|
OMIM |
Link |
Information gain |
01 |
|
IGAN1
|
[NCBI]
|
0.00208912
|
|
|
SLE
|
[NCBI]
|
0.00197562
|
|
|
PEE1
|
[NCBI]
|
0.00187014
|
|
|
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
|
[NCBI]
|
0.000973879
|
|
|
megaloblastic anemia 1
|
[NCBI]
|
0.000859909
|
|
|
AMRF
|
[NCBI]
|
0.000742078
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.00066179
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000654887
|
|
|
IGES
|
[NCBI]
|
0.000451673
|
|
|
fanconi renotubular syndrome
|
[NCBI]
|
0.000436268
|
|
|
ALB
|
[NCBI]
|
0.000417803
|
|
|
MCKD1
|
[NCBI]
|
0.000349925
|
|
|
CLCN5
|
[NCBI]
|
0.000309123
|
|
|
VUR1
|
[NCBI]
|
0.000307815
|
|
|
hashimoto thyroiditis
|
[NCBI]
|
0.000301869
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
0.000294478
|
|
|
FMF
|
[NCBI]
|
0.000287128
|
|
|
NPHS1
|
[NCBI]
|
0.000269002
|
|
|
lecithin:cholesterol acyltransferase deficiency
|
[NCBI]
|
0.000255321
|
|
|
CF
|
[NCBI]
|
0.000229791
|
|
|
CTGF
|
[NCBI]
|
0.000207434
|
|
|
ACE
|
[NCBI]
|
0.000203113
|
|
|
dent disease 1
|
[NCBI]
|
0.000155604
|
|
|
PCNA
|
[NCBI]
|
0.000147161
|
|
|
LCAT
|
[NCBI]
|
0.000129299
|
|
|
SDC2
|
[NCBI]
|
0.000127196
|
|
|
donnai-barrow syndrome
|
[NCBI]
|
0.000119048
|
|
|
CD2AP
|
[NCBI]
|
0.000110811
|
|
|
LRP2
|
[NCBI]
|
0.000110811
|
|
|
TF
|
[NCBI]
|
9.78721e-05
|
|
|
fabry disease
|
[NCBI]
|
9.56901e-05
|
|
|
FSGS3
|
[NCBI]
|
9.33118e-05
|
|
|
neuropathy, with paraprotein in serum, cerebrospinal fluid and urine
|
[NCBI]
|
9.33118e-05
|
|
|
SPP1
|
[NCBI]
|
8.70014e-05
|
|
|
LPG
|
[NCBI]
|
8.39084e-05
|
|
|
NPS
|
[NCBI]
|
8.34251e-05
|
|
|
VEGF
|
[NCBI]
|
7.64678e-05
|
|
|
B2M
|
[NCBI]
|
7.14924e-05
|
|
|
NPHS1
|
[NCBI]
|
6.95702e-05
|
|
|
NPHP1
|
[NCBI]
|
6.89978e-05
|
|
|
OCRL
|
[NCBI]
|
6.50115e-05
|
|
|
KIRREL
|
[NCBI]
|
6.24052e-05
|
|
|
KHDRBS3
|
[NCBI]
|
6.24052e-05
|
|
|
LR8
|
[NCBI]
|
6.24052e-05
|
|
|
HPGD
|
[NCBI]
|
6.24052e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
5.7689e-05
|
|
|
ATS
|
[NCBI]
|
5.76508e-05
|
|
|
cystinosis, late-onset juvenile or adolescent nephropathic type
|
[NCBI]
|
5.29577e-05
|
|
|
hypophosphatemic rickets, x-linked recessive
|
[NCBI]
|
5.29577e-05
|
|
|
