Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Sex Chromatin [NCBI]

Gene


 Gene Link Information
Gain		 01
XIST [NCBI] 0.000534934
TDFA [NCBI] 1.480622e-05
SOX1 [NCBI] 1.15853e-05
SAP30 [NCBI] 1.099611e-05
SF1 [NCBI] 1.02297e-05
DAXX [NCBI] 8.66504e-06
CBX4 [NCBI] 7.84753e-06
SRY [NCBI] 7.7277e-06
WAS [NCBI] 7.44448e-06
SHBG [NCBI] 7.343e-06
H2AFX [NCBI] 7.19286e-06
G6PD [NCBI] 6.28041e-06
FASLG [NCBI] 4.52876e-06
GFAP [NCBI] 4.42773e-06



OMIM


 OMIM Link Information
gain		 01
hyperpigmentation, familial progressive [NCBI] 0.00272106
xm system [NCBI] 0.0025037
oligosynaptic infertility [NCBI] 0.00236258
nondisjunction [NCBI] 0.000563833
anus, imperforate [NCBI] 0.000398588
mental retardation, buenos aires type [NCBI] 0.000370819
GDXY [NCBI] 0.000330724
pseudohermaphroditism, incomplete male, type i [NCBI] 0.000299451
laurence-moon syndrome [NCBI] 0.000289832
CVG/MR [NCBI] 0.000284774
hairy ears [NCBI] 0.000284774
hairy ears, y-linked [NCBI] 0.000267897
reifenstein syndrome [NCBI] 0.000264868
hermaphroditism, true [NCBI] 0.00025289
AFD1 [NCBI] 0.000212862
XIST [NCBI] 0.0002052033
SRA2 [NCBI] 0.0001704337
ED1 [NCBI] 0.0001626885
NS1 [NCBI] 0.000155246
AIS [NCBI] 0.0001174048
H2AFY [NCBI] 8.97189e-05
WAS [NCBI] 8.70793e-05
H2AFX [NCBI] 7.15174e-05
SHBG [NCBI] 6.91606e-05
anemia, sideroblastic, x-linked [NCBI] 6.38941e-05
KAL1 [NCBI] 6.03817e-05
WAS [NCBI] 5.97086e-05
PWS [NCBI] 5.53816e-05
ichthyosis, x-linked [NCBI] 5.05143e-05
CBX5 [NCBI] 4.4698e-05
G6PD [NCBI] 1.921748e-05
KLK3 [NCBI] 1.055538e-05
GFAP [NCBI] 6.81873e-06
SLE [NCBI] 4.86003e-06



Database Center for Life Science