Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Hemoglobins, Abnormal	[NCBI]

Gene	Link	Information Gain
HBB@	[NCBI]	0.00075655
HBA1	[NCBI]	0.000488201
HBAP1	[NCBI]	0.000326368
HBA@	[NCBI]	0.000326368
HBB	[NCBI]	0.000218969
HBA2	[NCBI]	0.000180064
HBG2	[NCBI]	9.76214e-05
HBG1	[NCBI]	7.60312e-05
HBD	[NCBI]	7.10143e-05
HBE1	[NCBI]	7.57875e-06
G6PD	[NCBI]	6.97519e-06
HBZ	[NCBI]	5.042e-06
ERAF	[NCBI]	2.9147e-06
MB	[NCBI]	1.41117e-06
CD1B	[NCBI]	1.25256e-06
CD1A	[NCBI]	1.18062e-06
CD1C	[NCBI]	1.1195e-06
GYPA	[NCBI]	1.05881e-06
HFE	[NCBI]	9.69198e-07
LILRB1	[NCBI]	8.98703e-07
EPB41L1	[NCBI]	5.69613e-07
EPB41L2	[NCBI]	5.48048e-07
LDLR	[NCBI]	5.36069e-07
FABP7	[NCBI]	5.23325e-07
PON1	[NCBI]	4.70683e-07
ALB	[NCBI]	4.57251e-07
TTR	[NCBI]	4.31934e-07
ADA	[NCBI]	3.13203e-07
JAK2	[NCBI]	2.75133e-07
VWF	[NCBI]	1.19665e-07
TNF	[NCBI]	7.87358e-09

OMIM	Link	Information gain
HBB	[NCBI]	0.0179651
HBA1	[NCBI]	0.00735003
HBA2	[NCBI]	0.00262402
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain	[NCBI]	0.00164597
HBG2	[NCBI]	0.00109356
HBD	[NCBI]	0.00104832
HBG1	[NCBI]	0.000758207
heinz body anemias	[NCBI]	0.000531817
HBFQTL1	[NCBI]	0.000445954
erythrocytosis, familial, 1	[NCBI]	0.000371874
TNF	[NCBI]	0.000246185
HBZ	[NCBI]	0.000160066
fibrosclerosis, multifocal	[NCBI]	0.000144836
ATMDS	[NCBI]	0.000132922
alpha-thalassemia/mental retardation syndrome, deletion-type	[NCBI]	0.000102425
erythrocytosis, familial, 2	[NCBI]	9.61957e-05
MADA	[NCBI]	9.28313e-05
pituitary dwarfism iii	[NCBI]	8.85737e-05
CLN3	[NCBI]	7.26276e-05
sickle cell anemia	[NCBI]	6.8074e-05
WRN	[NCBI]	5.86253e-05
polycystic kidneys	[NCBI]	2.97937e-05
HBE1	[NCBI]	2.9225e-05
hemoglobin--alpha locus 3	[NCBI]	1.69937e-05
ADA	[NCBI]	1.69369e-05
SLC4A1	[NCBI]	1.00694e-05
TTR	[NCBI]	7.44725e-06
AK1	[NCBI]	5.21282e-06
ATRX	[NCBI]	4.75196e-06
ALB	[NCBI]	4.46685e-06
LDLR	[NCBI]	5.99175e-07
G6PD	[NCBI]	4.79105e-07
MB	[NCBI]	2.06257e-07
HFE	[NCBI]	6.69209e-08