|
OMIM |
Link |
Information gain |
01 |
|
ataxia, deafness, and cardiomyopathy
|
[NCBI]
|
0.00111789
|
|
|
beta-aminoisobutyric acid, urinary excretion of
|
[NCBI]
|
0.000817902
|
|
|
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
|
[NCBI]
|
0.000817902
|
|
|
PFHB1B
|
[NCBI]
|
0.000625244
|
|
|
achalasia, familial esophageal
|
[NCBI]
|
0.000541934
|
|
|
AOS
|
[NCBI]
|
0.000383542
|
|
|
behcet syndrome
|
[NCBI]
|
0.000353076
|
|
|
SLE
|
[NCBI]
|
0.000304596
|
|
|
CMH
|
[NCBI]
|
0.000258317
|
|
|
CMD1A
|
[NCBI]
|
0.000258239
|
|
|
LGMD1B
|
[NCBI]
|
0.000191933
|
|
|
NPPA
|
[NCBI]
|
0.000163257
|
|
|
LQT1
|
[NCBI]
|
0.000160923
|
|
|
IS1
|
[NCBI]
|
0.000149543
|
|
|
cardiomyopathy, dilated, autosomal recessive
|
[NCBI]
|
0.000149093
|
|
|
CF
|
[NCBI]
|
0.000144438
|
|
|
naxos disease
|
[NCBI]
|
0.000126482
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
0.000124206
|
|
|
KSS
|
[NCBI]
|
0.00011167
|
|
|
mowat-wilson syndrome
|
[NCBI]
|
0.000108463
|
|
|
encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts
|
[NCBI]
|
0.000101728
|
|
|
craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation
|
[NCBI]
|
0.000101728
|
|
|
JLNS1
|
[NCBI]
|
9.8701e-05
|
|
|
EDMD2
|
[NCBI]
|
9.5514e-05
|
|
|
SCN5A
|
[NCBI]
|
9.53657e-05
|
|
|
FRDA
|
[NCBI]
|
8.2737e-05
|
|
|
fabry disease
|
[NCBI]
|
8.19623e-05
|
|
|
RA
|
[NCBI]
|
7.87039e-05
|
|
|
LMNA
|
[NCBI]
|
7.73757e-05
|
|
|
HSCR1
|
[NCBI]
|
7.55726e-05
|
|
|
NS4
|
[NCBI]
|
7.08336e-05
|
|
|
MIRN23B
|
[NCBI]
|
6.9573e-05
|
|
|
MIRN199A1
|
[NCBI]
|
6.9573e-05
|
|
|
MIRN214
|
[NCBI]
|
6.9573e-05
|
|
|
MIRN23A
|
[NCBI]
|
6.9573e-05
|
|
|
MIRN208
|
[NCBI]
|
6.9573e-05
|
|
|
WRB
|
[NCBI]
|
6.9573e-05
|
|
|
MIRN195
|
[NCBI]
|
6.9573e-05
|
|
|
KCNA7
|
[NCBI]
|
6.9573e-05
|
|
|
TTR
|
[NCBI]
|
6.7841e-05
|
|
|
RYR2
|
[NCBI]
|
6.78327e-05
|
|
|
EDMD
|
[NCBI]
|
6.76447e-05
|
|
|
hypoascorbemia
|
[NCBI]
|
6.12902e-05
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
5.80566e-05
|
|
|
PPP2CA
|
[NCBI]
|
5.58013e-05
|
|
|
ELK3
|
[NCBI]
|
5.58013e-05
|
|
|
MIRN24-1
|
[NCBI]
|
5.58013e-05
|
|
|
MIRN125B2
|
[NCBI]
|
5.58013e-05
|
|
|
MIRN125B1
|
[NCBI]
|
5.58013e-05
|
|
|
CAT
|
[NCBI]
|
5.56534e-05
|
|
|
young-simpson syndrome
|
[NCBI]
|
5.53726e-05
|
|
|
CMD1E
