|
OMIM |
Link |
Information gain |
01 |
|
stomatocytosis i
|
[NCBI]
|
0.00438142
|
|
|
G6PD
|
[NCBI]
|
0.00293223
|
|
|
DHS
|
[NCBI]
|
0.00252125
|
|
|
CDAN2
|
[NCBI]
|
0.00252125
|
|
|
red cell phospholipid defect with hemolysis
|
[NCBI]
|
0.00147804
|
|
|
CDAN3
|
[NCBI]
|
0.001369251
|
|
|
CTS1
|
[NCBI]
|
0.001178484
|
|
|
pyruvate kinase deficiency of red cells
|
[NCBI]
|
0.000509428
|
|
|
HBB
|
[NCBI]
|
0.000487369
|
|
|
EL1
|
[NCBI]
|
0.000429516
|
|
|
CP
|
[NCBI]
|
0.000383314
|
|
|
glycogen storage disease vii
|
[NCBI]
|
0.000375548
|
|
|
CD59
|
[NCBI]
|
0.000366549
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000335034
|
|
|
complement factor i deficiency
|
[NCBI]
|
0.000324903
|
|
|
elliptocytosis, rhesus-unlinked type
|
[NCBI]
|
0.000320564
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
0.000295919
|
|
|
complement component 7 deficiency
|
[NCBI]
|
0.000293932
|
|
|
C3
|
[NCBI]
|
0.000281067
|
|
|
anemia, dyserythropoietic congenital, type i
|
[NCBI]
|
0.000276804
|
|
|
complement component 6 deficiency
|
[NCBI]
|
0.00026812
|
|
|
porphyria, congenital erythropoietic
|
[NCBI]
|
0.000249336
|
|
|
ovalocytosis, hereditary hemolytic, with defective erythropoiesis
|
[NCBI]
|
0.000246333
|
|
|
SLE
|
[NCBI]
|
0.0002456682
|
|
|
HP
|
[NCBI]
|
0.0002357339
|
|
|
acetophenetidin sensitivity
|
[NCBI]
|
0.000223876
|
|
|
complement component 8 deficiency, type i
|
[NCBI]
|
0.0002046641
|
|
|
C9
|
[NCBI]
|
0.0002026362
|
|
|
ABL
|
[NCBI]
|
0.0001893395
|
|
|
FDD
|
[NCBI]
|
0.0001876609
|
|
|
sickle cell anemia
|
[NCBI]
|
0.0001872261
|
|
|
HS
|
[NCBI]
|
0.0001868414
|
|
|
GPX1
|
[NCBI]
|
0.0001806066
|
|
|
thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis
|
[NCBI]
|
0.0001772022
|
|
|
complement component 4, partial deficiency of
|
[NCBI]
|
0.000170419
|
|
|
C4A
|
[NCBI]
|
0.0001678876
|
|
|
angioid streaks
|
[NCBI]
|
0.00016763
|
|
|
FBD
|
[NCBI]
|
0.0001649267
|
|
|
pseudohyperkalemia cardiff
|
[NCBI]
|
0.0001649267
|
|
|
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly
|
[NCBI]
|
0.0001608468
|
|
|
phosphorylase kinase deficiency of liver and muscle, autosomal recessive
|
[NCBI]
|
0.0001575987
|
|
|
PLB1
|
[NCBI]
|
0.0001571057
|
|
|
MCP
|
[NCBI]
|
0.0001513818
|
|
|
RHN
|
[NCBI]
|
0.0001431355
|
|
|
hexokinase deficiency hemolytic anemia
|
[NCBI]
|
0.0001310769
|
|
|
Ii
|
[NCBI]
|
0.0001306928
|
|
|
renal tubular acidosis, distal, autosomal dominant
|
[NCBI]
|
0.0001210264
|
|
|
properdin deficiency, x-linked
|
[NCBI]
|
0.000112417
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
0.0001113142
|
|
|
hyperlipoproteinemia, type i
|
[NCBI]
|
0.0001081953
|
|
|
CFI
|
[NCBI]
|
0.0001044102
|
|
|
EPO
|
[NCBI]
|
0.0001031513
|
|
|
C1RL
|
[NCBI]
|
