|
OMIM |
Link |
Information gain |
01 |
|
CMH
|
[NCBI]
|
0.0103978
|
|
|
cataract and cardiomyopathy
|
[NCBI]
|
0.00462338
|
|
|
MYH7
|
[NCBI]
|
0.00168858
|
|
|
CMH4
|
[NCBI]
|
0.000891517
|
|
|
MYBPC3
|
[NCBI]
|
0.000830729
|
|
|
TNNT2
|
[NCBI]
|
0.000792063
|
|
|
CMH3
|
[NCBI]
|
0.000395411
|
|
|
costello syndrome
|
[NCBI]
|
0.000356882
|
|
|
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome
|
[NCBI]
|
0.000318027
|
|
|
TPM1
|
[NCBI]
|
0.000294909
|
|
|
leopard syndrome 1
|
[NCBI]
|
0.000273383
|
|
|
SLE
|
[NCBI]
|
0.000263709
|
|
|
wolff-parkinson-white syndrome
|
[NCBI]
|
0.000249992
|
|
|
danon disease
|
[NCBI]
|
0.000233753
|
|
|
TNNI3
|
[NCBI]
|
0.000230353
|
|
|
CMH10
|
[NCBI]
|
0.000197544
|
|
|
subaortic stenosis--short stature syndrome
|
[NCBI]
|
0.000197544
|
|
|
MYL2
|
[NCBI]
|
0.00017484
|
|
|
FRDA
|
[NCBI]
|
0.000163659
|
|
|
SCO2
|
[NCBI]
|
0.000155707
|
|
|
PRKAG2
|
[NCBI]
|
0.000151381
|
|
|
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
|
[NCBI]
|
0.000143104
|
|
|
EFE
|
[NCBI]
|
0.000134561
|
|
|
RCM1
|
[NCBI]
|
0.000124836
|
|
|
fibromuscular dysplasia of arteries
|
[NCBI]
|
0.000102536
|
|
|
COXPD5
|
[NCBI]
|
9.87317e-05
|
|
|
mitochondrial phosphate carrier deficiency
|
[NCBI]
|
9.87317e-05
|
|
|
leopard syndrome 2
|
[NCBI]
|
9.87317e-05
|
|
|
pulmonic stenosis and deafness
|
[NCBI]
|
9.87317e-05
|
|
|
CMH2
|
[NCBI]
|
9.87317e-05
|
|
|
pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities
|
[NCBI]
|
9.87317e-05
|
|
|
HRAS
|
[NCBI]
|
9.71283e-05
|
|
|
MYH6
|
[NCBI]
|
9.41096e-05
|
|
|
LAMP2
|
[NCBI]
|
8.91044e-05
|
|
|
MTTI
|
[NCBI]
|
8.91044e-05
|
|
|
SGCD
|
[NCBI]
|
8.51196e-05
|
|
|
NS1
|
[NCBI]
|
8.24588e-05
|
|
|
SLC25A20
|
[NCBI]
|
7.77016e-05
|
|
|
subaortic stenosis, membranous
|
[NCBI]
|
7.62957e-05
|
|
|
DFNA22
|
[NCBI]
|
7.62957e-05
|
|
|
glycogen storage disease 0, muscle
|
[NCBI]
|
7.62957e-05
|
|
|
NS5
|
[NCBI]
|
7.62957e-05
|
|
|
mental and growth retardation with amblyopia
|
[NCBI]
|
7.62957e-05
|
|
|
CMH8
|
[NCBI]
|
7.62957e-05
|
|
|
creases, infra-auricular cutaneous, with tall stature and advanced bone age
|
[NCBI]
|
7.62957e-05
|
|
|
CDSP
|
[NCBI]
|
7.54066e-05
|
|
|
TTN
|
[NCBI]
|
7.43087e-05
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
7.35714e-05
|
|
|
LDHCP
|
[NCBI]
|
6.78502e-05
|
|
|
CMD1L
|
[NCBI]
|
6.78502e-05
|
|
|
PLN
|
[NCBI]
|
6.59883e-05
|
|
|
glycogen storage disease of heart, lethal congenital
|
[NCBI]
|
6.23785e-05
|
|
|
glutamate monosodium sensitivity
|
[NCBI]
|
6.23785e-05
|
|
|
alpha-b crystallinopathy
|
[NCBI]
|
6.23785e-05
|
|
|
MEF2C
|
[NCBI]
|
5.5579e-05
|
|
|
SLC25A3
|
[NCBI]
|
5.5579e-05