membranoproliferative glomerulonephritis, x-linked
|
[NCBI]
|
5.29577e-05
|
|
|
AGT
|
[NCBI]
|
4.98284e-05
|
|
|
barraquer-simons syndrome
|
[NCBI]
|
4.97449e-05
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
4.97449e-05
|
|
|
ADIPOQ
|
[NCBI]
|
4.92533e-05
|
|
|
GLA
|
[NCBI]
|
4.86954e-05
|
|
|
GIPC1
|
[NCBI]
|
4.86431e-05
|
|
|
hepatocellular carcinoma-associated antigen 112
|
[NCBI]
|
4.86431e-05
|
|
|
UMOD
|
[NCBI]
|
4.76275e-05
|
|
|
KLK3
|
[NCBI]
|
4.72116e-05
|
|
|
XRN
|
[NCBI]
|
4.70818e-05
|
|
|
CAT
|
[NCBI]
|
4.68149e-05
|
|
|
hypertension, essential
|
[NCBI]
|
4.51173e-05
|
|
|
AMBP
|
[NCBI]
|
4.34603e-05
|
|
|
MAP3K7
|
[NCBI]
|
4.34603e-05
|
|
|
NOS3
|
[NCBI]
|
4.22647e-05
|
|
|
SLC12A1
|
[NCBI]
|
4.01011e-05
|
|
|
HHRH
|
[NCBI]
|
3.95028e-05
|
|
|
alport syndrome, autosomal recessive
|
[NCBI]
|
3.80783e-05
|
|
|
DNASE1
|
[NCBI]
|
3.7608e-05
|
|
|
ACTN4
|
[NCBI]
|
3.7608e-05
|
|
|
sialuria
|
[NCBI]
|
3.67772e-05
|
|
|
BFH
|
[NCBI]
|
3.67772e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
3.66587e-05
|
|
|
NPHS2
|
[NCBI]
|
3.56251e-05
|
|
|
AMN
|
[NCBI]
|
3.56251e-05
|
|
|
EGFR
|
[NCBI]
|
3.51916e-05
|
|
|
LAMB2
|
[NCBI]
|
3.39792e-05
|
|
|
renal tubular acidosis, distal, autosomal dominant
|
[NCBI]
|
3.34424e-05
|
|
|
PTPRO
|
[NCBI]
|
3.25729e-05
|
|
|
HPSE
|
[NCBI]
|
3.25729e-05
|
|
|
DNM2
|
[NCBI]
|
3.25729e-05
|
|
|
DMC
|
[NCBI]
|
3.24798e-05
|
|
|
LPL
|
[NCBI]
|
3.22358e-05
|
|
|
cirrhosis, familial
|
[NCBI]
|
3.1577e-05
|
|
|
myeloma, multiple
|
[NCBI]
|
3.1577e-05
|
|
|
PTGS1
|
[NCBI]
|
2.92804e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
2.84444e-05
|
|
|
MYO6
|
[NCBI]
|
2.83941e-05
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
2.77585e-05
|
|
|
PGF
|
[NCBI]
|
2.75834e-05
|
|
|
CUBN
|
[NCBI]
|
2.75834e-05
|
|
|
FLT1
|
[NCBI]
|
2.68366e-05
|
|
|
ALMS
|
[NCBI]
|
2.53108e-05
|
|
|
mucopolysaccharidosis type iiia
|
[NCBI]
|
2.47615e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.46369e-05
|
|
|
tay-sachs disease, ab variant
|
[NCBI]
|
2.43306e-05
|
|
|
PTPRC
|
[NCBI]
|
2.37967e-05
|
|
|
udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase
|
[NCBI]
|
2.37967e-05
|
|
|
NOS2A
|
[NCBI]
|
2.37967e-05
|
|
|
GAPDH
|
[NCBI]
|
