Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Erythroblastosis, Fetal	[NCBI]

Gene	Link	Information Gain
RHCE	[NCBI]	6.64389e-05
EPO	[NCBI]	4.39963e-05
RHD	[NCBI]	3.76434e-05
SLC14A1	[NCBI]	3.22518e-05
G6PD	[NCBI]	1.90697e-05
KEL	[NCBI]	1.53531e-05
ANG	[NCBI]	9.62107e-06
DARC	[NCBI]	8.89187e-06
TFPI2	[NCBI]	7.99028e-06
SRY	[NCBI]	6.96815e-06
UGT1A1	[NCBI]	6.13685e-06
ACHE	[NCBI]	3.79689e-06
AVP	[NCBI]	3.76138e-06
VEGFA	[NCBI]	2.74257e-06
PTH	[NCBI]	2.0038e-06

OMIM	Link	Information gain
skin creases, multiple benign ring-shaped, of limbs	[NCBI]	0.0010375
EPO	[NCBI]	0.000159039
DI	[NCBI]	0.000157129
RD	[NCBI]	0.000157129
SC	[NCBI]	0.000134657
crigler-najjar syndrome	[NCBI]	8.90891e-05
KEL	[NCBI]	7.43456e-05
CD55	[NCBI]	6.91455e-05
thrombasthenia of glanzmann and naegeli	[NCBI]	6.81454e-05
G6PD	[NCBI]	6.41078e-05
RHD	[NCBI]	5.69272e-05
FY	[NCBI]	4.68337e-05
polycystic kidneys	[NCBI]	4.48257e-05
TFPI2	[NCBI]	4.42512e-05
HBD	[NCBI]	4.2474e-05
HBB	[NCBI]	1.52741e-05
ACHE	[NCBI]	8.78161e-06
AVP	[NCBI]	6.37111e-06
PTH	[NCBI]	1.45757e-06
VEGF	[NCBI]	5.93696e-08