Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


Query MeSH keywords list

01 Blood Group Antigens [NCBI]

Gene


 Gene Link Information
Gain		 01
SF [NCBI] 0.000459418
XGPY [NCBI] 0.000192906
AYP1p1 [NCBI] 0.000192906
SEC1 [NCBI] 0.000171302
AQP1 [NCBI] 0.000116589
VUR [NCBI] 7.3507e-05
AQP3 [NCBI] 4.98642e-05
AQP2 [NCBI] 4.16258e-05
XG [NCBI] 3.72819e-05
AQP4 [NCBI] 2.75332e-05
ART4 [NCBI] 2.6498e-05
UMOD [NCBI] 2.43022e-05
MS [NCBI] 2.11367e-05
SLC4A1 [NCBI] 2.1103e-05
ERMAP [NCBI] 1.8696e-05
DARC [NCBI] 1.85449e-05
GC [NCBI] 1.71364e-05
ABO [NCBI] 1.6943e-05
GYPC [NCBI] 1.60038e-05
ICAM4 [NCBI] 1.59254e-05
XK [NCBI] 1.51054e-05
ESD [NCBI] 1.43271e-05
SLC14A1 [NCBI] 1.18641e-05
CR1 [NCBI] 1.10724e-05
CD99 [NCBI] 1.03985e-05
GYPA [NCBI] 9.97948e-06
AQP5 [NCBI] 9.89151e-06
KEL [NCBI] 9.55104e-06
MIP [NCBI] 9.4455e-06
HP [NCBI] 9.3569e-06
FUT2 [NCBI] 8.96072e-06
VWF [NCBI] 8.78829e-06
B4GALNT2 [NCBI] 8.56281e-06
GYPB [NCBI] 6.97292e-06
TF [NCBI] 6.94261e-06
PGM1 [NCBI] 6.48917e-06
CD55 [NCBI] 5.75784e-06
TFRC [NCBI] 5.47797e-06
BCAM [NCBI] 4.62767e-06
CD47 [NCBI] 3.65688e-06
CD44 [NCBI] 3.07735e-06
FUT3 [NCBI] 2.96794e-06
RHD [NCBI] 2.67235e-06
ACHE [NCBI] 2.59111e-06
RHCE [NCBI] 2.54271e-06
SLC5A1 [NCBI] 2.27679e-06
TDFA [NCBI] 2.21876e-06
UMODL1 [NCBI] 1.92029e-06
SRY [NCBI] 1.83939e-06
GPSN2 [NCBI] 1.82165e-06
AQP10 [NCBI] 1.78331e-06
NOS3 [NCBI] 1.68673e-06
A4GALT [NCBI] 1.64659e-06
SEMA7A [NCBI] 1.6069e-06
B3GALNT1 [NCBI] 1.55662e-06
RPS4Y1 [NCBI] 1.54176e-06
ALB [NCBI] 1.4915e-06
FUT1 [NCBI] 1.456e-06
CCDC6 [NCBI] 1.456e-06
TAS2R38 [NCBI] 1.42629e-06
AK1 [NCBI] 1.39956e-06
ICAM5 [NCBI] 1.36764e-06
RDBP [NCBI] 1.36764e-06
HLA-DOB [NCBI] 1.35301e-06
PDPN [NCBI] 1.34598e-06
AQP9 [NCBI] 1.33914e-06
LNPEP [NCBI] 1.33914e-06
HLA-DOA [NCBI] 1.33914e-06
EPO [NCBI] 1.33247e-06
CLCN5 [NCBI] 1.3196e-06
NFYB [NCBI] 1.3014e-06
ALPI [NCBI] 1.28992e-06
NFYA [NCBI] 1.23437e-06
RHAG [NCBI] 1.20021e-06
C4A [NCBI] 1.18465e-06
NP [NCBI] 1.1809e-06
CFTR [NCBI] 1.17881e-06
MUC5AC [NCBI] 1.13959e-06
C4B [NCBI] 1.12411e-06
CEL [NCBI] 1.11524e-06
LAMP2 [NCBI] 1.10386e-06
S100A7 [NCBI] 1.08505e-06
CCL8 [NCBI] 1.08247e-06
LAMP1 [NCBI] 1.07239e-06
CD151 [NCBI] 1.06749e-06
ITGAL [NCBI] 1.05796e-06
MME [NCBI] 1.04651e-06
CTSA [NCBI] 1.02294e-06
SIGLEC1 [NCBI] 1.01289e-06
S100A6 [NCBI] 1.01289e-06
PTX3 [NCBI] 9.97566e-07
CD59 [NCBI] 9.77855e-07
F13A1 [NCBI] 9.69362e-07
CXCL5 [NCBI] 9.43898e-07
CCL21 [NCBI] 9.27726e-07
PAX2 [NCBI] 9.26305e-07
CCL7 [NCBI] 9.24891e-07
