Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Uveal Diseases	[NCBI]

Gene	Link	Information Gain
OAT	[NCBI]	8.44366e-05
MS	[NCBI]	5.28348e-05
GATM	[NCBI]	1.15599e-05
RLBP1	[NCBI]	1.05382e-05
PITX1	[NCBI]	1.03273e-05
PITX3	[NCBI]	1.01142e-05
RCVRN	[NCBI]	9.65552e-06
TIMP3	[NCBI]	9.30968e-06
NF1	[NCBI]	8.85815e-06
GFAP	[NCBI]	4.21468e-06

OMIM	Link	Information gain
VRCP	[NCBI]	0.00200072
ornithine aminotransferase deficiency	[NCBI]	0.00124652
MACOM	[NCBI]	0.000844965
CHM	[NCBI]	0.000723233
glaucoma-related pigment dispersion syndrome	[NCBI]	0.000611315
SCRA	[NCBI]	0.000205943
deafness, conductive, with stapes fixation	[NCBI]	0.000157769
iris pigment layer, cleavage of	[NCBI]	0.000133566
macular dystrophy, fenestrated sheen type	[NCBI]	0.000133566
fundus dystrophy, pseudoinflammatory, recessive form	[NCBI]	0.00010262
choroideremia with deafness and obesity	[NCBI]	9.71155e-05
VRNI	[NCBI]	9.04444e-05
PPCRA	[NCBI]	8.70536e-05
bietti crystalline corneoretinal dystrophy	[NCBI]	8.4734e-05
SFD	[NCBI]	7.40678e-05
XFS	[NCBI]	7.19808e-05
PPCD1	[NCBI]	7.10309e-05
CMTX1	[NCBI]	5.96384e-05
COL18A1	[NCBI]	5.44203e-05
TIMP3	[NCBI]	4.73293e-05
WT1	[NCBI]	4.352e-05
ZS	[NCBI]	4.0314e-05
PXE	[NCBI]	3.0197e-05
SLE	[NCBI]	1.4722e-05
RP	[NCBI]	1.44766e-05
GFAP	[NCBI]	5.1522e-06
CEACAM5	[NCBI]	1.44627e-06