2.35932e-05
|
|
|
RBP4
|
[NCBI]
|
2.28133e-05
|
|
|
PEPD
|
[NCBI]
|
2.28133e-05
|
|
|
PLG
|
[NCBI]
|
2.25977e-05
|
|
|
CTSL
|
[NCBI]
|
2.23584e-05
|
|
|
EDN1
|
[NCBI]
|
2.19251e-05
|
|
|
PAX2
|
[NCBI]
|
2.19251e-05
|
|
|
ENPEP
|
[NCBI]
|
2.03729e-05
|
|
|
EPO
|
[NCBI]
|
2.03652e-05
|
|
|
CST3
|
[NCBI]
|
1.96868e-05
|
|
|
TLR3
|
[NCBI]
|
1.93626e-05
|
|
|
TFPI
|
[NCBI]
|
1.90029e-05
|
|
|
XDH
|
[NCBI]
|
1.85601e-05
|
|
|
GC
|
[NCBI]
|
1.81731e-05
|
|
|
C3
|
[NCBI]
|
1.78993e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
1.59754e-05
|
|
|
CP
|
[NCBI]
|
1.53016e-05
|
|
|
MMP9
|
[NCBI]
|
1.49629e-05
|
|
|
LCN2
|
[NCBI]
|
1.47745e-05
|
|
|
TNFRSF1A
|
[NCBI]
|
1.44101e-05
|
|
|
FGF2
|
[NCBI]
|
1.42338e-05
|
|
|
GPT
|
[NCBI]
|
1.38923e-05
|
|
|
APOE
|
[NCBI]
|
1.378e-05
|
|
|
GRA
|
[NCBI]
|
1.32474e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
1.30974e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
1.24529e-05
|
|
|
PTGS2
|
[NCBI]
|
1.22388e-05
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
1.17153e-05
|
|
|
IDUA
|
[NCBI]
|
1.15898e-05
|
|
|
LPI
|
[NCBI]
|
1.0689e-05
|
|
|
MCP
|
[NCBI]
|
1.03345e-05
|
|
|
GCK
|
[NCBI]
|
1.03345e-05
|
|
|
HP
|
[NCBI]
|
1.03068e-05
|
|
|
PLTP
|
[NCBI]
|
8.42203e-06
|
|
|
RA
|
[NCBI]
|
6.63293e-06
|
|
|
AGER
|
[NCBI]
|
6.465e-06
|
|
|
MAS
|
[NCBI]
|
5.58168e-06
|
|
|
PEDF
|
[NCBI]
|
5.23479e-06
|
|
|
AKR1B1
|
[NCBI]
|
5.05538e-06
|
|
|
NPPA
|
[NCBI]
|
4.50162e-06
|
|
|
CFTR
|
[NCBI]
|
3.475e-06
|
|
|
polycystic kidneys
|
[NCBI]
|
3.44589e-06
|
|
|
INS
|
[NCBI]
|
3.29249e-06
|
|
|
AVP
|
[NCBI]
|
2.96312e-06
|
|
|
EGF
|
[NCBI]
|
2.89529e-06
|
|
|
F3
|
[NCBI]
|
2.63984e-06
|
|
|
AFP
|
[NCBI]
|
2.499e-06
|
|
|
G6PD
|
[NCBI]
|
2.49563e-06
|
|
|
MBL2
|
[NCBI]
|
2.46444e-06
|
|
|
PTH
|
[NCBI]
|
2.01544e-06
|
|
|
PF4
|
[NCBI]
|
7.43487e-07
|
|
|
SOD2
|
[NCBI]
|
5.27856e-07
|
|
|
FRAP1
|
[NCBI]
|
4.26689e-07
|
|
|
TNF
|
[NCBI]
|
3.09068e-07
|
|
|
MPO
|
[NCBI]
|
7.77238e-08
|
|
|
TTR
|
[NCBI]
|
4.06463e-08
|
|
|
HGF
|
[NCBI]
|
2.81201e-08
|
|
|
APOB
|
[NCBI]
|
1.89288e-08
|
|
|
PTHLH
|
[NCBI]
|
1.29575e-08
|
|
|
PPARA
|
[NCBI]
|
1.28285e-08
|
|
|
BWS
|
[NCBI]
|
2.87683e-11
|
|
|
amyloidosis vi
|
[NCBI]
|
1.36132e-11
|
|