PROC [NCBI] 9.20694e-07
SELE [NCBI] 9.08493e-07
ITGB2 [NCBI] 8.9182e-07
CCL17 [NCBI] 8.60269e-07
ICAM3 [NCBI] 8.45303e-07
C1QBP [NCBI] 8.42205e-07
CD93 [NCBI] 8.32139e-07
ATXN1 [NCBI] 8.30172e-07
PRKD1 [NCBI] 7.95392e-07
APOD [NCBI] 7.91146e-07
PAEP [NCBI] 7.47139e-07
DAG1 [NCBI] 7.47139e-07
CCL5 [NCBI] 7.32661e-07
DCT [NCBI] 7.28012e-07
HBB [NCBI] 7.22801e-07
KRT7 [NCBI] 7.10838e-07
GATA1 [NCBI] 6.93601e-07
CP [NCBI] 6.90745e-07
PAH [NCBI] 6.88482e-07
EPB41L1 [NCBI] 6.80721e-07
MUC2 [NCBI] 6.6383e-07
EPB41L2 [NCBI] 6.58776e-07
SELPLG [NCBI] 6.58276e-07
F8 [NCBI] 6.51868e-07
CXCL1 [NCBI] 6.50897e-07
PKD1 [NCBI] 6.41852e-07
ADAMTS13 [NCBI] 6.29093e-07
HNF1A [NCBI] 6.23384e-07
INS [NCBI] 6.06603e-07
RET [NCBI] 5.93953e-07
SLC2A4 [NCBI] 5.89751e-07
BTK [NCBI] 5.8824e-07
TFPI [NCBI] 5.84134e-07
F2 [NCBI] 5.77559e-07
F5 [NCBI] 5.71157e-07
XRCC5 [NCBI] 5.6698e-07
HLA-A [NCBI] 5.62197e-07
SLC2A1 [NCBI] 5.41145e-07
CTGF [NCBI] 5.0124e-07
TJP1 [NCBI] 4.86984e-07
CCL2 [NCBI] 4.75418e-07
G6PD [NCBI] 4.44642e-07
CETP [NCBI] 4.18432e-07
ADA [NCBI] 4.16425e-07
MTHFR [NCBI] 3.98957e-07
AFP [NCBI] 2.41671e-07
AR [NCBI] 2.11537e-07
EGFR [NCBI] 1.06609e-07



OMIM


 OMIM Link Information
gain		 01
blood group--lutheran inhibitor [NCBI] 0.00387299
MF4 [NCBI] 0.00179948
UL [NCBI] 0.00179948
LKE [NCBI] 0.00179948
fingerprints, absence of [NCBI] 0.00179948
acromial dimples [NCBI] 0.00179948
spatial visualization, aptitude for [NCBI] 0.00179948
lipoprotein types--ld system [NCBI] 0.00179948
adenosine triphosphatase deficiency, anemia due to [NCBI] 0.00179948
hyperpigmentation, familial progressive [NCBI] 0.00179948
Sf [NCBI] 0.00179948
AN [NCBI] 0.00179948
salivary substance, clostridium botulinum type [NCBI] 0.00179948
koilonychia, hereditary [NCBI] 0.00179948
letterer-siwe disease [NCBI] 0.00179948
molar i reinclusion [NCBI] 0.00127937
AKE [NCBI] 0.00127937
ASD1 [NCBI] 0.00127937
thrombasthenia-thrombocytopenia, hereditary [NCBI] 0.00127937
MAFD2 [NCBI] 0.00121196
renal failure, progressive, with hypertension [NCBI] 0.00108503
precocious puberty [NCBI] 0.00108503
cowchock syndrome [NCBI] 0.00108503
xm system [NCBI] 0.00108503
OPA2 [NCBI] 0.00108503
blood group, p system [NCBI] 0.000997767
SC [NCBI] 0.000964963
DFN2 [NCBI] 0.000959946
AQP1 [NCBI] 0.000915664
CO [NCBI] 0.000906505
OTSC1 [NCBI] 0.000867747
CDAN3 [NCBI] 0.000867747
DI [NCBI] 0.000776687
SW [NCBI] 0.000776687
RA [NCBI] 0.000661436
YT [NCBI] 0.000646976
blood group--froese [NCBI] 0.00051737
