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MeSH keywords -> Related genes, diseases (OMIM)


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01 Anemia, Hemolytic, Congenital [NCBI]

Gene


 Gene Link Information
Gain		 01
DHS [NCBI] 0.00169106
HBB@ [NCBI] 0.000175118
TEC [NCBI] 0.000175118
G6PD [NCBI] 0.000131845
STOM [NCBI] 0.000111572
HBB [NCBI] 8.42841e-05
SPTA1 [NCBI] 7.53687e-05
PKLR [NCBI] 6.52601e-05
HBA1 [NCBI] 6.21672e-05
EPB41L2 [NCBI] 6.10881e-05
EPB41L1 [NCBI] 5.17692e-05
ALDOA [NCBI] 3.50423e-05
ADA [NCBI] 3.25915e-05
NT5C3 [NCBI] 2.17856e-05
GSS [NCBI] 2.17856e-05
AK1 [NCBI] 2.17856e-05
SPTB [NCBI] 1.94037e-05
TPI1 [NCBI] 1.92512e-05
GPI [NCBI] 1.52012e-05
HBA2 [NCBI] 1.5156e-05
ADAMTS13 [NCBI] 1.51252e-05
NT5C [NCBI] 1.22467e-05
AMPD3 [NCBI] 1.16634e-05
EPB49 [NCBI] 1.12297e-05
FLOT2 [NCBI] 1.05968e-05
HFE [NCBI] 1.05884e-05
MGAT2 [NCBI] 1.01359e-05
FLOT1 [NCBI] 9.94486e-06
ADD2 [NCBI] 9.2193e-06
HK1 [NCBI] 9.2193e-06
CPOX [NCBI] 8.62573e-06
RHD [NCBI] 8.32041e-06
RHCE [NCBI] 8.0615e-06
VWF [NCBI] 7.9393e-06
PGK1 [NCBI] 7.59203e-06
HTT [NCBI] 7.35071e-06
HBG2 [NCBI] 6.95346e-06
SLC4A1 [NCBI] 6.22669e-06
MPZ [NCBI] 5.6908e-06
UGT1A1 [NCBI] 3.97534e-06



OMIM


 OMIM Link Information
gain		 01
DHS [NCBI] 0.00948734
stomatocytosis i [NCBI] 0.00779183
CDAN2 [NCBI] 0.00408452
pseudohyperkalemia, familial, 1, due to red cell leak [NCBI] 0.00341984
HBB [NCBI] 0.00121246
CDAN3 [NCBI] 0.00103862
G6PD [NCBI] 0.000913066
HPP [NCBI] 0.000877253
pyruvate kinase deficiency of red cells [NCBI] 0.000819024
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to [NCBI] 0.000790414
stomatocytosis ii [NCBI] 0.000651642
SPTA1 [NCBI] 0.000480865
anemia, dyserythropoietic congenital, type i [NCBI] 0.000424472
red cell phospholipid defect with hemolysis [NCBI] 0.00042133
GPI [NCBI] 0.000269965
hexokinase deficiency hemolytic anemia [NCBI] 0.000258231
phosphoglycerate kinase 1 deficiency [NCBI] 0.000239379
hemolytic anemia with thermal sensitivity of red cells [NCBI] 0.00023784
ALDOA [NCBI] 0.000220455
PKLR [NCBI] 0.000206993
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema [NCBI] 0.000192916
pseudohyperkalemia cardiff [NCBI] 0.000192916
spherocytosis, autosomal recessive [NCBI] 0.000183322
adenosine deaminase, elevated, hemolytic anemia due to [NCBI] 0.000164976
GSS [NCBI] 0.000153987
HBA1 [NCBI] 0.00013362
TPI1 [NCBI] 0.000124325
AK1 [NCBI] 0.000119625
XK [NCBI] 0.000119625
hemolytic anemia, congenital, with emphysema and cutis laxa [NCBI] 0.000118781
HBA2 [NCBI] 0.000117411
RA [NCBI] 0.00010903
PGK1 [NCBI] 0.000102558
majeed syndrome [NCBI] 8.23491e-05
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to [NCBI] 7.82637e-05
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly [NCBI] 7.82637e-05
anemia, microcytic [NCBI] 7.50102e-05
ADAMTS13 [NCBI] 7.21631e-05
ADA [NCBI] 6.9235e-05
elliptocytosis, rhesus-unlinked type [NCBI] 6.79721e-05
EL1 [NCBI] 5.30584e-05
TTP [NCBI] 5.03343e-05
glycogen storage disease vii [NCBI] 4.59951e-05
malaria, susceptibility to [NCBI] 4.50762e-05
EPB72 [NCBI] 4.39477e-05
Ss [NCBI] 4.19559e-05
NT5C3 [NCBI] 4.03011e-05
hypertrophic neuropathy of dejerine-sottas [NCBI] 4.01552e-05
LPIN2 [NCBI] 3.88859e-05
aHUS [NCBI] 3.77647e-05
RHCE [NCBI] 3.76499e-05
HK1 [NCBI] 3.65529e-05
MN [NCBI] 3.5567e-05
EPB42 [NCBI] 3.30966e-05
gaucher disease, type i [NCBI] 3.26663e-05
GPX1 [NCBI] 3.17424e-05
SPTB [NCBI] 2.85476e-05
FY [NCBI] 2.76829e-05
DBA [NCBI] 2.60401e-05
GSR [NCBI] 2.42561e-05
coproporphyria [NCBI] 2.29221e-05
SLC4A1 [NCBI] 1.89591e-05
HS [NCBI] 1.80474e-05
MPZ [NCBI] 1.5138e-05
LCAT [NCBI] 6.94907e-06



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