|
OMIM |
Link |
Information gain |
01 |
|
diabetes mellitus, transient neonatal, 1
|
[NCBI]
|
0.00105078
|
|
|
muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
|
[NCBI]
|
0.00105062
|
|
|
peripheral arterial occlusive disease 1
|
[NCBI]
|
0.00105062
|
|
|
brachial palsy, familial congenital
|
[NCBI]
|
0.000832846
|
|
|
collagenosis, familial reactive perforating
|
[NCBI]
|
0.000657993
|
|
|
AKR1B1
|
[NCBI]
|
0.000633236
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.000525644
|
|
|
fanconi renotubular syndrome
|
[NCBI]
|
0.000525644
|
|
|
APS2
|
[NCBI]
|
0.00051152
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
0.000347532
|
|
|
diabetes-deafness syndrome, maternally transmitted
|
[NCBI]
|
0.000280096
|
|
|
EKD1
|
[NCBI]
|
0.000248175
|
|
|
WFS1
|
[NCBI]
|
0.000210753
|
|
|
AGER
|
[NCBI]
|
0.00020879
|
|
|
FRDA
|
[NCBI]
|
0.000205566
|
|
|
CF
|
[NCBI]
|
0.000171279
|
|
|
ALMS
|
[NCBI]
|
0.000170254
|
|
|
CGL2
|
[NCBI]
|
0.00016662
|
|
|
MTTE
|
[NCBI]
|
0.00015236
|
|
|
SLC19A2
|
[NCBI]
|
0.000144268
|
|
|
mitochondrial myopathy with diabetes
|
[NCBI]
|
0.000142014
|
|
|
CPAF
|
[NCBI]
|
0.000142014
|
|
|
PNDM
|
[NCBI]
|
0.000121993
|
|
|
HP
|
[NCBI]
|
0.000118405
|
|
|
MTTL1
|
[NCBI]
|
0.000115764
|
|
|
TRMA
|
[NCBI]
|
0.000111534
|
|
|
RA
|
[NCBI]
|
8.95051e-05
|
|
|
MODY8
|
[NCBI]
|
8.48864e-05
|
|
|
hepatic adenomas, familial
|
[NCBI]
|
8.48864e-05
|
|
|
pancreatic beta cell agenesis with neonatal diabetes mellitus
|
[NCBI]
|
8.48864e-05
|
|
|
diabetes mellitus, transient neonatal, 2
|
[NCBI]
|
8.48864e-05
|
|
|
PCTT
|
[NCBI]
|
8.382e-05
|
|
|
stroke, susceptibility to, 1
|
[NCBI]
|
7.64258e-05
|
|
|
arthrogryposis and ectodermal dysplasia
|
[NCBI]
|
7.64258e-05
|
|
|
acrogeria, gottron type
|
[NCBI]
|
7.09389e-05
|
|
|
hairy ears
|
[NCBI]
|
7.09389e-05
|
|
|
tropical calcific pancreatitis
|
[NCBI]
|
6.68645e-05
|
|
|
earlobe crease
|
[NCBI]
|
6.68645e-05
|
|
|
barraquer-simons syndrome
|
[NCBI]
|
6.36219e-05
|
|
|
HOA
|
[NCBI]
|
6.36219e-05
|
|
|
AD
|
[NCBI]
|
5.969e-05
|
|
|
hypertriglyceridemia, familial
|
[NCBI]
|
5.86268e-05
|
|
|
myeloperoxidase deficiency
|
[NCBI]
|
5.66166e-05
|
|
|
AKR1A1
|
[NCBI]
|
5.44706e-05
|
|
|
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities
|
[NCBI]
|
5.17768e-05
|
|
|
renal cysts and diabetes syndrome
|
[NCBI]
|
5.04458e-05
|
|
|
SORD
|
[NCBI]
|
4.92794e-05
|
|
|
CP
|
[NCBI]
|
4.88101e-05
|
|
|
CDS
|
[NCBI]
|
4.80818e-05
|
|
|
kaposi sarcoma
|
[NCBI]
|
4.80818e-05
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
4.60294e-05
|
|
|
CFTD
|
[NCBI]
|
4.60294e-05
|
|
|
KSS
|
[NCBI]
|
4.52067e-05
|
|
|
LPG
|
[NCBI]
|
4.42173e-05
|
|
|
JH
|
[NCBI]
|
4.42173e-05
