Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Indocyanine Green	[NCBI]

Gene	Link	Information Gain
VEGFA	[NCBI]	6.45082e-06
BEST1	[NCBI]	3.89673e-06
RCVRN	[NCBI]	3.74283e-06
BAX	[NCBI]	3.47127e-06
MUC1	[NCBI]	2.93183e-06
EFEMP1	[NCBI]	2.00612e-06
SLCO1B1	[NCBI]	1.69969e-06
TIMP3	[NCBI]	1.6598e-06
ABCA4	[NCBI]	1.63942e-06
PAX2	[NCBI]	1.60423e-06
SERPINF1	[NCBI]	1.38385e-06
CLU	[NCBI]	1.33159e-06
TNF	[NCBI]	1.33065e-06
MB	[NCBI]	1.30934e-06
XRCC5	[NCBI]	1.23637e-06
VHL	[NCBI]	1.20544e-06
CD68	[NCBI]	1.03024e-06
BCL2L1	[NCBI]	9.69488e-07
AFP	[NCBI]	8.78549e-07
GFAP	[NCBI]	8.17949e-07
CCK	[NCBI]	8.02975e-07
CDKN1A	[NCBI]	7.33423e-07
CASP3	[NCBI]	6.96743e-07

OMIM	Link	Information gain
chorioretinal atrophy, progressive bifocal	[NCBI]	0.00202368
VRNI	[NCBI]	0.000323902
ARMD1	[NCBI]	0.000195375
angioid streaks	[NCBI]	0.00015942
sturge-weber syndrome	[NCBI]	0.000147501
papillorenal syndrome	[NCBI]	0.000112624
RP	[NCBI]	9.87896e-05
ehlers-danlos syndrome, type iv, autosomal dominant	[NCBI]	9.63936e-05
VMD	[NCBI]	8.83637e-05
PXE	[NCBI]	5.90855e-05
CEACAM5	[NCBI]	2.82473e-05
VEGF	[NCBI]	2.68876e-05
ABCB11	[NCBI]	2.25979e-05
NF1	[NCBI]	1.93865e-05
PEDF	[NCBI]	1.86638e-05
MB	[NCBI]	1.41206e-05
CF	[NCBI]	6.40702e-06
TNF	[NCBI]	6.10436e-06
AFP	[NCBI]	5.91258e-06
SLE	[NCBI]	5.90837e-06
GFAP	[NCBI]	4.82857e-06
CCK	[NCBI]	4.56329e-06