|
OMIM |
Link |
Information gain |
01 |
|
stomatocytosis i
|
[NCBI]
|
0.00507112
|
|
|
DHS
|
[NCBI]
|
0.00402523
|
|
|
G6PD
|
[NCBI]
|
0.00247346
|
|
|
red cell phospholipid defect with hemolysis
|
[NCBI]
|
0.0022037
|
|
|
HBB
|
[NCBI]
|
0.00176415
|
|
|
pyruvate kinase deficiency of red cells
|
[NCBI]
|
0.00111528
|
|
|
6-@phosphogluconolactonase deficiency
|
[NCBI]
|
0.000975838
|
|
|
SLEH1
|
[NCBI]
|
0.000975838
|
|
|
TTP
|
[NCBI]
|
0.000668735
|
|
|
hyperbilirubinemia, rotor type
|
[NCBI]
|
0.000583695
|
|
|
aHUS
|
[NCBI]
|
0.000538359
|
|
|
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|
[NCBI]
|
0.000366657
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.0003621
|
|
|
HS
|
[NCBI]
|
0.000352279
|
|
|
gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to
|
[NCBI]
|
0.000339298
|
|
|
adenosine deaminase, elevated, hemolytic anemia due to
|
[NCBI]
|
0.000326926
|
|
|
PKLR
|
[NCBI]
|
0.000324215
|
|
|
HBFQTL2
|
[NCBI]
|
0.000323134
|
|
|
PGK1
|
[NCBI]
|
0.000308792
|
|
|
NT5C3
|
[NCBI]
|
0.00027229
|
|
|
RHN
|
[NCBI]
|
0.000257868
|
|
|
RA
|
[NCBI]
|
0.000250518
|
|
|
EPB42
|
[NCBI]
|
0.00022334
|
|
|
GPI
|
[NCBI]
|
0.000215465
|
|
|
heinz body anemias
|
[NCBI]
|
0.000208132
|
|
|
hemoglobin--variants for which the chain carrying the mutation is unknown or uncertain
|
[NCBI]
|
0.000208089
|
|
|
AK1
|
[NCBI]
|
0.000196975
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
0.000194735
|
|
|
RHCE
|
[NCBI]
|
0.000189661
|
|
|
IPEX
|
[NCBI]
|
0.000173222
|
|
|
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to
|
[NCBI]
|
0.000153661
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
0.000146327
|
|
|
Ii
|
[NCBI]
|
0.000135363
|
|
|
hexokinase deficiency hemolytic anemia
|
[NCBI]
|
0.000127224
|
|
|
CF
|
[NCBI]
|
0.000120234
|
|
|
SPTA1
|
[NCBI]
|
0.000107307
|
|
|
SLC4A1
|
[NCBI]
|
0.000106621
|
|
|
VEGF
|
[NCBI]
|
0.000106504
|
|
|
diphosphoglycerate mutase deficiency of erythrocyte
|
[NCBI]
|
0.000106476
|
|
|
anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism
|
[NCBI]
|
0.00010401
|
|
|
anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane
|
[NCBI]
|
0.00010401
|
|
|
hemolytic poikilocytic anemia due to reduced ankyrin binding sites
|
[NCBI]
|
0.00010401
|
|
|
spastic paraplegia and evans syndrome
|
[NCBI]
|
0.00010401
|
|
|
ovalocytosis, hereditary hemolytic, with defective erythropoiesis
|
[NCBI]
|
0.00010401
|
|
|
EL1
|
[NCBI]
|
0.000100014
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
9.57602e-05
|
|
|
HBA2
|
[NCBI]
|
9.35504e-05
|
|
|
EPB72
|
[NCBI]
|
9.20435e-05
|
|
|
GSR
|
[NCBI]
|
8.79075e-05
|
|
|
EPO
|
[NCBI]
|
