Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Spherocytosis, Hereditary	[NCBI]

Gene	Link	Information Gain
SLC4A1	[NCBI]	0.000351296
EPB41L1	[NCBI]	0.000163318
EPB41L2	[NCBI]	0.000160508
ANK1	[NCBI]	0.000133317
SPTB	[NCBI]	0.000118629
SPTA1	[NCBI]	6.59073e-05
EPB42	[NCBI]	3.60788e-05
UGT1A1	[NCBI]	2.73721e-05
RHAG	[NCBI]	2.43434e-05
ADD2	[NCBI]	2.19551e-05
G6PD	[NCBI]	2.05101e-05
CD47	[NCBI]	1.7137e-05
EPB49	[NCBI]	1.17264e-05
ANXA7	[NCBI]	1.08474e-05
ADD3	[NCBI]	1.01133e-05
SLC4A3	[NCBI]	9.97015e-06
PRDX2	[NCBI]	8.6816e-06
GSR	[NCBI]	8.08702e-06
EPO	[NCBI]	4.77175e-06
HFE	[NCBI]	2.22912e-06

OMIM	Link	Information gain
HS	[NCBI]	0.0039424
stomatocytosis i	[NCBI]	0.0019604
SLC4A1	[NCBI]	0.00103889
SPTB	[NCBI]	0.000513417
spherocytosis, autosomal recessive	[NCBI]	0.000360547
EPB42	[NCBI]	0.000344866
thrombocytopenic purpura, autoimmune	[NCBI]	0.00022867
elliptocytosis, rhesus-unlinked type	[NCBI]	0.000198531
SPTA1	[NCBI]	0.000197276
HPP	[NCBI]	0.000194697
trichomegaly	[NCBI]	0.000114976
hemolytic anemia with thermal sensitivity of red cells	[NCBI]	0.000114976
tuftsin deficiency	[NCBI]	9.68989e-05
hexokinase deficiency hemolytic anemia	[NCBI]	8.47765e-05
EL1	[NCBI]	7.15696e-05
ADD3	[NCBI]	5.92642e-05
SPTAN1	[NCBI]	5.92642e-05
ADD2	[NCBI]	5.40692e-05
gaucher disease, type i	[NCBI]	5.07618e-05
ADD1	[NCBI]	4.07804e-05
HK1	[NCBI]	4.07804e-05
G6PD	[NCBI]	3.97311e-05
IGHG1	[NCBI]	3.14545e-05
GSR	[NCBI]	2.84013e-05
polycystic kidneys	[NCBI]	2.60505e-05
UGT1A1	[NCBI]	2.52244e-05
PKD1	[NCBI]	1.66199e-05
APC	[NCBI]	1.06392e-05
HBB	[NCBI]	3.24053e-06
EPO	[NCBI]	8.91157e-07