MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Eyelid Diseases
[NCBI]
Gene
Gene
Link
Information
Gain
01
MROS
[NCBI]
0.000355204
VCF
[NCBI]
0.000340315
FOXL2
[NCBI]
6.3493e-05
FOXC2
[NCBI]
2.10198e-05
TGFBI
[NCBI]
1.65281e-05
MRPS22
[NCBI]
1.43757e-05
COL5A2
[NCBI]
1.21848e-05
COL5A1
[NCBI]
1.14212e-05
LCN1
[NCBI]
1.13353e-05
LTF
[NCBI]
9.68933e-06
CCL3
[NCBI]
8.73229e-06
MMP12
[NCBI]
8.44612e-06
COL2A1
[NCBI]
7.85035e-06
DSG3
[NCBI]
7.20338e-06
CCL5
[NCBI]
7.0127e-06
GJB2
[NCBI]
5.43194e-06
TRH
[NCBI]
4.65946e-06
GFAP
[NCBI]
3.40081e-06
EGFR
[NCBI]
2.43342e-06
EGF
[NCBI]
2.31835e-06
OMIM
OMIM
Link
Information
gain
01
schopf-schulz-passarge syndrome
[NCBI]
0.00160037
melkersson-rosenthal syndrome
[NCBI]
0.00074746
blepharocheilodontic syndrome
[NCBI]
0.000667246
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth
[NCBI]
0.000647644
sjogren syndrome
[NCBI]
0.000564232
marden-walker syndrome
[NCBI]
0.000534964
SJS1
[NCBI]
0.000399029
BPES
[NCBI]
0.000289607
aceruloplasminemia
[NCBI]
0.000266233
lipoid proteinosis of urbach and wiethe
[NCBI]
0.00014746
levator-medial rectus synkinesis
[NCBI]
0.00012988
apraxia of eyelid opening
[NCBI]
0.00012988
OCP
[NCBI]
0.0001112
trichomegaly
[NCBI]
0.000107412
poikiloderma, hereditary sclerosing
[NCBI]
0.000107412
blepharochalasis and double lip
[NCBI]
9.89352e-05
chands
[NCBI]
9.89352e-05
MRPS22
[NCBI]
8.05705e-05
trismus-pseudocamptodactyly syndrome
[NCBI]
7.72292e-05
ankyloblepharon-ectodermal defects-cleft lip/palate
[NCBI]
7.56107e-05
WS2A
[NCBI]
7.15501e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant
[NCBI]
6.73629e-05
lymphedema-distichiasis syndrome
[NCBI]
6.40463e-05
HLA-DRA
[NCBI]
6.37462e-05
FOXC2
[NCBI]
6.06151e-05
FOXL2
[NCBI]
6.06151e-05
ICAM1
[NCBI]
5.70453e-05
CP
[NCBI]
3.58856e-05
TS
[NCBI]
1.4775e-05
GFAP
[NCBI]
1.4134e-05
RP
[NCBI]
1.15363e-05
EGFR
[NCBI]
1.02837e-05
EGF
[NCBI]
8.2913e-06
MG
[NCBI]
2.83648e-06
Database Center for Life Science