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MeSH keywords -> Related genes, diseases (OMIM)


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01 Erythrocytes, Abnormal [NCBI]

Gene


 Gene Link Information
Gain		 01
DHS [NCBI] 0.00222215
EPB41L2 [NCBI] 0.000100185
EPB41L1 [NCBI] 8.80712e-05
STOM [NCBI] 6.82031e-05
SPTA1 [NCBI] 6.30646e-05
BCAM [NCBI] 3.26073e-05
SLC4A1 [NCBI] 2.68902e-05
HBA1 [NCBI] 1.78001e-05
EPB41 [NCBI] 1.70248e-05
EPO [NCBI] 1.28591e-05
GYPC [NCBI] 1.25847e-05
ICAM4 [NCBI] 1.25847e-05
SPTB [NCBI] 1.14907e-05
HBB [NCBI] 9.47831e-06
ACTB [NCBI] 8.51001e-06
EDN1 [NCBI] 8.22503e-06
GATA1 [NCBI] 6.92657e-06
SLC12A4 [NCBI] 6.15882e-06
SLC12A7 [NCBI] 5.94352e-06
FLOT2 [NCBI] 5.76649e-06
PRDM16 [NCBI] 5.61616e-06
EPB49 [NCBI] 5.48554e-06
SLC12A6 [NCBI] 5.44554e-06
FLOT1 [NCBI] 5.40708e-06
HBA2 [NCBI] 5.33434e-06
ZFPM1 [NCBI] 5.17278e-06
SLC16A1 [NCBI] 5.14339e-06
ABCG8 [NCBI] 5.06008e-06
ADA [NCBI] 5.02637e-06
ABCG5 [NCBI] 5.00817e-06
XRCC3 [NCBI] 4.91183e-06
MFGE8 [NCBI] 4.76285e-06
PRDX2 [NCBI] 4.61609e-06
EPHX1 [NCBI] 4.59918e-06
RAP1A [NCBI] 4.55011e-06
PRDX3 [NCBI] 4.50336e-06
CYP1A1 [NCBI] 4.19225e-06
RAPGEF3 [NCBI] 4.18118e-06
KCNN4 [NCBI] 4.07686e-06
KLF1 [NCBI] 4.0476e-06
GSTT1 [NCBI] 4.03803e-06
SELE [NCBI] 3.94715e-06
CD59 [NCBI] 3.87194e-06
ADAMTS13 [NCBI] 3.7581e-06
GSTM1 [NCBI] 3.68226e-06
PIGA [NCBI] 3.67564e-06
VCAM1 [NCBI] 3.61185e-06
CD47 [NCBI] 3.55778e-06
ERCC2 [NCBI] 3.53468e-06
HLA-DQB1 [NCBI] 3.52333e-06
IL1A [NCBI] 3.41651e-06
HLA-DRB1 [NCBI] 3.2078e-06
ICAM1 [NCBI] 2.97e-06
GSTP1 [NCBI] 2.80598e-06
IL1B [NCBI] 2.59872e-06
LAMB3 [NCBI] 2.5359e-06
APOB [NCBI] 2.43061e-06
LYN [NCBI] 2.17566e-06
G6PD [NCBI] 2.05237e-06
JAK2 [NCBI] 1.68711e-06
AFP [NCBI] 1.52617e-06
VWF [NCBI] 1.2609e-06
TNF [NCBI] 1.01359e-06
CDKN1A [NCBI] 6.39978e-07



OMIM


 OMIM Link Information
gain		 01
stomatocytosis i [NCBI] 0.00888869
DHS [NCBI] 0.00745202
stomatocytosis ii [NCBI] 0.00254756
CHAC [NCBI] 0.00142832
oslam syndrome [NCBI] 0.0012687
CDAN2 [NCBI] 0.00112579
DBA [NCBI] 0.000847992
HPP [NCBI] 0.00082175
malaria, susceptibility to [NCBI] 0.000638025
beta thalassemia, dominant inclusion body type [NCBI] 0.000581377
SPTA1 [NCBI] 0.000458388
HBFQTL2 [NCBI] 0.000455278
hemolytic anemia with thermal sensitivity of red cells [NCBI] 0.000387063
HBB [NCBI] 0.000366485
lipomatosis, multiple [NCBI] 0.000345291
sickle cell anemia [NCBI] 0.000333666
GPS [NCBI] 0.00032169
HS [NCBI] 0.000214959
HBA1 [NCBI] 0.000199573
sideroblastic anemia, autosomal [NCBI] 0.000193274
hemolytic poikilocytic anemia due to reduced ankyrin binding sites [NCBI] 0.000193274
macrocytosis, familial [NCBI] 0.000193274
ovalocytosis, hereditary hemolytic, with defective erythropoiesis [NCBI] 0.000193274
woronets trait [NCBI] 0.000193274
XK [NCBI] 0.000155648
gastritis, familial giant hypertrophic [NCBI] 0.000154028
ovalocytosis, hereditary hemolytic [NCBI] 0.000139233
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema [NCBI] 0.000139233
dyserythropoietic anemia with thrombocytopenia [NCBI] 0.000129637
renal tubular acidosis, distal, autosomal dominant [NCBI] 0.000129637
SLC4A1 [NCBI] 0.000124041
anemia, microcytic [NCBI] 0.000122508
RHN [NCBI] 0.000116834
Ge [NCBI] 0.000115043
erythroleukemia, familial [NCBI] 0.00010809
adenosine deaminase, elevated, hemolytic anemia due to [NCBI] 0.00010457
TTP [NCBI] 0.000101446
elliptocytosis, rhesus-unlinked type [NCBI] 0.000101446
EL1 [NCBI] 8.28286e-05
aHUS [NCBI] 8.13673e-05
EPB72 [NCBI] 8.12641e-05
PNKD1 [NCBI] 7.99807e-05
SPTB [NCBI] 6.61344e-05
ABL [NCBI] 6.33891e-05
GPX1 [NCBI] 5.98478e-05
BLM [NCBI] 5.69977e-05
CHH [NCBI] 5.48295e-05
APOB [NCBI] 4.02191e-05
PRDM16 [NCBI] 3.87672e-05
LCAT [NCBI] 3.44506e-05
EPO [NCBI] 3.38916e-05
SLE [NCBI] 3.35538e-05
Ss [NCBI] 3.33879e-05
HBA2 [NCBI] 2.90076e-05
RECQL3 [NCBI] 2.75356e-05
transcobalamin ii deficiency [NCBI] 2.75356e-05
MN [NCBI] 2.66028e-05
FY [NCBI] 2.6043e-05
GATA1 [NCBI] 2.55243e-05
porphyria cutanea tarda [NCBI] 2.3764e-05
CD47 [NCBI] 2.17492e-05
G6PD [NCBI] 1.36065e-05
ADA [NCBI] 1.25977e-05
TNF [NCBI] 8.14288e-06
AFP [NCBI] 1.28891e-06



Database Center for Life Science