CGD [NCBI] 0.000476964
IN [NCBI] 0.000460431
CDAN2 [NCBI] 0.000414778
Ge [NCBI] 0.000393669
FY [NCBI] 0.000388017
SLE [NCBI] 0.000383237
ART4 [NCBI] 0.000345014
RD [NCBI] 0.00033669
CF [NCBI] 0.000310867
GC [NCBI] 0.000293737
XG [NCBI] 0.00029232
thiourea tasting [NCBI] 0.000281061
CZP1 [NCBI] 0.000279246
XK [NCBI] 0.000268701
alkaline phosphatase, blood group-associated [NCBI] 0.000258476
WD [NCBI] 0.000258476
Ii [NCBI] 0.000228616
ERMAP [NCBI] 0.000213353
HLA-A [NCBI] 0.000211782
raph blood group system [NCBI] 0.00019545
JK [NCBI] 0.000184629
CMT1B [NCBI] 0.000172556
VWS [NCBI] 0.000170099
ED1 [NCBI] 0.000170099
malaria, susceptibility to [NCBI] 0.000170099
RHCE [NCBI] 0.000167162
australia antigen [NCBI] 0.000156429
dystrophia myotonica 1 [NCBI] 0.000151277
RHN [NCBI] 0.000150384
KEL [NCBI] 0.00014999
THC1 [NCBI] 0.000140328
deafness, conductive, with stapes fixation [NCBI] 0.000140328
PGM1 [NCBI] 0.00013632
blood group--private systems [NCBI] 0.000129186
gil blood group [NCBI] 0.000129186
NFLD [NCBI] 0.000129186
larynx, congenital partial atresia of [NCBI] 0.000129186
lutheran null [NCBI] 0.000129186
WR [NCBI] 0.000129186
ovalocytosis, hereditary hemolytic [NCBI] 0.000129186
sc(1) trait of saliva [NCBI] 0.000129186
asthma, short stature, and elevated iga [NCBI] 0.000129186
blood group--public systems [NCBI] 0.000129186
blood group--en [NCBI] 0.000129186
woronets trait [NCBI] 0.000129186
LU [NCBI] 0.000124618
SLC4A1 [NCBI] 0.000123839
ichthyosis, x-linked [NCBI] 0.000118249
C4B [NCBI] 0.0001161
CCAL2 [NCBI] 0.000114112
DMD [NCBI] 0.000113427
OCRL [NCBI] 0.000109462
meningioma, familial [NCBI] 0.000109462
MN [NCBI] 0.0001011
CMTX1 [NCBI] 9.96765e-05
ACP1 [NCBI] 9.95116e-05
KN [NCBI] 9.76733e-05
CD99 [NCBI] 9.567e-05
FUT1 [NCBI] 9.40778e-05
HP [NCBI] 9.22282e-05
FUT2 [NCBI] 8.75379e-05
fabry disease [NCBI] 8.65614e-05
mixed lymphocyte culture locus ii [NCBI] 8.58281e-05
chromosome 18p deletion syndrome [NCBI] 8.58281e-05
surface antigen, glycoprotein 75 [NCBI] 8.58281e-05
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis [NCBI] 8.58281e-05
LW [NCBI] 8.43584e-05
HPA-2 [NCBI] 8.10375e-05
NPS [NCBI] 7.8375e-05
XS [NCBI] 7.81633e-05
AQP3 [NCBI] 7.64369e-05
CHM [NCBI] 7.44447e-05
CRS1 [NCBI] 7.2484e-05
mast cell disease [NCBI] 7.2484e-05
watson syndrome [NCBI] 7.2484e-05
CD55 [NCBI] 7.21489e-05
ND [NCBI] 7.17377e-05
SPG17 [NCBI] 6.79741e-05
HDL2 [NCBI] 6.42369e-05
SEDT [NCBI] 6.42369e-05
CMAH [NCBI] 6.42369e-05
JBS [NCBI] 6.42369e-05