|
[NCBI]
|
5.53726e-05
|
|
|
sick sinus syndrome, autosomal dominant
|
[NCBI]
|
5.53726e-05
|
|
|
CPVT
|
[NCBI]
|
5.30793e-05
|
|
|
RCM1
|
[NCBI]
|
5.30793e-05
|
|
|
PXE
|
[NCBI]
|
5.29621e-05
|
|
|
glycogen storage disease ii
|
[NCBI]
|
5.00818e-05
|
|
|
IDUA
|
[NCBI]
|
4.95519e-05
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
4.62651e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
4.49431e-05
|
|
|
LGMD2I
|
[NCBI]
|
4.49431e-05
|
|
|
PKP2
|
[NCBI]
|
4.47375e-05
|
|
|
SOS1
|
[NCBI]
|
4.47375e-05
|
|
|
GUSB
|
[NCBI]
|
4.4247e-05
|
|
|
CBR1
|
[NCBI]
|
4.27449e-05
|
|
|
wolff-parkinson-white syndrome
|
[NCBI]
|
4.15458e-05
|
|
|
SLN
|
[NCBI]
|
4.10894e-05
|
|
|
hyperlipoproteinemia, type ii
|
[NCBI]
|
4.05625e-05
|
|
|
hurler-scheie syndrome
|
[NCBI]
|
4.05625e-05
|
|
|
CTGF
|
[NCBI]
|
4.01088e-05
|
|
|
CASQ2
|
[NCBI]
|
3.96735e-05
|
|
|
MYH6
|
[NCBI]
|
3.96735e-05
|
|
|
scheie syndrome
|
[NCBI]
|
3.96388e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
3.96388e-05
|
|
|
CYLD
|
[NCBI]
|
3.96388e-05
|
|
|
TRMA
|
[NCBI]
|
3.87682e-05
|
|
|
ARVD1
|
[NCBI]
|
3.71647e-05
|
|
|
GACI
|
[NCBI]
|
3.57162e-05
|
|
|
HSS
|
[NCBI]
|
3.50417e-05
|
|
|
PFHB1A
|
[NCBI]
|
3.43965e-05
|
|
|
KCNJ2
|
[NCBI]
|
3.38796e-05
|
|
|
ZEB2
|
[NCBI]
|
3.3178e-05
|
|
|
MAPK14
|
[NCBI]
|
3.13352e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
3.10278e-05
|
|
|
HRPT1
|
[NCBI]
|
3.10278e-05
|
|
|
NKX2E
|
[NCBI]
|
3.02773e-05
|
|
|
EMD
|
[NCBI]
|
2.93246e-05
|
|
|
TNF
|
[NCBI]
|
2.92123e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
2.91518e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
2.88816e-05
|
|
|
RBS
|
[NCBI]
|
2.78915e-05
|
|
|
F3
|
[NCBI]
|
2.78286e-05
|
|
|
TNNT2
|
[NCBI]
|
2.7291e-05
|
|
|
FKRP
|
[NCBI]
|
2.69318e-05
|
|
|
BTC
|
[NCBI]
|
2.69318e-05
|
|
|
PLN
|
[NCBI]
|
2.62519e-05
|
|
|
VASP
|
[NCBI]
|
2.56179e-05
|
|
|
ABCC6
|
[NCBI]
|
2.5024e-05
|
|
|
ERBB2
|
[NCBI]
|
2.5024e-05
|
|
|
DES
|
[NCBI]
|
2.44656e-05
|
|
|
GLA
|
[NCBI]
|
2.44656e-05
|
|
|
ACE
|
[NCBI]
|
2.39134e-05
|
|
|
AVP
|
[NCBI]
|
2.32497e-05
|
|
|
CES
|
[NCBI]
|
2.3175e-05
|
|
|
MMP2
|
[NCBI]
|
2.20889e-05
|
|
|
MFS
|
[NCBI]
|
2.20387e-05
|
|
|
aortic valve disease
|
[NCBI]
|
2.13223e-05
|
|
|
MYH7
|
[NCBI]
|
