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MeSH keywords -> Related genes, diseases (OMIM)


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01 Anemia, Hemolytic [NCBI]


Gene


Gene Link Information
Gain
01
DHS [NCBI] 0.000921203
G6PD [NCBI] 0.000596264
SLEH1 [NCBI] 0.000381162
NT5C3P1 [NCBI] 0.000381162
HBAP1 [NCBI] 0.000282619
ADAMTS13 [NCBI] 0.000129242
PKLR [NCBI] 7.9535e-05
NT5C3 [NCBI] 7.01938e-05
EPB41L2 [NCBI] 6.91748e-05
GPI [NCBI] 6.8809e-05
EPB41L1 [NCBI] 6.12505e-05
STOM [NCBI] 6.03651e-05
EPO [NCBI] 5.73971e-05
PGK1 [NCBI] 4.4984e-05
HBB [NCBI] 4.40576e-05
HBA2 [NCBI] 3.86323e-05
SLC4A1 [NCBI] 3.78643e-05
VWF [NCBI] 3.71949e-05
RHAG [NCBI] 3.31178e-05
EPB42 [NCBI] 3.01492e-05
ADA [NCBI] 2.96741e-05
GCLC [NCBI] 2.6686e-05
HBA1 [NCBI] 2.5619e-05
SPTA1 [NCBI] 2.31803e-05
AK1 [NCBI] 1.88488e-05
XKR3 [NCBI] 1.40605e-05
XKRX [NCBI] 1.40605e-05
CD47 [NCBI] 1.3216e-05
UCK1 [NCBI] 1.16804e-05
PIPOX [NCBI] 1.07824e-05
LCAT [NCBI] 1.03167e-05
PIGA [NCBI] 9.63713e-06
PGD [NCBI] 9.42071e-06
GYPB [NCBI] 8.88798e-06
HBZ [NCBI] 8.67325e-06
PGP [NCBI] 8.67325e-06
SMARCA5 [NCBI] 8.48253e-06
ICAM4 [NCBI] 8.31101e-06
ALDOA [NCBI] 8.15516e-06
GSS [NCBI] 8.15516e-06
H6PD [NCBI] 8.15516e-06
HK1 [NCBI] 7.75834e-06
UGT1A1 [NCBI] 7.436e-06
SPTB [NCBI] 7.00749e-06
TPI1 [NCBI] 6.93328e-06
PRDX2 [NCBI] 6.72837e-06
XK [NCBI] 6.60437e-06
KCNN4 [NCBI] 6.38073e-06
CD55 [NCBI] 6.13737e-06
SLC25A13 [NCBI] 5.8468e-06
HBG2 [NCBI] 5.50346e-06
CD59 [NCBI] 5.47271e-06
ATP7B [NCBI] 4.3014e-06
NPPA [NCBI] 4.20017e-06
CD52 [NCBI] 3.58113e-06
CXCL10 [NCBI] 3.2884e-06
TFRC [NCBI] 3.19712e-06
BPI [NCBI] 3.17513e-06
ACHE [NCBI] 3.10349e-06
CD46 [NCBI] 2.80338e-06
CTSG [NCBI] 2.6995e-06
TFPI [NCBI] 2.2132e-06
SLC2A1 [NCBI] 2.08533e-06
TROVE2 [NCBI] 1.80614e-06
FASLG [NCBI] 1.62445e-06
FOXP3 [NCBI] 1.57822e-06
HFE [NCBI] 6.7925e-07
AVP [NCBI] 6.40762e-07
CD68 [NCBI] 5.65996e-07
HIF1A [NCBI] 4.2084e-07
MPO [NCBI] 1.37099e-07
VEGFA [NCBI] 1.08156e-07




