.0001871672
XK [NCBI] 0.0001870828
AHDS [NCBI] 0.0001852507
HEMB [NCBI] 0.0001835588
AD [NCBI] 0.0001823343
OFD1 [NCBI] 0.0001684017
CPX [NCBI] 0.0001601186
SCZD [NCBI] 0.0001589812
CGD [NCBI] 0.0001581014
L1CAM [NCBI] 0.0001551786
pallister w syndrome [NCBI] 0.0001540197
coxoauricular syndrome [NCBI] 0.0001540197
spondyloepimetaphyseal dysplasia, x-linked [NCBI] 0.0001540197
sjogren-larsson-like ichthyosis without cns or eye involvement [NCBI] 0.0001540197
body length, mouse, human homolog [NCBI] 0.0001540197
tooth size [NCBI] 0.0001540197
MCOPCT3 [NCBI] 0.0001540197
CSF2RA [NCBI] 0.0001528443
POF1 [NCBI] 0.0001518098
JARID1D [NCBI] 0.0001480318
KAL1 [NCBI] 0.0001470147
RPS4X [NCBI] 0.0001459444
PHKA1 [NCBI] 0.0001459444
ichthyosis hystrix gravior [NCBI] 0.0001455892
DMD [NCBI] 0.0001444792
breasts and nipples, absence of [NCBI] 0.0001436155
CRC [NCBI] 0.0001403182
myotubular myopathy with abnormal genital development [NCBI] 0.000135185
MRX63 [NCBI] 0.000135185
genitopalatocardiac syndrome [NCBI] 0.000135185
pterygium syndrome, multiple, x-linked [NCBI] 0.000135185
XLP1 [NCBI] 0.0001322432
mental health wellness 2 [NCBI] 0.0001246723
pseudohermaphroditism, incomplete male, type i [NCBI] 0.0001157426
POF2A [NCBI] 0.0001139717
MRX21 [NCBI] 0.0001139717
DSS [NCBI] 0.0001107851
hypogammaglobulinemia and isolated growth hormone deficiency, x-linked [NCBI] 0.0001107593
muscle glycogenosis, x-linked [NCBI] 0.0001107593
IL2RG [NCBI] 0.0001095373
HPRT1 [NCBI] 0.0001087992
KLHL4 [NCBI] 0.0001085803
neural tube defects, x-linked [NCBI] 0.0001068042
ED1 [NCBI] 0.0001058012
CHM [NCBI] 0.0001051165
MTM1 [NCBI] 0.0001047031
SMAX1 [NCBI] 0.0001037272
LNS [NCBI] 0.0001030159
ARX [NCBI] 0.0001016607
amme complex [NCBI] 0.0001008655
IL1RAPL2 [NCBI] 0.0001003373
wildervanck syndrome [NCBI] 9.90949e-05
vacterl association with hydrocephalus [NCBI] 9.85934e-05
HYR [NCBI] 9.80725e-05
glycogen storage disease ixa [NCBI] 9.78985e-05
suppressor of variegation 3-9, drosophila, homolog of, 2 [NCBI] 9.72289e-05
MRX9 [NCBI] 9.58004e-05
PHEX [NCBI] 9.50137e-05
NR0B1 [NCBI] 9.46805e-05
NDP [NCBI] 9.44501e-05
vacterl association with hydrocephalus, x-linked [NCBI] 9.38204e-05
MEA1 [NCBI] 9.37134e-05
OA1 [NCBI] 9.31749e-05
AIS [NCBI] 9.18796e-05
FLNA [NCBI] 8.94819e-05
NYS1 [NCBI] 8.92366e-05
congenital hemidysplasia with ichthyosiform erythroderma and limb defects [NCBI] 8.65735e-05
ZFP37 [NCBI] 8.65695e-05
MRX49 [NCBI] 8.65695e-05
pseudotrisomy 13 syndrome [NCBI] 8.59112e-05
ASMTL [NCBI] 8.34611e-05
PPEF1 [NCBI] 8.34611e-05
sertoli cell-only syndrome, y-linked [NCBI] 8.22384e-05
GUCY2F [NCBI] 8.14442e-05
MRXS13 [NCBI] 8.08143e-05
G6PD [NCBI] 8.00863e-05
feingold syndrome [NCBI] 7.89546e-05
ichthyosis vulgaris [NCBI] 7.89546e-05
MIC2Y [NCBI] 7.87522e-05
HHS [NCBI] 7.83169e-05
IDH3G [NCBI] 7.82726e-05
cyclic hematopoiesis [NCBI] 7.79209e-05
RENBP [NCBI] 7.77607e-05
OPD1 [NCBI] 7.56171e-05
