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MeSH keywords -> Related genes, diseases (OMIM)


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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