|
|
|
HYOU1
|
[NCBI]
|
4.34106e-05
|
|
|
SLE
|
[NCBI]
|
4.14491e-05
|
|
|
PON1
|
[NCBI]
|
3.97205e-05
|
|
|
MADA
|
[NCBI]
|
3.91649e-05
|
|
|
KAL2
|
[NCBI]
|
3.85627e-05
|
|
|
PDE4D
|
[NCBI]
|
3.83505e-05
|
|
|
BSCL2
|
[NCBI]
|
3.60185e-05
|
|
|
FCHL
|
[NCBI]
|
3.5383e-05
|
|
|
FPLD2
|
[NCBI]
|
3.49132e-05
|
|
|
LPL
|
[NCBI]
|
3.20426e-05
|
|
|
AIMAH
|
[NCBI]
|
3.19876e-05
|
|
|
SELP
|
[NCBI]
|
3.18642e-05
|
|
|
SPINK1
|
[NCBI]
|
3.17606e-05
|
|
|
IAPP
|
[NCBI]
|
2.98665e-05
|
|
|
HNF1B
|
[NCBI]
|
2.75782e-05
|
|
|
HFE
|
[NCBI]
|
2.66302e-05
|
|
|
KCNJ11
|
[NCBI]
|
2.59928e-05
|
|
|
NIDDM
|
[NCBI]
|
2.59117e-05
|
|
|
APOB
|
[NCBI]
|
2.4713e-05
|
|
|
PWS
|
[NCBI]
|
2.44159e-05
|
|
|
NFKB1
|
[NCBI]
|
2.43262e-05
|
|
|
F3
|
[NCBI]
|
2.37671e-05
|
|
|
CD36
|
[NCBI]
|
2.37349e-05
|
|
|
PTH
|
[NCBI]
|
2.32813e-05
|
|
|
HMGB1
|
[NCBI]
|
2.2655e-05
|
|
|
BLM
|
[NCBI]
|
2.26441e-05
|
|
|
EGF
|
[NCBI]
|
2.00597e-05
|
|
|
EPO
|
[NCBI]
|
1.98345e-05
|
|
|
FXN
|
[NCBI]
|
1.96461e-05
|
|
|
HNF1A
|
[NCBI]
|
1.82935e-05
|
|
|
CEACAM5
|
[NCBI]
|
1.82907e-05
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
1.81382e-05
|
|
|
ABCC8
|
[NCBI]
|
1.79856e-05
|
|
|
PF4
|
[NCBI]
|
1.75286e-05
|
|
|
UCP1
|
[NCBI]
|
1.65914e-05
|
|
|
PNPLA6
|
[NCBI]
|
1.39628e-05
|
|
|
CFH
|
[NCBI]
|
1.37774e-05
|
|
|
INSR
|
[NCBI]
|
1.30764e-05
|
|
|
G6PD
|
[NCBI]
|
1.2118e-05
|
|
|
LEP
|
[NCBI]
|
1.12874e-05
|
|
|
CCK
|
[NCBI]
|
1.04871e-05
|
|
|
PEDF
|
[NCBI]
|
9.79164e-06
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
9.77806e-06
|
|
|
VEGF
|
[NCBI]
|
8.98395e-06
|
|
|
SHBG
|
[NCBI]
|
8.97013e-06
|
|
|
MODY
|
[NCBI]
|
8.65785e-06
|
|
|
TNF
|
[NCBI]
|
8.61771e-06
|
|
|
PYY
|
[NCBI]
|
7.79626e-06
|
|
|
PCNA
|
[NCBI]
|
7.52406e-06
|
|
|
INS
|
[NCBI]
|
7.40888e-06
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
7.22401e-06
|
|
|
PRL
|
[NCBI]
|
6.83648e-06
|
|
|
MJD
|
[NCBI]
|
6.55409e-06
|
|
|
MBL2
|
[NCBI]
|
6.31482e-06
|
|
|
AFP
|
[NCBI]
|
5.54124e-06
|
|
|
MPO
|
[NCBI]
|
5.09587e-06
|
|
|
amyloidosis vi
|
[NCBI]
|
4.63562e-06
|
|
|
GFAP
|
[NCBI]
|
4.55989e-06
|
|
|
PD
|
[NCBI]
|
4.41772e-06
|
|
|
GAPDH
|
[NCBI]
|
4.09651e-06
|
|
|
CTGF
|
[NCBI]
|
3.62671e-06
|
|
|
ALB
|
[NCBI]
|
3.28711e-06
|
|
|
SOD2
|
[NCBI]
|
3.23871e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.28833e-06
|
|
|
APOE
|
[NCBI]
|
1.97037e-06
|
|
|
HGF
|
[NCBI]
|
1.30262e-06
|
|
|
PPARA
|
[NCBI]
|
1.20818e-06
|
|
|
HD
|
[NCBI]
|
6.29016e-07
|
|
|
FA
|
[NCBI]
|
5.05432e-07
|
|
|
CRC
|
[NCBI]
|
4.74886e-07
|
|
|
NPY
|
[NCBI]
|
3.85268e-07
|
|
|
NGFB
|
[NCBI]
|
3.68642e-07
|
|
|
VDR
|
[NCBI]
|
1.75478e-07
|
|
|
CD
|
[NCBI]
|
9.0367e-08
|
|
|
AVP
|
[NCBI]
|
7.55428e-08
|
|