multiple pterygium syndrome, escobar variant [NCBI] 7.56171e-05
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 7.56171e-05
denys-drash syndrome [NCBI] 7.45872e-05
NCIE1 [NCBI] 7.45872e-05
RP [NCBI] 7.43362e-05
CXORF6 [NCBI] 7.28908e-05
properdin deficiency, x-linked [NCBI] 7.15717e-05
VCX3A [NCBI] 7.13922e-05
SUV39H1 [NCBI] 7.0983e-05
TSPY [NCBI] 7.03252e-05
CCT [NCBI] 6.88934e-05
EEC3 [NCBI] 6.83761e-05
ichthyosis congenita, harlequin fetus type [NCBI] 6.74949e-05
DIAPH2 [NCBI] 6.67085e-05
IPEX [NCBI] 6.62372e-05
SPG2 [NCBI] 6.50631e-05
AFD1 [NCBI] 6.48311e-05
NSDHL [NCBI] 6.47199e-05
GJB1 [NCBI] 6.3776e-05
CD99 [NCBI] 6.37065e-05
BFLS [NCBI] 6.36873e-05
mucopolysaccharidosis type ii [NCBI] 6.30999e-05
FANCB [NCBI] 6.30683e-05
NHS [NCBI] 6.30683e-05
CBAVD [NCBI] 6.29281e-05
MNS [NCBI] 6.25567e-05
masa syndrome [NCBI] 6.19521e-05
NHS [NCBI] 6.17881e-05
MTRR [NCBI] 6.00671e-05
FACL4 [NCBI] 5.8818e-05
MCF2 [NCBI] 5.87479e-05
deafness, conductive, with stapes fixation [NCBI] 5.87473e-05
ZIC3 [NCBI] 5.59543e-05
POU3F4 [NCBI] 5.59543e-05
TIMM8A [NCBI] 5.49715e-05
MRXHF1 [NCBI] 5.44924e-05
GDI1 [NCBI] 5.4251e-05
faciogenital dysplasia [NCBI] 5.42284e-05
LAMR1 [NCBI] 5.40263e-05
ACTA1 [NCBI] 5.31571e-05
PFC [NCBI] 5.23214e-05
OCRL [NCBI] 5.04818e-05
PPSH [NCBI] 4.92987e-05
H2AFX [NCBI] 4.90158e-05
CBP [NCBI] 4.83655e-05
hemophilia a [NCBI] 4.77864e-05
EBP [NCBI] 4.72193e-05
FPLD2 [NCBI] 4.65662e-05
FDH [NCBI] 4.64468e-05
DKC1 [NCBI] 4.49884e-05
EDA [NCBI] 4.44909e-05
GK [NCBI] 4.40975e-05
CDPX2 [NCBI] 4.31773e-05
SMA3 [NCBI] 4.30824e-05
CMTX1 [NCBI] 4.30824e-05
CHM [NCBI] 4.20142e-05
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity [NCBI] 4.17434e-05
CBX5 [NCBI] 4.147563e-05
MTM1 [NCBI] 4.10744e-05
TP73L [NCBI] 4.10107e-05
RPS6KA3 [NCBI] 4.02152e-05
CYBB [NCBI] 3.88443e-05
BTHS [NCBI] 3.88124e-05
GPC3 [NCBI] 3.87234e-05
OTC [NCBI] 3.8723e-05
IKBKG [NCBI] 3.86789e-05
RB1 [NCBI] 3.83672e-05
SOX9 [NCBI] 3.75909e-05
BMD [NCBI] 3.70294e-05
PIGA [NCBI] 3.66967e-05
AR [NCBI] 3.54342e-05
thyroid carcinoma, papillary [NCBI] 3.39606e-05
F13A1 [NCBI] 3.32199e-05
FOXP3 [NCBI] 3.00622e-05
BPES [NCBI] 2.94974e-05
bullous erythroderma ichthyosiformis congenita of brocq [NCBI] 2.89107e-05
MAOA [NCBI] 2.705214e-05
ABCD1 [NCBI] 2.70272e-05
ornithine transcarbamylase deficiency, hyperammonemia due to [NCBI] 2.67488e-05
BTK [NCBI] 2.2153e-05
PRL [NCBI] 2.196826e-05
hypogonadotropic hypogonadism [NCBI] 2.156854e-05
alopecia, androgenetic [NCBI] 1.964442e-05
RHO [NCBI] 1.957396e-05
NS1 [NCBI] 1.776233e-05
DNMT1 [NCBI] 1.761138e-05
MECP2 [NCBI] 1.687436e-05
GHR [NCBI] 1.439288e-05
fabry disease [NCBI] 1.356817e-05
WAS [NCBI] 1.336524e-05
MB [NCBI] 1.228871e-05
DMD [NCBI] 1.217261e-05
AFP [NCBI] 7.56572e-06
TYMS [NCBI] 6.94386e-06
PWS [NCBI] 3.099065e-06
PJS [NCBI] 2.66418e-06
CFTR [NCBI] 1.40489e-06
AS [NCBI] 6.475248e-07
VDR [NCBI] 1.773148e-08



Database Center for Life Science