|
OMIM |
Link |
Information gain |
01 |
|
IGAN1
|
[NCBI]
|
0.00202146
|
|
|
PTH
|
[NCBI]
|
0.0018806
|
|
|
azotemia, familial
|
[NCBI]
|
0.00174151
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.00154489
|
|
|
cryoglobulinemia, familial mixed
|
[NCBI]
|
0.00132303
|
|
|
IBGC1
|
[NCBI]
|
0.0011856
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.00113239
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000915676
|
|
|
SLE
|
[NCBI]
|
0.000854272
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
0.000440694
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000426928
|
|
|
hypouricemia, renal
|
[NCBI]
|
0.000414958
|
|
|
AVP
|
[NCBI]
|
0.000316118
|
|
|
polycystic kidneys
|
[NCBI]
|
0.000307171
|
|
|
NPPA
|
[NCBI]
|
0.000239705
|
|
|
EPO
|
[NCBI]
|
0.000218562
|
|
|
HHC1
|
[NCBI]
|
0.00020935
|
|
|
ALB
|
[NCBI]
|
0.000163504
|
|
|
CAT
|
[NCBI]
|
0.000137009
|
|
|
formiminotransferase deficiency
|
[NCBI]
|
0.000130582
|
|
|
BGLAP
|
[NCBI]
|
0.000125197
|
|
|
CTNS
|
[NCBI]
|
0.000124414
|
|
|
amenorrhea-galactorrhea syndrome
|
[NCBI]
|
0.000124237
|
|
|
ichthyosis, mental retardation, dwarfism, and renal impairment
|
[NCBI]
|
0.000124237
|
|
|
GAMT
|
[NCBI]
|
0.000112304
|
|
|
MPO
|
[NCBI]
|
0.000106234
|
|
|
HNFJ
|
[NCBI]
|
9.02177e-05
|
|
|
ATS
|
[NCBI]
|
8.69032e-05
|
|
|
cystinuria
|
[NCBI]
|
8.38399e-05
|
|
|
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency
|
[NCBI]
|
8.23916e-05
|
|
|
acyl-coa dehydrogenase, medium-chain, deficiency of
|
[NCBI]
|
8.09941e-05
|
|
|
aminoadipic aciduria
|
[NCBI]
|
8.09173e-05
|
|
|
NGFB
|
[NCBI]
|
7.44044e-05
|
|
|
barraquer-simons syndrome
|
[NCBI]
|
7.32717e-05
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
7.32717e-05
|
|
|
membranoproliferative glomerulonephritis, x-linked
|
[NCBI]
|
7.32717e-05
|
|
|
FSGS1
|
[NCBI]
|
6.76116e-05
|
|
|
hypophosphatemic rickets, x-linked dominant
|
[NCBI]
|
6.62961e-05
|
|
|
TRS
|
[NCBI]
|
6.31208e-05
|
|
|
hyperostosis corticalis generalisata, benign form of worth, with torus palatinus
|
[NCBI]
|
5.94028e-05
|
|
|
bartter syndrome, infantile, with sensorineural deafness
|
[NCBI]
|
5.94028e-05
|
|
|
CRC
|
[NCBI]
|
5.8953e-05
|
|
|
amyloidosis, familial visceral
|
[NCBI]
|
5.62339e-05
|
|
|
creatine deficiency syndrome, x-linked
|
[NCBI]
|
5.62339e-05
|
|
|
renal tubular acidosis, distal, autosomal dominant
|
[NCBI]
|
5.34757e-05
|
|
|
renal cysts and diabetes syndrome
|
[NCBI]
|
5.10362e-05
|
|
|
myeloma, multiple
|
[NCBI]
|
5.10362e-05
|
|
|
HCA2
|
[NCBI]
|
5.10362e-05
|
|
|
AQP2
|
[NCBI]
|
4.30525e-05
|
|
|
LPI
|
[NCBI]
|
4.20872e-05
|
|
|
bartter syndrome, antenatal, type 2
|
[NCBI]
|
4.04604e-05
|
|
|
glutathione synthetase deficiency
|
[NCBI]
|
4.04604e-05
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
4.04604e-05
|
|