8.69008e-05
|
|
|
glycogen storage disease vii
|
[NCBI]
|
8.56675e-05
|
|
|
acetophenetidin sensitivity
|
[NCBI]
|
8.15639e-05
|
|
|
ataxic diplegia with defective cellular immunity
|
[NCBI]
|
8.15639e-05
|
|
|
SLE
|
[NCBI]
|
7.977e-05
|
|
|
ovalocytosis, hereditary hemolytic
|
[NCBI]
|
7.31081e-05
|
|
|
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema
|
[NCBI]
|
6.76263e-05
|
|
|
spherocytosis, autosomal recessive
|
[NCBI]
|
6.35567e-05
|
|
|
gastritis, familial giant hypertrophic
|
[NCBI]
|
6.35567e-05
|
|
|
pernicious anemia
|
[NCBI]
|
6.35567e-05
|
|
|
cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly
|
[NCBI]
|
6.35567e-05
|
|
|
XKRX
|
[NCBI]
|
6.27014e-05
|
|
|
RHAG
|
[NCBI]
|
6.27014e-05
|
|
|
XKR3
|
[NCBI]
|
6.27014e-05
|
|
|
TPI1
|
[NCBI]
|
6.21919e-05
|
|
|
CD47
|
[NCBI]
|
6.01313e-05
|
|
|
ADAMTS13
|
[NCBI]
|
6.01313e-05
|
|
|
SPTB
|
[NCBI]
|
5.91785e-05
|
|
|
ADA
|
[NCBI]
|
5.39206e-05
|
|
|
elliptocytosis, rhesus-unlinked type
|
[NCBI]
|
5.33286e-05
|
|
|
glutathione synthetase deficiency
|
[NCBI]
|
5.15501e-05
|
|
|
PTPNS1
|
[NCBI]
|
4.89388e-05
|
|
|
SPTAN1
|
[NCBI]
|
4.89388e-05
|
|
|
GCLC
|
[NCBI]
|
4.89388e-05
|
|
|
wilson disease
|
[NCBI]
|
4.86516e-05
|
|
|
HBA1
|
[NCBI]
|
4.77845e-05
|
|
|
sitosterolemia
|
[NCBI]
|
4.37682e-05
|
|
|
ANK3
|
[NCBI]
|
4.37554e-05
|
|
|
gilbert syndrome
|
[NCBI]
|
3.86212e-05
|
|
|
CYP1A2
|
[NCBI]
|
3.79021e-05
|
|
|
PRDX2
|
[NCBI]
|
3.79021e-05
|
|
|
PGP
|
[NCBI]
|
3.59185e-05
|
|
|
PRDX1
|
[NCBI]
|
3.59185e-05
|
|
|
PGD
|
[NCBI]
|
3.59185e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
3.319e-05
|
|
|
GSS
|
[NCBI]
|
3.28652e-05
|
|
|
megaloblastic anemia 1
|
[NCBI]
|
3.22132e-05
|
|
|
PNKD1
|
[NCBI]
|
3.22132e-05
|
|
|
RHD
|
[NCBI]
|
3.16375e-05
|
|
|
ADD1
|
[NCBI]
|
3.05488e-05
|
|
|
HK1
|
[NCBI]
|
3.05488e-05
|
|
|
GSTP1
|
[NCBI]
|
2.57881e-05
|
|
|
GPX1
|
[NCBI]
|
2.57881e-05
|
|
|
HBG2
|
[NCBI]
|
2.4083e-05
|
|
|
ACADS
|
[NCBI]
|
2.1795e-05
|
|
|
MPO
|
[NCBI]
|
1.72118e-05
|
|
|
ALPS
|
[NCBI]
|
1.50562e-05
|
|
|
FOXP3
|
[NCBI]
|
1.50443e-05
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
1.4502e-05
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
1.30638e-05
|
|
|
AVP
|
[NCBI]
|
1.03682e-05
|
|
|
CHS
|
[NCBI]
|
7.16274e-06
|
|
|
CAT
|
[NCBI]
|
3.57709e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
3.32891e-06
|
|
|
AT
|
[NCBI]
|
2.52998e-06
|
|
|
F3
|
[NCBI]
|
2.3837e-06
|
|
|
CVID
|
[NCBI]
|
2.24764e-06
|
|
|
SOD2
|
[NCBI]
|
6.17379e-07
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
6.01019e-07
|
|
|
TFPI
|
[NCBI]
|
4.38635e-07
|
|
|
ACHE
|
[NCBI]
|
2.75799e-07
|
|