9.64856e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
9.25724e-05
|
|
|
OPTB1
|
[NCBI]
|
9.17786e-05
|
|
|
CHAC
|
[NCBI]
|
9.14001e-05
|
|
|
C1QBP
|
[NCBI]
|
8.86734e-05
|
|
|
DKC
|
[NCBI]
|
8.40252e-05
|
|
|
EGF
|
[NCBI]
|
8.39336e-05
|
|
|
PGK1
|
[NCBI]
|
8.00125e-05
|
|
|
HBA1
|
[NCBI]
|
7.69449e-05
|
|
|
aHUS
|
[NCBI]
|
7.38838e-05
|
|
|
galactosemia
|
[NCBI]
|
7.05188e-05
|
|
|
ART4
|
[NCBI]
|
7.00596e-05
|
|
|
SLC4A1
|
[NCBI]
|
6.90434e-05
|
|
|
C4BPA
|
[NCBI]
|
6.8797e-05
|
|
|
PHKB
|
[NCBI]
|
6.53726e-05
|
|
|
CSMD1
|
[NCBI]
|
6.50597e-05
|
|
|
methemoglobinemia due to deficiency of cytochrome b5
|
[NCBI]
|
6.45257e-05
|
|
|
CAT
|
[NCBI]
|
6.43805e-05
|
|
|
complement component c1r deficiency
|
[NCBI]
|
6.3786e-05
|
|
|
TNF
|
[NCBI]
|
6.28074e-05
|
|
|
ACHE
|
[NCBI]
|
5.98913e-05
|
|
|
NT5C3
|
[NCBI]
|
5.83974e-05
|
|
|
NFE2L2
|
[NCBI]
|
5.76577e-05
|
|
|
CFD
|
[NCBI]
|
5.50027e-05
|
|
|
ARG1
|
[NCBI]
|
5.4467e-05
|
|
|
ALDOA
|
[NCBI]
|
5.16788e-05
|
|
|
PTH
|
[NCBI]
|
4.86111e-05
|
|
|
PFC
|
[NCBI]
|
4.85268e-05
|
|
|
HBZ
|
[NCBI]
|
4.66787e-05
|
|
|
EPB41
|
[NCBI]
|
4.60796e-05
|
|
|
C5
|
[NCBI]
|
4.59298e-05
|
|
|
EPB42
|
[NCBI]
|
4.59298e-05
|
|
|
RHCE
|
[NCBI]
|
4.59175e-05
|
|
|
ADAMTS13
|
[NCBI]
|
4.07504e-05
|
|
|
SLC40A1
|
[NCBI]
|
4.01453e-05
|
|
|
EGFR
|
[NCBI]
|
3.99944e-05
|
|
|
KLF1
|
[NCBI]
|
3.89467e-05
|
|
|
CFB
|
[NCBI]
|
3.7304e-05
|
|
|
PRF1
|
[NCBI]
|
3.52134e-05
|
|
|
PRL
|
[NCBI]
|
3.41979e-05
|
|
|
GPI
|
[NCBI]
|
3.35781e-05
|
|
|
XDH
|
[NCBI]
|
3.3465e-05
|
|
|
PKLR
|
[NCBI]
|
3.32707e-05
|
|
|
PIGA
|
[NCBI]
|
3.30109e-05
|
|
|
NGFB
|
[NCBI]
|
3.1949e-05
|
|
|
GSR
|
[NCBI]
|
3.19053e-05
|
|
|
ARNT
|
[NCBI]
|
3.092184e-05
|
|
|
HBD
|
[NCBI]
|
2.96192e-05
|
|
|
HRG
|
[NCBI]
|
2.928614e-05
|
|
|
methemoglobinemia due to deficiency of methemoglobin reductase
|
[NCBI]
|
2.7689e-05
|
|
|
MBL2
|
[NCBI]
|
2.76251e-05
|
|
|
PCNA
|
[NCBI]
|
2.718977e-05
|
|
|
CLU
|
[NCBI]
|
2.520923e-05
|
|
|
TLR9
|
[NCBI]
|
2.287887e-05
|
|
|
AD
|
[NCBI]
|
2.191408e-05
|
|
|
RA
|
[NCBI]
|
2.116187e-05
|
|
|
CPB2
|
[NCBI]
|
2.096034e-05
|
|
|
NGFR
|
[NCBI]
|
1.793524e-05
|
|
|
MPO
|
[NCBI]
|
1.748588e-05
|
|
|
CFH
|
[NCBI]
|
1.702977e-05
|
|
|
APOE
|
[NCBI]
|
1.382124e-05
|
|
|
CRC
|
[NCBI]
|
1.334319e-05
|
|
|
TF
|
[NCBI]
|
1.330606e-05
|
|
|
TH
|
[NCBI]
|
1.108116e-05
|
|
|
APRT
|
[NCBI]
|
1.087049e-05
|
|
|
HEMB
|
[NCBI]
|
1.03409e-05
|
|
|
SDC2
|
[NCBI]
|
1.021445e-05
|
|
|
MB
|
[NCBI]
|
9.44132e-06
|
|
|
HGF
|
[NCBI]
|
8.96073e-06
|
|
|
APOB
|
[NCBI]
|
7.44322e-06
|
|
|
LPL
|
[NCBI]
|
4.87325e-06
|
|
|
MG
|
[NCBI]
|
2.636725e-06
|
|
|
PF4
|
[NCBI]
|
2.54694e-06
|
|
|
AHR
|
[NCBI]
|
1.888141e-06
|
|
|
ALB
|
[NCBI]
|
1.870743e-06
|
|
|
CF
|
[NCBI]
|
1.689775e-06
|
|
|
CFTR
|
[NCBI]
|
7.87441e-08
|
|