|
NPHP1
|
[NCBI]
|
4.04604e-05
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
3.9133e-05
|
|
|
AD
|
[NCBI]
|
3.8287e-05
|
|
|
EGFR
|
[NCBI]
|
3.80052e-05
|
|
|
PDB
|
[NCBI]
|
3.78895e-05
|
|
|
HRPT1
|
[NCBI]
|
3.78895e-05
|
|
|
methionine adenosyltransferase deficiency
|
[NCBI]
|
3.78895e-05
|
|
|
CRH
|
[NCBI]
|
3.68481e-05
|
|
|
PHA2
|
[NCBI]
|
3.67207e-05
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
3.67207e-05
|
|
|
PRL
|
[NCBI]
|
3.60623e-05
|
|
|
lecithin:cholesterol acyltransferase deficiency
|
[NCBI]
|
3.0905e-05
|
|
|
HSAN3
|
[NCBI]
|
2.85657e-05
|
|
|
LCN2
|
[NCBI]
|
2.82374e-05
|
|
|
bartter syndrome, type 3
|
[NCBI]
|
2.78495e-05
|
|
|
CEACAM5
|
[NCBI]
|
2.66782e-05
|
|
|
FIH
|
[NCBI]
|
2.64994e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
2.52475e-05
|
|
|
homocysteinemia
|
[NCBI]
|
2.46547e-05
|
|
|
ACP5
|
[NCBI]
|
2.41204e-05
|
|
|
SPINK1
|
[NCBI]
|
2.36162e-05
|
|
|
ACE
|
[NCBI]
|
2.24589e-05
|
|
|
MBP
|
[NCBI]
|
2.21918e-05
|
|
|
APOE
|
[NCBI]
|
2.2166e-05
|
|
|
aHUS
|
[NCBI]
|
2.19734e-05
|
|
|
MDD
|
[NCBI]
|
2.16901e-05
|
|
|
PHEX
|
[NCBI]
|
2.16497e-05
|
|
|
DJS
|
[NCBI]
|
2.10149e-05
|
|
|
NPS
|
[NCBI]
|
2.05568e-05
|
|
|
ADIPOQ
|
[NCBI]
|
2.03661e-05
|
|
|
CDG1A
|
[NCBI]
|
1.96799e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
1.96799e-05
|
|
|
CTGF
|
[NCBI]
|
1.92756e-05
|
|
|
PG
|
[NCBI]
|
1.92252e-05
|
|
|
biotinidase deficiency
|
[NCBI]
|
1.88511e-05
|
|
|
SMS
|
[NCBI]
|
1.81944e-05
|
|
|
COQ2
|
[NCBI]
|
1.81944e-05
|
|
|
TNF
|
[NCBI]
|
1.74616e-05
|
|
|
HGF
|
[NCBI]
|
1.7192e-05
|
|
|
FGF23
|
[NCBI]
|
1.71461e-05
|
|
|
SLC22A12
|
[NCBI]
|
1.7131e-05
|
|
|
NPY
|
[NCBI]
|
1.55619e-05
|
|
|
PTGIR
|
[NCBI]
|
1.54964e-05
|
|
|
AUH
|
[NCBI]
|
1.54964e-05
|
|
|
ADM
|
[NCBI]
|
1.53927e-05
|
|
|
ENTPD1
|
[NCBI]
|
1.48401e-05
|
|
|
GRHPR
|
[NCBI]
|
1.48401e-05
|
|
|
HGPS
|
[NCBI]
|
1.46909e-05
|
|
|
B2M
|
[NCBI]
|
1.41479e-05
|
|
|
PON2
|
[NCBI]
|
1.32646e-05
|
|
|
SLC7A9
|
[NCBI]
|
1.28327e-05
|
|
|
GUCA2B
|
[NCBI]
|
1.28327e-05
|
|
|
RA
|
[NCBI]
|
1.25464e-05
|
|
|
CYP3A5
|
[NCBI]
|
1.24352e-05
|
|
|
PF4
|
[NCBI]
|
1.22406e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
1.20154e-05
|
|
|
maple syrup urine disease
|
[NCBI]
|
1.20154e-05
|
|
|
COL18A1
|
[NCBI]
|
1.14048e-05
|
|
|
BBS
|
[NCBI]
|
1.13181e-05
|
|
|
SLC22A8
|
[NCBI]
|
1.05545e-05
|
|
|
SLC6A8
|
[NCBI]
|
1.03015e-05
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
9.65161e-06
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
9.65161e-06
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
9.40624e-06
|
|
|
MAP2K1
|
[NCBI]
|
9.20683e-06
|
|
|
SLC3A1
|
[NCBI]
|
9.20683e-06
|
|
|
DHFR
|
[NCBI]
|
8.70571e-06
|
|
|
TNNT2
|
[NCBI]
|
8.65571e-06
|
|
|
VDR
|
[NCBI]
|
8.46213e-06
|
|
|
SLC22A6
|
[NCBI]
|
