|
OMIM |
Link |
Information gain |
01 |
|
myopathy, autophagic vacuolar, infantile-onset
|
[NCBI]
|
0.00162737
|
|
|
cataract and cardiomyopathy
|
[NCBI]
|
0.00135681
|
|
|
TTR
|
[NCBI]
|
0.00107884
|
|
|
cardiomyopathy associated with myopathy and sudden death
|
[NCBI]
|
0.00102539
|
|
|
noncompaction of left ventricular myocardium, familial isolated, autosomal dominant 2
|
[NCBI]
|
0.00102539
|
|
|
cardiomyopathy, fatal fetal, due to myocardial calcification
|
[NCBI]
|
0.00102539
|
|
|
cardioneuromyopathy with hyaline masses and nemaline rods
|
[NCBI]
|
0.00102539
|
|
|
ARVD1
|
[NCBI]
|
0.000757446
|
|
|
BTHS
|
[NCBI]
|
0.00069241
|
|
|
ARVD3
|
[NCBI]
|
0.000672411
|
|
|
myasthenia, limb-girdle, with tubular aggregates
|
[NCBI]
|
0.000601472
|
|
|
ARVD4
|
[NCBI]
|
0.000601472
|
|
|
fatty metamorphosis of viscera
|
[NCBI]
|
0.000553054
|
|
|
ZLS
|
[NCBI]
|
0.000486675
|
|
|
danon disease
|
[NCBI]
|
0.000484523
|
|
|
CMD1A
|
[NCBI]
|
0.00045652
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
0.000451496
|
|
|
CDSP
|
[NCBI]
|
0.000414688
|
|
|
CMH
|
[NCBI]
|
0.000399775
|
|
|
EDMD2
|
[NCBI]
|
0.000386184
|
|
|
RA
|
[NCBI]
|
0.000385442
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
0.000363486
|
|
|
EFE
|
[NCBI]
|
0.000341903
|
|
|
MVP
|
[NCBI]
|
0.000327984
|
|
|
TAZ
|
[NCBI]
|
0.00032331
|
|
|
NPPA
|
[NCBI]
|
0.000310095
|
|
|
glycogen storage disease of heart, lethal congenital
|
[NCBI]
|
0.000260497
|
|
|
LVNC1
|
[NCBI]
|
0.000242447
|
|
|
DES
|
[NCBI]
|
0.000218603
|
|
|
LAMP2
|
[NCBI]
|
0.000185931
|
|
|
glycogen storage disease ii
|
[NCBI]
|
0.000183515
|
|
|
SGCB
|
[NCBI]
|
0.000181175
|
|
|
BMD
|
[NCBI]
|
0.000175837
|
|
|
acyl-coa dehydrogenase, very long-chain, deficiency of
|
[NCBI]
|
0.000169007
|
|
|
FRDA
|
[NCBI]
|
0.000164435
|
|
|
SLC22A5
|
[NCBI]
|
0.000155783
|
|
|
GACI
|
[NCBI]
|
0.000153273
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
0.000153273
|
|
|
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
|
[NCBI]
|
0.000143427
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
0.000143271
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
0.000135037
|
|
|
cardiomyopathy, familial hypertrophic, with wolff-parkinson-white syndrome
|
[NCBI]
|
0.00013016
|
|
|
acyl-coa dehydrogenase, long-chain, deficiency of
|
[NCBI]
|
0.00013016
|
|
|
MYH7
|
[NCBI]
|
0.000113371
|
|
|
CMD3B
|
[NCBI]
|
0.000107791
|
|
|
