MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Hemoglobins, Abnormal
[NCBI]
Gene
Gene
Link
Information
Gain
01
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
OMIM
Link
Information
gain
01
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
Database Center for Life Science