Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Hemoglobinopathies [NCBI]

Gene


 Gene Link Information
Gain		 01
HBB@ [NCBI] 0.00104319
HPFH [NCBI] 0.000320423
FCP1 [NCBI] 0.000282619
HBA1 [NCBI] 0.000196248
HBG1 [NCBI] 0.000180623
HBB [NCBI] 0.00017572
HBG2 [NCBI] 8.72085e-05
HBA2 [NCBI] 8.22782e-05
HBD [NCBI] 7.12585e-05
G6PD [NCBI] 4.83774e-05
BCL11A [NCBI] 3.24522e-05
GATA1 [NCBI] 2.02007e-05
HBE1 [NCBI] 1.75898e-05
OR52A1 [NCBI] 1.57264e-05
SLC4A1 [NCBI] 1.52574e-05
EPB41L1 [NCBI] 1.37777e-05
EPB41L2 [NCBI] 1.34237e-05
ANKRD49 [NCBI] 1.33461e-05
NR2C1 [NCBI] 1.33461e-05
GYPC [NCBI] 1.18645e-05
NR2C2 [NCBI] 1.10852e-05
ZFPM1 [NCBI] 9.09768e-06
CUX1 [NCBI] 8.52105e-06
EPO [NCBI] 8.27353e-06
ICAM3 [NCBI] 6.21547e-06
EPOR [NCBI] 5.73387e-06
PDE5A [NCBI] 4.13839e-06
HP [NCBI] 3.95507e-06
VHL [NCBI] 2.87337e-06
ADA [NCBI] 2.62905e-06
JAK2 [NCBI] 2.54041e-06
HFE [NCBI] 1.96967e-06
MTHFR [NCBI] 1.91332e-06



OMIM


 OMIM Link Information
gain		 01
HBFQTL2 [NCBI] 0.00498749
HBB [NCBI] 0.00300586
HBFQTL4 [NCBI] 0.0022583
HBFQTL1 [NCBI] 0.00171529
HBA1 [NCBI] 0.000890207
HBFQTL3 [NCBI] 0.000764597
HBG1 [NCBI] 0.000684723
CDAN2 [NCBI] 0.000488197
HBA2 [NCBI] 0.000393019
HBD [NCBI] 0.000363345
HBG2 [NCBI] 0.000361269
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain [NCBI] 0.000300603
erythrocytosis, familial, 1 [NCBI] 0.00017161
G6PD [NCBI] 0.000123193
ATMDS [NCBI] 0.000103324
HBZ [NCBI] 8.29598e-05
alpha-thalassemia/mental retardation syndrome, deletion-type [NCBI] 7.36928e-05
kartagener syndrome [NCBI] 5.46837e-05
HBE1 [NCBI] 4.68011e-05
HBQ1 [NCBI] 4.68011e-05
GATA1 [NCBI] 2.84504e-05
ATRX [NCBI] 2.30162e-05
PCI [NCBI] 2.12584e-05
EPOR [NCBI] 1.54604e-05
HP [NCBI] 5.0181e-06
CF [NCBI] 2.53484e-06
EPO [NCBI] 1.45597e-06
ADA [NCBI] 2.91493e-07



Database Center for Life Science