muscular dystrophy, cardiac type
|
[NCBI]
|
9.88934e-05
|
|
|
cardioauditory syndrome of sanchez cascos
|
[NCBI]
|
9.88934e-05
|
|
|
ASD4
|
[NCBI]
|
9.88934e-05
|
|
|
uruguay faciocardiomusculoskeletal syndrome
|
[NCBI]
|
9.88934e-05
|
|
|
hypertaurinuric cardiomyopathy
|
[NCBI]
|
9.88934e-05
|
|
|
myotilinopathy
|
[NCBI]
|
9.88934e-05
|
|
|
noncompaction of left ventricular myocardium with congenital heart defects
|
[NCBI]
|
9.88934e-05
|
|
|
cardiac lipidosis, familial
|
[NCBI]
|
9.88934e-05
|
|
|
myopathy, early-onset, with fatal cardiomyopathy
|
[NCBI]
|
9.88934e-05
|
|
|
PDLIM3
|
[NCBI]
|
9.87596e-05
|
|
|
MTTL1
|
[NCBI]
|
9.56735e-05
|
|
|
RYR2
|
[NCBI]
|
9.51444e-05
|
|
|
PLN
|
[NCBI]
|
9.30069e-05
|
|
|
MTTG
|
[NCBI]
|
9.28874e-05
|
|
|
CF
|
[NCBI]
|
8.89623e-05
|
|
|
MTTH
|
[NCBI]
|
8.83913e-05
|
|
|
MLYCD
|
[NCBI]
|
8.47424e-05
|
|
|
APCS
|
[NCBI]
|
8.34557e-05
|
|
|
ALMS
|
[NCBI]
|
8.31989e-05
|
|
|
MB
|
[NCBI]
|
7.97517e-05
|
|
|
PRKAG2
|
[NCBI]
|
7.90166e-05
|
|
|
LCA1
|
[NCBI]
|
7.87019e-05
|
|
|
VEGF
|
[NCBI]
|
7.84987e-05
|
|
|
MTTI
|
[NCBI]
|
7.66813e-05
|
|
|
mitochondrial myopathy with lactic acidosis
|
[NCBI]
|
7.6457e-05
|
|
|
microcephaly-cardiomyopathy
|
[NCBI]
|
7.6457e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
7.47871e-05
|
|
|
fabry disease
|
[NCBI]
|
7.40909e-05
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
7.38832e-05
|
|
|
SGCD
|
[NCBI]
|
7.27126e-05
|
|
|
ACADVL
|
[NCBI]
|
6.94181e-05
|
|
|
cardiogenital syndrome
|
[NCBI]
|
6.80112e-05
|
|
|
ARVD9
|
[NCBI]
|
6.80112e-05
|
|
|
CMD1P
|
[NCBI]
|
6.80112e-05
|
|
|
aneurysm of interventricular septum
|
[NCBI]
|
6.80112e-05
|
|
|
myopathy with storage of glycoproteins and glycosaminoglycans
|
[NCBI]
|
6.80112e-05
|
|
|
CMD1L
|
[NCBI]
|
6.80112e-05
|
|
|
LIMM
|
[NCBI]
|
6.80112e-05
|
|
|
NEM3
|
[NCBI]
|
6.54182e-05
|
|
|
DSP
|
[NCBI]
|
6.5335e-05
|
|
|
SLC25A20
|
[NCBI]
|
6.5335e-05
|
|
|
C14ORF4
|
[NCBI]
|
6.31237e-05
|
|
|
SRFBP1
|
[NCBI]
|
6.31237e-05
|
|
|
cardiomyopathy-hypogonadism-collagenoma syndrome
|
[NCBI]
|
6.25391e-05
|
|
|
atrial standstill
|
[NCBI]
|
6.25391e-05
|
|
|
cardiomyopathy, congestive, with hypergonadotropic hypogonadism
|
[NCBI]
|
6.25391e-05
|
|
|
TTN
|
[NCBI]
|
6.19665e-05
|
|
|
costello syndrome
|
[NCBI]
|
6.10779e-05
|
|
|
HFE
|
[NCBI]
|
5.99152e-05
|
|
|
LMNA
|
[NCBI]
|
5.86829e-05
|
|
|
DFNA10
|
[NCBI]
|
5.84794e-05
|
|
|
SOD2
|
[NCBI]