C3 [NCBI] 6.35109e-05
methemoglobinemia due to deficiency of methemoglobin reductase [NCBI] 6.28105e-05
AMY2A [NCBI] 6.23432e-05
PGD [NCBI] 6.14554e-05
cryptorchidism, unilateral or bilateral [NCBI] 6.10489e-05
reifenstein syndrome [NCBI] 6.10489e-05
kuru, susceptibility to [NCBI] 6.10489e-05
pulmonary edema of mountaineers [NCBI] 6.10489e-05
hypertriglyceridemia, familial [NCBI] 5.82715e-05
DYX1 [NCBI] 5.82715e-05
IHCM [NCBI] 5.82715e-05
renal tubular acidosis, distal, autosomal dominant [NCBI] 5.82715e-05
takayasu arteritis [NCBI] 5.58129e-05
AHDS [NCBI] 5.58129e-05
VEGF [NCBI] 5.56042e-05
THC2 [NCBI] 5.36089e-05
CDPX1 [NCBI] 5.36089e-05
EDM1 [NCBI] 5.36089e-05
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 [NCBI] 5.36089e-05
B4GALNT2 [NCBI] 5.30582e-05
GPI [NCBI] 5.25681e-05
SPG2 [NCBI] 5.1613e-05
ichthyosis vulgaris [NCBI] 5.1613e-05
leopard syndrome 1 [NCBI] 4.97904e-05
IFD [NCBI] 4.97904e-05
diabetes insipidus, nephrogenic, autosomal [NCBI] 4.81144e-05
JH [NCBI] 4.81144e-05
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency [NCBI] 4.68065e-05
MADA [NCBI] 4.65639e-05
PMC [NCBI] 4.65639e-05
TTDP [NCBI] 4.65639e-05
ALB [NCBI] 4.64988e-05
C4A [NCBI] 4.61672e-05
LAG5 [NCBI] 4.55771e-05
CDG2C [NCBI] 4.51222e-05
pfeiffer syndrome [NCBI] 4.51222e-05
xanthinuria, type i [NCBI] 4.37756e-05
hyperlipoproteinemia, type ii [NCBI] 4.37756e-05
A4GALT [NCBI] 4.31912e-05
pituitary dwarfism i [NCBI] 4.2513e-05
DKC [NCBI] 4.13249e-05
FUT3 [NCBI] 4.12471e-05
kartagener syndrome [NCBI] 4.02036e-05
EL1 [NCBI] 3.91424e-05
MG [NCBI] 3.84081e-05
RP3 [NCBI] 3.71779e-05
GCPS [NCBI] 3.71779e-05
BPES [NCBI] 3.62654e-05
CCT [NCBI] 3.55209e-05
yeast factor [NCBI] 3.55209e-05
TF [NCBI] 3.4582e-05
PFIC1 [NCBI] 3.45611e-05
AHC [NCBI] 3.45611e-05
OA1 [NCBI] 3.38985e-05
CHAC [NCBI] 3.37631e-05
SPDA1 [NCBI] 3.29975e-05
CBD [NCBI] 3.26575e-05
WS1 [NCBI] 3.22621e-05
RTS [NCBI] 3.22621e-05
obesity [NCBI] 3.15548e-05
IGKC [NCBI] 3.05497e-05
RP2 [NCBI] 3.02369e-05
IGER [NCBI] 3.02171e-05
TGD [NCBI] 3.02171e-05
FCAS [NCBI] 3.02171e-05
AK1 [NCBI] 2.96386e-05
anemia, sideroblastic, x-linked [NCBI] 2.93521e-05
BMD [NCBI] 2.89715e-05
ABO [NCBI] 2.88022e-05
KAL1 [NCBI] 2.88022e-05
CLN3 [NCBI] 2.78073e-05
aHUS [NCBI] 2.61945e-05
IGHG4 [NCBI] 2.53095e-05
TBG [NCBI] 2.46844e-05
MUC1 [NCBI] 2.46779e-05
antigen defined by monoclonal antibody f10.44.2 [NCBI] 2.34969e-05
BLM [NCBI] 2.33658e-05
SLOS [NCBI] 2.30995e-05
PRKAR1B [NCBI] 2.21509e-05
MIC2Y [NCBI] 2.21509e-05