8.16427e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
7.94094e-06
|
|
|
krabbe disease
|
[NCBI]
|
7.89805e-06
|
|
|
CYP11B2
|
[NCBI]
|
7.72163e-06
|
|
|
GCDH
|
[NCBI]
|
7.58346e-06
|
|
|
G6PD
|
[NCBI]
|
7.42299e-06
|
|
|
PTX3
|
[NCBI]
|
7.31965e-06
|
|
|
PTHLH
|
[NCBI]
|
7.12777e-06
|
|
|
KAL1
|
[NCBI]
|
7.07109e-06
|
|
|
MAS
|
[NCBI]
|
6.84861e-06
|
|
|
VEGF
|
[NCBI]
|
6.7326e-06
|
|
|
TACR1
|
[NCBI]
|
6.72363e-06
|
|
|
coproporphyria
|
[NCBI]
|
6.72363e-06
|
|
|
TNFRSF1B
|
[NCBI]
|
6.72363e-06
|
|
|
ZS
|
[NCBI]
|
6.57211e-06
|
|
|
INS
|
[NCBI]
|
6.53898e-06
|
|
|
EGF
|
[NCBI]
|
6.5106e-06
|
|
|
F3
|
[NCBI]
|
6.24076e-06
|
|
|
FMF
|
[NCBI]
|
6.21012e-06
|
|
|
AGT
|
[NCBI]
|
5.82868e-06
|
|
|
CP
|
[NCBI]
|
5.50191e-06
|
|
|
KLK3
|
[NCBI]
|
5.48924e-06
|
|
|
ALAD
|
[NCBI]
|
5.48752e-06
|
|
|
DAO
|
[NCBI]
|
5.17425e-06
|
|
|
ABP1
|
[NCBI]
|
4.72588e-06
|
|
|
GDNF
|
[NCBI]
|
4.42763e-06
|
|
|
HBB
|
[NCBI]
|
4.31101e-06
|
|
|
REG3A
|
[NCBI]
|
4.08093e-06
|
|
|
PXE
|
[NCBI]
|
3.73134e-06
|
|
|
MTR
|
[NCBI]
|
3.52488e-06
|
|
|
TF
|
[NCBI]
|
3.44279e-06
|
|
|
GPT
|
[NCBI]
|
3.43356e-06
|
|
|
MEN1
|
[NCBI]
|
3.38892e-06
|
|
|
HLA-A
|
[NCBI]
|
3.34492e-06
|
|
|
AQP1
|
[NCBI]
|
3.17521e-06
|
|
|
GAPDH
|
[NCBI]
|
3.17054e-06
|
|
|
PCNA
|
[NCBI]
|
3.03679e-06
|
|
|
TG
|
[NCBI]
|
2.98686e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
2.83404e-06
|
|
|
PTGS2
|
[NCBI]
|
2.71962e-06
|
|
|
CPB2
|
[NCBI]
|
2.5834e-06
|
|
|
CNTF
|
[NCBI]
|
2.52528e-06
|
|
|
TTR
|
[NCBI]
|
2.46635e-06
|
|
|
XDH
|
[NCBI]
|
2.41692e-06
|
|
|
TPMT
|
[NCBI]
|
2.15797e-06
|
|
|
RNASE2
|
[NCBI]
|
1.9459e-06
|
|
|
BWS
|
[NCBI]
|
1.71498e-06
|
|
|
PD
|
[NCBI]
|
1.42602e-06
|
|
|
TFPI
|
[NCBI]
|
1.3937e-06
|
|
|
TYMS
|
[NCBI]
|
1.38336e-06
|
|
|
FGF2
|
[NCBI]
|
1.36068e-06
|
|
|
SPP1
|
[NCBI]
|
1.22204e-06
|
|
|
ACADM
|
[NCBI]
|
9.99675e-07
|
|
|
IL2
|
[NCBI]
|
9.78512e-07
|
|
|
LPL
|
[NCBI]
|
9.72774e-07
|
|
|
SHBG
|
[NCBI]
|
8.97031e-07
|
|
|
LCAT
|
[NCBI]
|
8.76675e-07
|
|
|
TS
|
[NCBI]
|
5.79269e-07
|
|
|
GIP
|
[NCBI]
|
5.33491e-07
|
|
|
ILK
|
[NCBI]
|
4.70977e-07
|
|
|
ALD
|
[NCBI]
|
4.68993e-07
|
|
|
HP
|
[NCBI]
|
3.7648e-07
|
|
|
TNFRSF11B
|
[NCBI]
|
3.2949e-07
|
|
|
COMP
|
[NCBI]
|
2.95048e-07
|
|
|
ABCC1
|
[NCBI]
|
1.92637e-07
|
|
|
MODY
|
[NCBI]
|
1.51918e-07
|
|
|
SOD2
|
[NCBI]
|
9.8729e-08
|
|
|
RTT
|
[NCBI]
|
9.71268e-08
|
|
|
SERPINA6
|
[NCBI]
|
8.58315e-08
|
|
|
SDC2
|
[NCBI]
|
7.99209e-08
|
|
|
COMT
|
[NCBI]
|
6.12323e-08
|
|
|
AFP
|
[NCBI]
|
2.57782e-08
|
|
|
APOB
|
[NCBI]
|
2.49424e-08
|
|
|
PPARA
|
[NCBI]
|
1.85399e-08
|
|
|
IAPP
|
[NCBI]
|
1.54587e-08
|
|
|
FRAP1
|
[NCBI]
|
1.009e-08
|
|
|
STAT3
|
[NCBI]
|
6.72404e-09
|
|
|
CF
|
[NCBI]
|
5.20736e-09
|
|
|
amyloidosis vi
|
[NCBI]
|
1.62039e-09
|
|
|
MBL2
|
[NCBI]
|
1.23062e-09
|
|
|
BCHE
|
[NCBI]
|
1.1256e-10
|
|