|
5.81393e-05
|
|
|
ARVD2
|
[NCBI]
|
5.52517e-05
|
|
|
SLE
|
[NCBI]
|
5.51023e-05
|
|
|
DMD
|
[NCBI]
|
5.45579e-05
|
|
|
gaucher disease, type iiic
|
[NCBI]
|
5.02861e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, lethal neonatal
|
[NCBI]
|
5.02861e-05
|
|
|
RCM1
|
[NCBI]
|
5.02861e-05
|
|
|
carnitine palmitoyltransferase i deficiency
|
[NCBI]
|
5.02861e-05
|
|
|
MPD1
|
[NCBI]
|
5.02861e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
4.94521e-05
|
|
|
PTP4A3
|
[NCBI]
|
4.93603e-05
|
|
|
TBX20
|
[NCBI]
|
4.93603e-05
|
|
|
NDUFS2
|
[NCBI]
|
4.93603e-05
|
|
|
LPL
|
[NCBI]
|
4.86974e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 2
|
[NCBI]
|
4.82907e-05
|
|
|
PVOD
|
[NCBI]
|
4.82907e-05
|
|
|
alpha-methylacetoacetic aciduria
|
[NCBI]
|
4.82907e-05
|
|
|
LGMD2E
|
[NCBI]
|
4.65221e-05
|
|
|
d-2-@hydroxyglutaric aciduria
|
[NCBI]
|
4.49346e-05
|
|
|
SSPN
|
[NCBI]
|
4.41762e-05
|
|
|
NDUFV2
|
[NCBI]
|
4.41762e-05
|
|
|
LTBP4
|
[NCBI]
|
4.41762e-05
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
4.34952e-05
|
|
|
NS1
|
[NCBI]
|
4.30706e-05
|
|
|
FXN
|
[NCBI]
|
4.28809e-05
|
|
|
APOA1
|
[NCBI]
|
4.28809e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
4.2179e-05
|
|
|
LGMD1B
|
[NCBI]
|
4.2179e-05
|
|
|
LGMD2D
|
[NCBI]
|
4.2179e-05
|
|
|
HEY2
|
[NCBI]
|
4.08157e-05
|
|
|
PPP1R13L
|
[NCBI]
|
4.08157e-05
|
|
|
MTTL2
|
[NCBI]
|
4.08157e-05
|
|
|
COX15
|
[NCBI]
|
4.08157e-05
|
|
|
DMD
|
[NCBI]
|
3.91286e-05
|
|
|
MAP4
|
[NCBI]
|
3.83213e-05
|
|
|
COX10
|
[NCBI]
|
3.83213e-05
|
|
|
PRKCA
|
[NCBI]
|
3.6337e-05
|
|
|
TRPC6
|
[NCBI]
|
3.6337e-05
|
|
|
TXN
|
[NCBI]
|
3.6337e-05
|
|
|
DTNA
|
[NCBI]
|
3.6337e-05
|
|
|
SLC27A1
|
[NCBI]
|
3.6337e-05
|
|
|
heart block, congenital
|
[NCBI]
|
3.60392e-05
|
|
|
JH
|
[NCBI]
|
3.60392e-05
|
|
|
SRF
|
[NCBI]
|
3.58771e-05
|
|
|
UMS
|
[NCBI]
|
3.52219e-05
|
|
|
TNNI3
|
[NCBI]
|
3.46898e-05
|
|
|
bethlem myopathy
|
[NCBI]
|
3.44474e-05
|
|
|
SCO2
|
[NCBI]
|
3.32822e-05
|
|
|
TTID
|
[NCBI]
|
3.32822e-05
|
|
|
acromegaly
|
[NCBI]
|
3.23419e-05
|
|
|
ALMS1
|
[NCBI]
|
3.20537e-05
|
|
|
COL6A3
|
[NCBI]
|
3.20537e-05
|
|
|
CACNA1C
|
[NCBI]
|
3.20537e-05
|
|
|
PFHB1A
|
[NCBI]
|
3.17026e-05
|
|
|
BSCL2
|
[NCBI]
|
3.09642e-05
|
|
|
SGCG
|
[NCBI]
|
2.99858e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
2.93959e-05
|
|
|
COL6A2
|
[NCBI]
|
2.90982e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
2.8369e-05
