Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Eyelid Diseases	[NCBI]

Gene	Link	Information Gain
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	Link	Information gain
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