2.09118e-05
|
|
|
APOA1
|
[NCBI]
|
2.09118e-05
|
|
|
GH1
|
[NCBI]
|
2.02044e-05
|
|
|
hurler syndrome
|
[NCBI]
|
1.97034e-05
|
|
|
UCN
|
[NCBI]
|
1.95487e-05
|
|
|
ALGS1
|
[NCBI]
|
1.88643e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
1.88643e-05
|
|
|
RYR1
|
[NCBI]
|
1.8648e-05
|
|
|
TFPI
|
[NCBI]
|
1.75887e-05
|
|
|
TERT
|
[NCBI]
|
1.67339e-05
|
|
|
AVSD
|
[NCBI]
|
1.61534e-05
|
|
|
HHT
|
[NCBI]
|
1.50766e-05
|
|
|
PON1
|
[NCBI]
|
1.46196e-05
|
|
|
AD
|
[NCBI]
|
1.45855e-05
|
|
|
KLK3
|
[NCBI]
|
1.45097e-05
|
|
|
hypercholesterolemia, autosomal dominant
|
[NCBI]
|
1.37e-05
|
|
|
von willebrand disease
|
[NCBI]
|
1.28686e-05
|
|
|
wilson disease
|
[NCBI]
|
1.25972e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
1.23473e-05
|
|
|
LPL
|
[NCBI]
|
1.1238e-05
|
|
|
SHBG
|
[NCBI]
|
1.08344e-05
|
|
|
ADM
|
[NCBI]
|
1.07051e-05
|
|
|
EGFR
|
[NCBI]
|
9.68478e-06
|
|
|
PRNP
|
[NCBI]
|
8.70846e-06
|
|
|
HFE
|
[NCBI]
|
8.51009e-06
|
|
|
VEGF
|
[NCBI]
|
8.0717e-06
|
|
|
TNFSF10
|
[NCBI]
|
7.91319e-06
|
|
|
LDLR
|
[NCBI]
|
7.70303e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
7.60586e-06
|
|
|
MPO
|
[NCBI]
|
7.1394e-06
|
|
|
DGS
|
[NCBI]
|
6.7181e-06
|
|
|
leber optic atrophy
|
[NCBI]
|
6.48676e-06
|
|
|
DMD
|
[NCBI]
|
6.48676e-06
|
|
|
EGF
|
[NCBI]
|
5.82738e-06
|
|
|
PRL
|
[NCBI]
|
5.78079e-06
|
|
|
MDD
|
[NCBI]
|
5.5824e-06
|
|
|
PCNA
|
[NCBI]
|
5.39066e-06
|
|
|
NF1
|
[NCBI]
|
5.06484e-06
|
|
|
GAPDH
|
[NCBI]
|
5.00084e-06
|
|
|
PF4
|
[NCBI]
|
4.53666e-06
|
|
|
TLR4
|
[NCBI]
|
4.46044e-06
|
|
|
ALB
|
[NCBI]
|
4.13267e-06
|
|
|
NGFB
|
[NCBI]
|
3.63933e-06
|
|
|
RTT
|
[NCBI]
|
3.60097e-06
|
|
|
XDH
|
[NCBI]
|
3.55969e-06
|
|
|
EPO
|
[NCBI]
|
3.45591e-06
|
|
|
MJD
|
[NCBI]
|
3.27177e-06
|
|
|
GFAP
|
[NCBI]
|
3.04246e-06
|
|
|
BWS
|
[NCBI]
|
1.86749e-06
|
|
|
APOB
|
[NCBI]
|
1.76023e-06
|
|
|
AS
|
[NCBI]
|
1.57057e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.4999e-06
|
|
|
HD
|
[NCBI]
|
1.10722e-06
|
|
|
MBP
|
[NCBI]
|
7.84443e-07
|
|
|
PD
|
[NCBI]
|
7.56524e-07
|
|
|
VDR
|
[NCBI]
|
4.8087e-07
|
|
|
PTH
|
[NCBI]
|
4.2957e-07
|
|
|
FMF
|
[NCBI]
|
2.5551e-07
|
|
|
TH
|
[NCBI]
|
1.36188e-07
|
|
|
VIP
|
[NCBI]
|
9.19028e-08
|
|
|
MG
|
[NCBI]
|
1.38271e-08
|
|
|
TS
|
[NCBI]
|
4.58473e-11
|
|