|
|
|
VCL
|
[NCBI]
|
5.5579e-05
|
|
|
MYOZ2
|
[NCBI]
|
5.5579e-05
|
|
|
TNNC1
|
[NCBI]
|
5.5579e-05
|
|
|
MYL3
|
[NCBI]
|
5.5579e-05
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
5.2414e-05
|
|
|
VDAC1
|
[NCBI]
|
5.03868e-05
|
|
|
NDUFV2
|
[NCBI]
|
5.03868e-05
|
|
|
TNNT3
|
[NCBI]
|
5.03868e-05
|
|
|
HDAC5
|
[NCBI]
|
5.03868e-05
|
|
|
MRPS22
|
[NCBI]
|
5.03868e-05
|
|
|
SVAS
|
[NCBI]
|
4.76805e-05
|
|
|
COX15
|
[NCBI]
|
4.70182e-05
|
|
|
CDK9
|
[NCBI]
|
4.70182e-05
|
|
|
sarcosinemia
|
[NCBI]
|
4.63637e-05
|
|
|
MTTL1
|
[NCBI]
|
4.62791e-05
|
|
|
MTPN
|
[NCBI]
|
4.45157e-05
|
|
|
MTTG
|
[NCBI]
|
4.45157e-05
|
|
|
ACTC1
|
[NCBI]
|
4.08681e-05
|
|
|
NPPB
|
[NCBI]
|
4.08681e-05
|
|
|
GYS1
|
[NCBI]
|
4.08681e-05
|
|
|
MLYCD
|
[NCBI]
|
4.08681e-05
|
|
|
MEF2A
|
[NCBI]
|
3.94523e-05
|
|
|
acyl-coa dehydrogenase, very long-chain, deficiency of
|
[NCBI]
|
3.76659e-05
|
|
|
fabry disease
|
[NCBI]
|
3.71944e-05
|
|
|
RAF1
|
[NCBI]
|
3.71182e-05
|
|
|
MYO6
|
[NCBI]
|
3.5236e-05
|
|
|
ACADVL
|
[NCBI]
|
3.36597e-05
|
|
|
PRKCM
|
[NCBI]
|
3.36597e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
3.2857e-05
|
|
|
infantile sialic acid storage disorder
|
[NCBI]
|
3.03507e-05
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
3.03507e-05
|
|
|
CYP11B2
|
[NCBI]
|
3.00586e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
2.97868e-05
|
|
|
CRYAB
|
[NCBI]
|
2.95706e-05
|
|
|
central core disease of muscle
|
[NCBI]
|
2.92444e-05
|
|
|
PMM2
|
[NCBI]
|
2.78354e-05
|
|
|
AKT1
|
[NCBI]
|
2.70738e-05
|
|
|
MTND1
|
[NCBI]
|
2.67148e-05
|
|
|
CAV3
|
[NCBI]
|
2.63689e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
2.63671e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
2.39877e-05
|
|
|
SLC11A2
|
[NCBI]
|
2.39833e-05
|
|
|
MTATP6
|
[NCBI]
|
2.32259e-05
|
|
|
CMD1A
|
[NCBI]
|
2.29392e-05
|
|
|
BMD
|
[NCBI]
|
2.19681e-05
|
|
|
DMPK
|
[NCBI]
|
2.16687e-05
|
|
|
TNF
|
[NCBI]
|
2.14192e-05
|
|
|
CDG1A
|
[NCBI]
|
2.13588e-05
|
|
|
NOS3
|
[NCBI]
|
2.1075e-05
|
|
|
FXN
|
[NCBI]
|
2.06997e-05
|
|
|
MAP3K5
|
[NCBI]
|
1.93383e-05
|
|
|
FGA
|
[NCBI]
|
1.81583e-05
|
|
|
VEGF
|
[NCBI]
|
1.62687e-05
|
|
|
LMNA
|
[NCBI]
|
1.50634e-05
|
|
|
glycogen storage disease ii
|
[NCBI]
|
1.26458e-05
|
|
|
LS
|
[NCBI]
|
1.25063e-05
|
|
|
WT1
|
[NCBI]
|
1.18363e-05
|
|
|
TTR
|
[NCBI]
|
1.14953e-05
|
|
|
CP
|
[NCBI]
|
7.6659e-06
|
|
|
NPPA
|
[NCBI]
|
6.06969e-06
|
|
|
NF1
|
[NCBI]
|
4.90919e-06
|
|
|
leber optic atrophy
|
[NCBI]
|
4.64023e-06
|
|
|
AFP
|
[NCBI]
|
4.07174e-06
|
|
|
WBS
|
[NCBI]
|
4.01974e-06
|
|
|
HGF
|
[NCBI]
|
7.29236e-07
|
|
|
PCNA
|
[NCBI]
|
4.8652e-07
|
|
|
CAT
|
[NCBI]
|
2.80808e-08
|
|