Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Iris Diseases	[NCBI]

Gene	Link	Information Gain
CHED1	[NCBI]	0.000415947
PITX2	[NCBI]	2.4684e-05
GPR143	[NCBI]	2.42373e-05
TYRP1	[NCBI]	2.01213e-05
PAX6	[NCBI]	1.74197e-05
RAB38	[NCBI]	1.378e-05
C1QTNF5	[NCBI]	1.33737e-05
COL8A2	[NCBI]	1.277e-05
SLC4A11	[NCBI]	1.25327e-05
PITX1	[NCBI]	1.01952e-05
PITX3	[NCBI]	9.98211e-06
ZBTB16	[NCBI]	9.68406e-06
TYR	[NCBI]	9.04228e-06
MITF	[NCBI]	8.11597e-06
NKX2-1	[NCBI]	7.13349e-06
KRT7	[NCBI]	7.02375e-06
VEGFA	[NCBI]	3.89405e-06

OMIM	Link	Information gain
iris pigment epithelium anomalies	[NCBI]	0.0032967
glaucoma-related pigment dispersion syndrome	[NCBI]	0.00123297
ataxia, spastic, with congenital miosis	[NCBI]	0.00108068
ectopia lentis with ectopia of pupil	[NCBI]	0.00072749
aniridia, cerebellar ataxia, and mental deficiency	[NCBI]	0.000588308
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging	[NCBI]	0.00051629
IRID2	[NCBI]	0.000326214
short syndrome	[NCBI]	0.000216043
RIEG1	[NCBI]	0.000172213
ophthalmoplegia, familial total, with iris transillumination	[NCBI]	0.000143802
PITX2	[NCBI]	0.000127597
PPCD3	[NCBI]	0.000121332
heterochromia iridis	[NCBI]	0.000112852
albinism, ocular, with sensorineural deafness	[NCBI]	0.000112852
coloboma, ocular	[NCBI]	9.11242e-05
WS2A	[NCBI]	8.54328e-05
PPCD1	[NCBI]	8.12332e-05
TCF8	[NCBI]	7.57683e-05
COL18A1	[NCBI]	6.3916e-05
ZNF145	[NCBI]	5.42264e-05
WT1	[NCBI]	5.35619e-05
contractural arachnodactyly, congenital	[NCBI]	5.2444e-05
SMS	[NCBI]	5.23011e-05
TYR	[NCBI]	4.63469e-05
MITF	[NCBI]	4.4726e-05
NF1	[NCBI]	3.08316e-05
VRNI	[NCBI]	2.02496e-05