|
OMIM |
Link |
Information gain |
01 |
|
EPO
|
[NCBI]
|
0.00571332
|
|
|
CDAN3
|
[NCBI]
|
0.00286856
|
|
|
adenosine triphosphatase deficiency, anemia due to
|
[NCBI]
|
0.0020554
|
|
|
DHS
|
[NCBI]
|
0.00204393
|
|
|
stomatocytosis ii
|
[NCBI]
|
0.0015337
|
|
|
transient erythroblastopenia of childhood
|
[NCBI]
|
0.0015337
|
|
|
valinemia
|
[NCBI]
|
0.00133777
|
|
|
HBB
|
[NCBI]
|
0.00128326
|
|
|
neutropenia, chronic familial
|
[NCBI]
|
0.0012111
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.0012111
|
|
|
HBFQTL4
|
[NCBI]
|
0.0012111
|
|
|
red cell phospholipid defect with hemolysis
|
[NCBI]
|
0.00104288
|
|
|
myopathy with deficiency of succinate dehydrogenase and aconitase
|
[NCBI]
|
0.000981264
|
|
|
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain
|
[NCBI]
|
0.000906176
|
|
|
MB
|
[NCBI]
|
0.00077729
|
|
|
restless legs syndrome, susceptibility to, 1
|
[NCBI]
|
0.000690808
|
|
|
HP
|
[NCBI]
|
0.000680807
|
|
|
stomatocytosis i
|
[NCBI]
|
0.000645198
|
|
|
HBFQTL2
|
[NCBI]
|
0.00048225
|
|
|
HBA1
|
[NCBI]
|
0.000452093
|
|
|
sickle cell anemia
|
[NCBI]
|
0.000336988
|
|
|
erythrocytosis, familial, 1
|
[NCBI]
|
0.000254001
|
|
|
ALB
|
[NCBI]
|
0.000230742
|
|
|
G6PD
|
[NCBI]
|
0.000226007
|
|
|
beta thalassemia, dominant inclusion body type
|
[NCBI]
|
0.000198993
|
|
|
HBFQTL1
|
[NCBI]
|
0.000195091
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.00018329
|
|
|
HBA2
|
[NCBI]
|
0.000171894
|
|
|
EGF
|
[NCBI]
|
0.000163732
|
|
|
erythrocytosis, familial, 2
|
[NCBI]
|
0.000148921
|
|
|
HBD
|
[NCBI]
|
0.000143075
|
|
|
ovalocytosis, hereditary hemolytic
|
[NCBI]
|
0.000137682
|
|
|
sulfhemoglobinemia, congenital
|
[NCBI]
|
0.000137682
|
|
|
ECYT4
|
[NCBI]
|
0.000137682
|
|
|
woronets trait
|
[NCBI]
|
0.000137682
|
|
|
RA
|
[NCBI]
|
0.000133898
|
|
|
LPI
|
[NCBI]
|
0.000124462
|
|
|
porphyria, congenital erythropoietic
|
[NCBI]
|
0.000123863
|
|
|
DBA
|
[NCBI]
|
0.000122121
|
|
|
CAT
|
[NCBI]
|
0.000116123
|
|
|
TF
|
[NCBI]
|
0.000106751
|
|
|
NGFB
|
[NCBI]
|
9.46349e-05
|
|
|
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema
|
[NCBI]
|
9.42749e-05
|
|
|
ATMDS
|
[NCBI]
|
9.42749e-05
|
|
|
IDDM
|
[NCBI]
|
8.61178e-05
|
|
|
CHH
|
[NCBI]
|
8.58696e-05
|
|
|
CF
|
[NCBI]
|
8.10209e-05
|
|
|
renal tubular acidosis, distal, with hemolytic anemia
|
[NCBI]
|
8.08818e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
7.80965e-05
|
|
|
EGFR
|
[NCBI]
|
7.46942e-05
|
|
|
PRL
|
[NCBI]
|
7.46913e-05
|
|
|
anemia, sideroblastic, x-linked
|
[NCBI]
|
7.0349e-05
|
|
|
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to
|
[NCBI]
|
6.9373e-05
|
|
|
amyloidosis, familial visceral
|
[NCBI]
|
6.9373e-05
|
|
|
MCPH1
|
[NCBI]
|
6.65711e-05
|
|
|
HBZ
|
[NCBI]
|