alkaline phosphatase, elevated serum [NCBI] 2.21509e-05
lynch syndrome i [NCBI] 2.13325e-05
CHE2 [NCBI] 2.10797e-05
B3GALNT1 [NCBI] 2.01901e-05
LNPEP [NCBI] 2.01901e-05
LNS [NCBI] 1.95329e-05
SEMA7A [NCBI] 1.87654e-05
PEPC [NCBI] 1.87654e-05
SCZD [NCBI] 1.85478e-05
PSORS1 [NCBI] 1.82336e-05
GCNT2 [NCBI] 1.81763e-05
SRA2 [NCBI] 1.81763e-05
PI [NCBI] 1.78649e-05
CD151 [NCBI] 1.76469e-05
Ss [NCBI] 1.76469e-05
EGFR [NCBI] 1.75566e-05
WT1 [NCBI] 1.73299e-05
OCP [NCBI] 1.73299e-05
ESD [NCBI] 1.70895e-05
CBP [NCBI] 1.67267e-05
JARID1D [NCBI] 1.59457e-05
ICAM5 [NCBI] 1.59457e-05
WRN [NCBI] 1.59421e-05
APOA2 [NCBI] 1.55955e-05
AVP [NCBI] 1.52475e-05
FCGR3A [NCBI] 1.49595e-05
PGM3 [NCBI] 1.43939e-05
NCSTN [NCBI] 1.43939e-05
CEACAM5 [NCBI] 1.41313e-05
ALPP [NCBI] 1.36486e-05
F12 [NCBI] 1.36486e-05
pta deficiency [NCBI] 1.36486e-05
RHD [NCBI] 1.34228e-05
menkes disease [NCBI] 1.33194e-05
GLO1 [NCBI] 1.28004e-05
GJA8 [NCBI] 1.28004e-05
DMD [NCBI] 1.26122e-05
ITGA2B [NCBI] 1.24248e-05
CD44 [NCBI] 1.22472e-05
phenylketonuria [NCBI] 1.18408e-05
BCNS [NCBI] 1.17103e-05
complement component 6 deficiency [NCBI] 1.14439e-05
SHOX [NCBI] 1.12979e-05
FRDA [NCBI] 1.11606e-05
APOC2 [NCBI] 1.10185e-05
fragile x mental retardation syndrome [NCBI] 1.08088e-05
AHO [NCBI] 1.04681e-05
fucosidosis [NCBI] 1.02659e-05
LPA [NCBI] 9.92992e-06
transcobalamin ii deficiency [NCBI] 9.82302e-06
HS [NCBI] 9.41822e-06
hypercholesterolemia, autosomal dominant [NCBI] 9.0607e-06
UMOD [NCBI] 8.70131e-06
PGK1 [NCBI] 8.6191e-06
APCS [NCBI] 8.45902e-06
SPTA1 [NCBI] 8.38106e-06
MTND4 [NCBI] 8.38106e-06
NP [NCBI] 8.22909e-06
AQP4 [NCBI] 8.15499e-06
HBD [NCBI] 7.73465e-06
AQP2 [NCBI] 7.47524e-06
AFP [NCBI] 7.40566e-06
BTK [NCBI] 7.11315e-06
GNAS [NCBI] 6.00224e-06
HPRT1 [NCBI] 5.13411e-06
antithrombin iii deficiency [NCBI] 5.09899e-06
ACHE [NCBI] 4.61539e-06
RB1 [NCBI] 4.51862e-06
thrombocytopenic purpura, autoimmune [NCBI] 4.4753e-06
HBB [NCBI] 3.99867e-06
hla-d histocompatibility type [NCBI] 3.9279e-06
HEMB [NCBI] 3.43505e-06
HFE [NCBI] 3.41376e-06
AIS [NCBI] 3.3938e-06
leber optic atrophy [NCBI] 2.96062e-06
FMF [NCBI] 2.56789e-06
AR [NCBI] 2.33906e-06
G6PD [NCBI] 1.98073e-06
EPO [NCBI] 1.86154e-06
IDDM [NCBI] 1.19777e-06
HBA1 [NCBI] 1.1443e-06
INS [NCBI] 1.06264e-06
ADA [NCBI] 1.00943e-06
CP [NCBI] 8.02643e-07
APOB [NCBI] 7.38284e-07
HD [NCBI] 5.33541e-07
CFTR [NCBI] 4.32639e-07
CTGF [NCBI] 1.95972e-07
WAS [NCBI] 1.07564e-07
TTR [NCBI] 1.87154e-08



Database Center for Life Science