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MeSH keywords -> Related genes, diseases (OMIM)


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01 Spherocytosis, Hereditary [NCBI]


Gene


Gene Link Information
Gain
01
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


OMIM Link Information
gain
01
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




Database Center for Life Science