OMIM


OMIM Link Information
gain
01
stomatocytosis i [NCBI] 0.00507112
DHS [NCBI] 0.00402523
G6PD [NCBI] 0.00247346
red cell phospholipid defect with hemolysis [NCBI] 0.0022037
HBB [NCBI] 0.00176415
pyruvate kinase deficiency of red cells [NCBI] 0.00111528
6-@phosphogluconolactonase deficiency [NCBI] 0.000975838
SLEH1 [NCBI] 0.000975838
TTP [NCBI] 0.000668735
hyperbilirubinemia, rotor type [NCBI] 0.000583695
aHUS [NCBI] 0.000538359
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to [NCBI] 0.000366657
thrombocytopenic purpura, autoimmune [NCBI] 0.0003621
HS [NCBI] 0.000352279
gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to [NCBI] 0.000339298
adenosine deaminase, elevated, hemolytic anemia due to [NCBI] 0.000326926
PKLR [NCBI] 0.000324215
HBFQTL2 [NCBI] 0.000323134
PGK1 [NCBI] 0.000308792
NT5C3 [NCBI] 0.00027229
RHN [NCBI] 0.000257868
RA [NCBI] 0.000250518
EPB42 [NCBI] 0.00022334
GPI [NCBI] 0.000215465
heinz body anemias [NCBI] 0.000208132
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain [NCBI] 0.000208089
AK1 [NCBI] 0.000196975
phosphoglycerate kinase 1 deficiency [NCBI] 0.000194735
RHCE [NCBI] 0.000189661
IPEX [NCBI] 0.000173222
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to [NCBI] 0.000153661
anemia, autoimmune hemolytic [NCBI] 0.000146327
Ii [NCBI] 0.000135363
hexokinase deficiency hemolytic anemia [NCBI] 0.000127224
CF [NCBI] 0.000120234
SPTA1 [NCBI] 0.000107307
SLC4A1 [NCBI] 0.000106621
VEGF [NCBI] 0.000106504
diphosphoglycerate mutase deficiency of erythrocyte [NCBI] 0.000106476
anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [NCBI] 0.00010401
anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane [NCBI] 0.00010401
hemolytic poikilocytic anemia due to reduced ankyrin binding sites [NCBI] 0.00010401
spastic paraplegia and evans syndrome [NCBI] 0.00010401
ovalocytosis, hereditary hemolytic, with defective erythropoiesis [NCBI] 0.00010401
EL1 [NCBI] 0.000100014
hemangioma-thrombocytopenia syndrome [NCBI] 9.57602e-05
HBA2 [NCBI] 9.35504e-05
EPB72 [NCBI] 9.20435e-05
GSR [NCBI] 8.79075e-05
EPO [NCBI] 8.69008e-05
glycogen storage disease vii [NCBI] 8.56675e-05
acetophenetidin sensitivity [NCBI] 8.15639e-05
ataxic diplegia with defective cellular immunity [NCBI] 8.15639e-05
SLE [NCBI] 7.977e-05
ovalocytosis, hereditary hemolytic [NCBI] 7.31081e-05
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema [NCBI] 6.76263e-05
spherocytosis, autosomal recessive [NCBI] 6.35567e-05
gastritis, familial giant hypertrophic [NCBI] 6.35567e-05
pernicious anemia [NCBI] 6.35567e-05
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly [NCBI] 6.35567e-05
XKRX [NCBI] 6.27014e-05
RHAG [NCBI] 6.27014e-05
XKR3 [NCBI] 6.27014e-05
TPI1 [NCBI] 6.21919e-05
CD47 [NCBI] 6.01313e-05
ADAMTS13 [NCBI] 6.01313e-05
SPTB [NCBI] 5.91785e-05
ADA [NCBI] 5.39206e-05
elliptocytosis, rhesus-unlinked type [NCBI] 5.33286e-05
glutathione synthetase deficiency [NCBI] 5.15501e-05
PTPNS1 [NCBI] 4.89388e-05
SPTAN1 [NCBI] 4.89388e-05
GCLC [NCBI] 4.89388e-05
wilson disease [NCBI] 4.86516e-05
HBA1 [NCBI] 4.77845e-05
sitosterolemia [NCBI] 4.37682e-05
ANK3 [NCBI] 4.37554e-05
gilbert syndrome [NCBI] 3.86212e-05
CYP1A2 [NCBI] 3.79021e-05
PRDX2 [NCBI] 3.79021e-05
PGP [NCBI] 3.59185e-05
PRDX1 [NCBI] 3.59185e-05
PGD [NCBI] 3.59185e-05
cerebrotendinous xanthomatosis [NCBI] 3.319e-05
GSS [NCBI] 3.28652e-05
megaloblastic anemia 1 [NCBI] 3.22132e-05
PNKD1 [NCBI] 3.22132e-05
RHD [NCBI] 3.16375e-05
ADD1 [NCBI] 3.05488e-05
HK1 [NCBI] 3.05488e-05
GSTP1 [NCBI] 2.57881e-05
GPX1 [NCBI] 2.57881e-05
HBG2 [NCBI] 2.4083e-05
ACADS [NCBI] 2.1795e-05
MPO [NCBI] 1.72118e-05
ALPS [NCBI] 1.50562e-05
FOXP3 [NCBI] 1.50443e-05
protoporphyria, erythropoietic [NCBI] 1.4502e-05
porphyria cutanea tarda [NCBI] 1.30638e-05
AVP [NCBI] 1.03682e-05
CHS [NCBI] 7.16274e-06
CAT [NCBI] 3.57709e-06
hla-d histocompatibility type [NCBI] 3.32891e-06
AT [NCBI] 2.52998e-06
F3 [NCBI] 2.3837e-06
CVID [NCBI] 2.24764e-06
SOD2 [NCBI] 6.17379e-07
lymphoma, non-hodgkin, familial [NCBI] 6.01019e-07
TFPI [NCBI] 4.38635e-07
ACHE [NCBI] 2.75799e-07




Database Center for Life Science