MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Uvea
[NCBI]
Gene
Gene
Link
Information
Gain
01
MS
[NCBI]
8.69867e-05
NPY
[NCBI]
1.30801e-05
TYRP1
[NCBI]
1.12596e-05
MYOC
[NCBI]
1.10333e-05
DCT
[NCBI]
1.0195e-05
FOXL2
[NCBI]
6.39673e-06
KITLG
[NCBI]
5.74432e-06
TYR
[NCBI]
5.61002e-06
LY96
[NCBI]
5.23838e-06
SOX2
[NCBI]
5.1891e-06
ATXN1
[NCBI]
4.96274e-06
KIT
[NCBI]
4.87881e-06
NOD2
[NCBI]
4.54803e-06
SERPINF1
[NCBI]
4.28081e-06
MMP2
[NCBI]
4.15907e-06
CIITA
[NCBI]
4.10685e-06
MMP9
[NCBI]
4.02907e-06
IRF1
[NCBI]
4.01212e-06
IFNGR1
[NCBI]
3.69657e-06
STAT1
[NCBI]
2.96976e-06
TLR4
[NCBI]
2.84886e-06
CCK
[NCBI]
2.19748e-06
ACHE
[NCBI]
2.03704e-06
TH
[NCBI]
1.95318e-06
TNF
[NCBI]
1.13108e-06
OMIM
OMIM
Link
Information
gain
01
MACOM
[NCBI]
0.00145218
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth
[NCBI]
0.0012742
marden-walker syndrome
[NCBI]
0.00112909
dubowitz syndrome
[NCBI]
0.00105678
coloboma, uveal, with cleft lip and palate and mental retardation
[NCBI]
0.000536184
oculopalatoskeletal syndrome
[NCBI]
0.00020079
TCOF
[NCBI]
0.000130041
BPES
[NCBI]
0.000125737
CHS
[NCBI]
9.0478e-05
NPY
[NCBI]
5.97911e-05
PTGS2
[NCBI]
3.17771e-05
TLR4
[NCBI]
1.93852e-05
VEGF
[NCBI]
1.15697e-05
CCK
[NCBI]
7.24818e-06
ACHE
[NCBI]
6.26354e-06
TH
[NCBI]
5.70598e-06
TNF
[NCBI]
1.67385e-06
Database Center for Life Science