6.58496e-05
|
|
|
myeloma, multiple
|
[NCBI]
|
6.40879e-05
|
|
|
formiminotransferase deficiency
|
[NCBI]
|
6.18594e-05
|
|
|
CEACAM5
|
[NCBI]
|
5.72342e-05
|
|
|
CRH
|
[NCBI]
|
5.64242e-05
|
|
|
hypoascorbemia
|
[NCBI]
|
5.62912e-05
|
|
|
JH
|
[NCBI]
|
5.62912e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
5.47161e-05
|
|
|
GFAP
|
[NCBI]
|
5.42272e-05
|
|
|
SLC40A1
|
[NCBI]
|
5.37834e-05
|
|
|
HBE1
|
[NCBI]
|
5.3377e-05
|
|
|
aceruloplasminemia
|
[NCBI]
|
5.18787e-05
|
|
|
SLC4A1
|
[NCBI]
|
5.12872e-05
|
|
|
TH
|
[NCBI]
|
5.11784e-05
|
|
|
ERAF
|
[NCBI]
|
5.0601e-05
|
|
|
OPTB1
|
[NCBI]
|
5.05915e-05
|
|
|
INHBA
|
[NCBI]
|
4.96857e-05
|
|
|
hyperlipoproteinemia, type i
|
[NCBI]
|
4.82331e-05
|
|
|
EL1
|
[NCBI]
|
4.71473e-05
|
|
|
PCNA
|
[NCBI]
|
4.61052e-05
|
|
|
BDNF
|
[NCBI]
|
4.60637e-05
|
|
|
gaucher disease, type iii
|
[NCBI]
|
4.41967e-05
|
|
|
CHAC
|
[NCBI]
|
4.16207e-05
|
|
|
VIP
|
[NCBI]
|
4.07412e-05
|
|
|
OCA1A
|
[NCBI]
|
4.00706e-05
|
|
|
VWS
|
[NCBI]
|
4.00706e-05
|
|
|
SCIDX1
|
[NCBI]
|
4.00706e-05
|
|
|
malaria, susceptibility to
|
[NCBI]
|
4.00706e-05
|
|
|
APOE
|
[NCBI]
|
3.52488e-05
|
|
|
TNF
|
[NCBI]
|
3.43118e-05
|
|
|
HBG1
|
[NCBI]
|
3.39378e-05
|
|
|
HPR
|
[NCBI]
|
3.18028e-05
|
|
|
LPL
|
[NCBI]
|
3.12219e-05
|
|
|
thrombocytosis, familial x-linked
|
[NCBI]
|
2.97704e-05
|
|
|
growth hormone insensitivity syndrome
|
[NCBI]
|
2.94568e-05
|
|
|
HGF
|
[NCBI]
|
2.61449e-05
|
|
|
KLF1
|
[NCBI]
|
2.59778e-05
|
|
|
JMML
|
[NCBI]
|
2.43277e-05
|
|
|
CYGB
|
[NCBI]
|
2.40699e-05
|
|
|
SEC15L1
|
[NCBI]
|
2.23675e-05
|
|
|
AFP
|
[NCBI]
|
2.11641e-05
|
|
|
SLC11A2
|
[NCBI]
|
2.10126e-05
|
|
|
menkes disease
|
[NCBI]
|
1.99239e-05
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
1.96859e-05
|
|
|
MN
|
[NCBI]
|
1.91752e-05
|
|
|
CRC
|
[NCBI]
|
1.90964e-05
|
|
|
SLE
|
[NCBI]
|
1.82917e-05
|
|
|
EPOR
|
[NCBI]
|
1.78911e-05
|
|
|
NGB
|
[NCBI]
|
1.78086e-05
|
|
|
hemoglobin--alpha locus 3
|
[NCBI]
|
1.77873e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
1.72929e-05
|
|
|
KLK3
|
[NCBI]
|
1.72378e-05
|
|
|
temporal arteritis
|
[NCBI]
|
1.71827e-05
|
|
|
ALPS
|
[NCBI]
|
1.54205e-05
|
|
|
CD163
|
[NCBI]
|
1.53973e-05
|
|
|
AD
|
[NCBI]
|
1.50246e-05
|
|
|
TG
|
[NCBI]
|
1.4575e-05
|
|
|
CAMK4
|
[NCBI]
|
1.45213e-05
|
|
|
ADD2
|
[NCBI]
|
1.45213e-05
|
|
|
HMOX2
|
[NCBI]
|
1.45213e-05
|
|
|
PRDX1
|
[NCBI]
|
1.31239e-05
|
|
|
HBQ1
|
[NCBI]
|
1.31239e-05
|
|
|
VRK1
|
[NCBI]
|
1.31239e-05
|
|
|
PXE
|
[NCBI]
|
1.1796e-05
|
|
|
VEGF
|
[NCBI]
|
1.16066e-05
|
|
|
GSS
|
[NCBI]
|
1.15657e-05
|
|
|
HEPH
|
[NCBI]
|
1.00492e-05
|
|
|
EPAS1
|
[NCBI]
|
1.00492e-05
|
|
|
SHBG
|
[NCBI]
|
8.98149e-06
|
|
|
GPI
|
[NCBI]
|
8.84178e-06
|
|
|
BWS
|
[NCBI]
|
8.46576e-06
|
|
|
