Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Anophthalmos	[NCBI]

Gene	Link	Information Gain
ANOP1	[NCBI]	0.000438875
SOX2OT	[NCBI]	0.000438875
SOX2	[NCBI]	0.000216158
SIX6	[NCBI]	7.41087e-05
OTX2	[NCBI]	5.04691e-05
RAX	[NCBI]	2.84893e-05
VSX2	[NCBI]	2.60817e-05
PAX6	[NCBI]	2.26417e-05
HESX1	[NCBI]	2.07242e-05
SIX4	[NCBI]	1.38329e-05
STRA6	[NCBI]	1.28157e-05
BCOR	[NCBI]	1.13583e-05
JMJD6	[NCBI]	1.10589e-05
SOX3	[NCBI]	9.52821e-06
SIX3	[NCBI]	9.3169e-06
FGF10	[NCBI]	8.84252e-06
GLI2	[NCBI]	8.69814e-06
HES1	[NCBI]	8.04466e-06
POU1F1	[NCBI]	7.05308e-06
BMP4	[NCBI]	6.1008e-06
BMP7	[NCBI]	5.73189e-06
NPY	[NCBI]	2.88595e-06

OMIM	Link	Information gain
MCOPS6	[NCBI]	0.0044731
microphthalmia with limb anomalies	[NCBI]	0.0044731
MCOPS3	[NCBI]	0.00127018
MCOP1	[NCBI]	0.00123297
MCOPS1	[NCBI]	0.00119995
short stature, mental retardation, callosal agenesis, heminasal hypoplasia, microphthalmia, and atypical clefting	[NCBI]	0.00100366
cerebrooculonasal syndrome	[NCBI]	0.000785962
MCOPS4	[NCBI]	0.000650784
SOX2	[NCBI]	0.000610385
fryns microphthalmia syndrome	[NCBI]	0.000518472
SIX6	[NCBI]	0.00035559
oculocerebrocutaneous syndrome	[NCBI]	0.000278692
AN2	[NCBI]	0.000203331
coloboma, ocular	[NCBI]	0.00017708
MCOPS9	[NCBI]	0.000173657
MCOPS2	[NCBI]	0.000165145
PAX6	[NCBI]	0.000148073
fraser syndrome	[NCBI]	0.000137042
sclerocornea, autosomal dominant	[NCBI]	0.000128816
CC	[NCBI]	0.000106349
dextrocardia with unusual facies and microphthalmia	[NCBI]	0.000106349
MCOP3	[NCBI]	9.78725e-05
MCOPS5	[NCBI]	9.78725e-05
moved to 310600	[NCBI]	9.78725e-05
MCOP2	[NCBI]	8.82795e-05
RAX	[NCBI]	8.81249e-05
sulfocysteinuria	[NCBI]	8.23123e-05
OTX2	[NCBI]	6.91455e-05
STRA6	[NCBI]	6.91455e-05
BCOR	[NCBI]	6.5769e-05
MAF	[NCBI]	6.12584e-05
CHX10	[NCBI]	6.12584e-05
SIX1	[NCBI]	5.81716e-05
LCA1	[NCBI]	5.73722e-05
MCOPS7	[NCBI]	5.63538e-05
walker-warburg syndrome	[NCBI]	5.28315e-05
FDH	[NCBI]	5.13272e-05
MITF	[NCBI]	3.47944e-05
NPY	[NCBI]	7.24634e-06