SPP1
|
[NCBI]
|
8.25082e-06
|
|
|
CA2
|
[NCBI]
|
8.19759e-06
|
|
|
PTH
|
[NCBI]
|
8.15291e-06
|
|
|
VDR
|
[NCBI]
|
8.07533e-06
|
|
|
CA1
|
[NCBI]
|
7.78282e-06
|
|
|
CPM
|
[NCBI]
|
7.78282e-06
|
|
|
AHR
|
[NCBI]
|
7.60781e-06
|
|
|
FMF
|
[NCBI]
|
7.43186e-06
|
|
|
RBP3
|
[NCBI]
|
6.29311e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
6.26563e-06
|
|
|
GPX1
|
[NCBI]
|
6.15625e-06
|
|
|
ACP1
|
[NCBI]
|
5.89577e-06
|
|
|
TIMP1
|
[NCBI]
|
5.89577e-06
|
|
|
PTX3
|
[NCBI]
|
5.77168e-06
|
|
|
ATRX
|
[NCBI]
|
5.4215e-06
|
|
|
HIF1A
|
[NCBI]
|
5.31153e-06
|
|
|
FY
|
[NCBI]
|
5.31153e-06
|
|
|
coproporphyria
|
[NCBI]
|
5.20468e-06
|
|
|
AVP
|
[NCBI]
|
5.05225e-06
|
|
|
TNFRSF6
|
[NCBI]
|
4.90137e-06
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
4.71232e-06
|
|
|
MAPK14
|
[NCBI]
|
4.71232e-06
|
|
|
XDH
|
[NCBI]
|
4.68237e-06
|
|
|
ACHE
|
[NCBI]
|
4.67116e-06
|
|
|
HS
|
[NCBI]
|
4.36197e-06
|
|
|
GSR
|
[NCBI]
|
4.36197e-06
|
|
|
PKD2
|
[NCBI]
|
4.04402e-06
|
|
|
ALAD
|
[NCBI]
|
4.04402e-06
|
|
|
HFE
|
[NCBI]
|
4.00132e-06
|
|
|
NAT1
|
[NCBI]
|
3.89575e-06
|
|
|
MDD
|
[NCBI]
|
3.88794e-06
|
|
|
DAO
|
[NCBI]
|
3.75397e-06
|
|
|
TFPI
|
[NCBI]
|
3.61128e-06
|
|
|
methemoglobinemia due to deficiency of methemoglobin reductase
|
[NCBI]
|
3.55252e-06
|
|
|
HBG2
|
[NCBI]
|
3.42516e-06
|
|
|
amyloidosis vi
|
[NCBI]
|
3.42111e-06
|
|
|
NP
|
[NCBI]
|
3.36343e-06
|
|
|
NPPA
|
[NCBI]
|
3.34205e-06
|
|
|
PRLH
|
[NCBI]
|
2.91159e-06
|
|
|
SOD2
|
[NCBI]
|
2.88396e-06
|
|
|
APOD
|
[NCBI]
|
2.80914e-06
|
|
|
ADA
|
[NCBI]
|
2.73526e-06
|
|
|
F2R
|
[NCBI]
|
2.61532e-06
|
|
|
CP
|
[NCBI]
|
2.60632e-06
|
|
|
factor v deficiency
|
[NCBI]
|
2.52358e-06
|
|
|
CYP1A1
|
[NCBI]
|
2.5019e-06
|
|
|
BTK
|
[NCBI]
|
2.47894e-06
|
|
|
CTGF
|
[NCBI]
|
2.22547e-06
|
|
|
GAPDH
|
[NCBI]
|
2.02105e-06
|
|
|
NMB
|
[NCBI]
|
1.86025e-06
|
|
|
PAEP
|
[NCBI]
|
1.66757e-06
|
|
|
F3
|
[NCBI]
|
1.53974e-06
|
|
|
ACE
|
[NCBI]
|
1.47666e-06
|
|
|
ESD
|
[NCBI]
|
1.16554e-06
|
|
|
CD
|
[NCBI]
|
9.56449e-07
|
|
|
ACPP
|
[NCBI]
|
7.12787e-07
|
|
|
PF4
|
[NCBI]
|
6.23276e-07
|
|
|
STAT5A
|
[NCBI]
|
6.20919e-07
|
|
|
GC
|
[NCBI]
|
5.65817e-07
|
|
|
HMBS
|
[NCBI]
|
4.77603e-07
|
|
|
hemophilia a
|
[NCBI]
|
4.09749e-07
|
|
|
LRP1
|
[NCBI]
|
2.82597e-07
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.41642e-07
|
|
|
DMD
|
[NCBI]
|
1.87041e-07
|
|
|
BCR
|
[NCBI]
|
1.49979e-07
|
|
|
TNFSF10
|
[NCBI]
|
8.67815e-08
|
|
|
SERPINA6
|
[NCBI]
|
5.92539e-08
|
|
|
JAK2
|
[NCBI]
|
5.56226e-08
|
|
|
MPO
|
[NCBI]
|
3.83813e-08
|
|
|
SOD1
|
[NCBI]
|
3.01375e-08
|
|
|
TTR
|
[NCBI]
|
2.64081e-08
|
|
|
GHR
|
[NCBI]
|
2.61724e-08
|
|
|
ABP1
|
[NCBI]
|
1.96451e-08
|
|
|
GNRH1
|
[NCBI]
|
5.58484e-09
|
|
|
COMP
|
[NCBI]
|
1.24848e-09
|
|