|
|
|
HRPT1
|
[NCBI]
|
2.8369e-05
|
|
|
UTRN
|
[NCBI]
|
2.82862e-05
|
|
|
MADD
|
[NCBI]
|
2.78823e-05
|
|
|
ANXA5
|
[NCBI]
|
2.75382e-05
|
|
|
GATA4
|
[NCBI]
|
2.75382e-05
|
|
|
MCOPS7
|
[NCBI]
|
2.74119e-05
|
|
|
HADHA
|
[NCBI]
|
2.68448e-05
|
|
|
SLC6A8
|
[NCBI]
|
2.68448e-05
|
|
|
PPARD
|
[NCBI]
|
2.6199e-05
|
|
|
CAT
|
[NCBI]
|
2.59318e-05
|
|
|
LGMD2A
|
[NCBI]
|
2.56754e-05
|
|
|
NKX2E
|
[NCBI]
|
2.39856e-05
|
|
|
MTCYB
|
[NCBI]
|
2.39856e-05
|
|
|
SPP1
|
[NCBI]
|
2.33726e-05
|
|
|
SLC25A4
|
[NCBI]
|
2.30495e-05
|
|
|
XK
|
[NCBI]
|
2.30495e-05
|
|
|
COL6A1
|
[NCBI]
|
2.21999e-05
|
|
|
TNNT2
|
[NCBI]
|
2.10574e-05
|
|
|
ICAM1
|
[NCBI]
|
2.10574e-05
|
|
|
PCNA
|
[NCBI]
|
2.10188e-05
|
|
|
EDMD
|
[NCBI]
|
2.06389e-05
|
|
|
DM2
|
[NCBI]
|
2.03634e-05
|
|
|
PXE
|
[NCBI]
|
1.99947e-05
|
|
|
DYSF
|
[NCBI]
|
1.97292e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
1.91325e-05
|
|
|
GLB1
|
[NCBI]
|
1.88485e-05
|
|
|
MTRNR1
|
[NCBI]
|
1.88485e-05
|
|
|
AVP
|
[NCBI]
|
1.87554e-05
|
|
|
BRRS
|
[NCBI]
|
1.85886e-05
|
|
|
HOS
|
[NCBI]
|
1.83547e-05
|
|
|
GLA
|
[NCBI]
|
1.83068e-05
|
|
|
CLS
|
[NCBI]
|
1.74621e-05
|
|
|
hurler syndrome
|
[NCBI]
|
1.7249e-05
|
|
|
LQT1
|
[NCBI]
|
1.64334e-05
|
|
|
MPO
|
[NCBI]
|
1.59148e-05
|
|
|
EPO
|
[NCBI]
|
1.59016e-05
|
|
|
CSF3
|
[NCBI]
|
1.56201e-05
|
|
|
HRAS
|
[NCBI]
|
1.56201e-05
|
|
|
AQP2
|
[NCBI]
|
1.54303e-05
|
|
|
BLM
|
[NCBI]
|
1.53089e-05
|
|
|
MTND4
|
[NCBI]
|
1.43749e-05
|
|
|
KRAS
|
[NCBI]
|
1.34408e-05
|
|
|
UCP2
|
[NCBI]
|
1.22183e-05
|
|
|
GBA
|
[NCBI]
|
1.04363e-05
|
|
|
wilson disease
|
[NCBI]
|
1.04059e-05
|
|
|
ACADM
|
[NCBI]
|
1.01456e-05
|
|
|
FBN1
|
[NCBI]
|
8.4673e-06
|
|
|
FRAP1
|
[NCBI]
|
8.2999e-06
|
|
|
TNF
|
[NCBI]
|
7.74429e-06
|
|
|
XDH
|
[NCBI]
|
7.71466e-06
|
|
|
HGF
|
[NCBI]
|
6.9183e-06
|
|
|
KSS
|
[NCBI]
|
6.71003e-06
|
|
|
PTH
|
[NCBI]
|
6.66491e-06
|
|
|
ADM
|
[NCBI]
|
5.56773e-06
|
|
|
GJA1
|
[NCBI]
|
5.17499e-06
|
|
|
DGS
|
[NCBI]
|
4.94224e-06
|
|
|
GPI
|
[NCBI]
|
4.85012e-06
|
|
|
PPARA
|
[NCBI]
|
4.08999e-06
|
|
|
CP
|
[NCBI]
|
3.2534e-06
|
|
|
LDLR
|
[NCBI]
|
3.14733e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
3.13003e-06
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.71686e-06
|
|
|
ACE
|
[NCBI]
|
2.10451e-06
|
|
|
AHR
|
[NCBI]
|
1.62893e-06
|
|
|
CD
|
[NCBI]
|
1.60154e-06
|
|
|
VIP
|
[NCBI]
|
1.54417e-06
|
|
|
NF1
|
[NCBI]
|
1.31568e-06
|
|
|
TNFSF6
|
[NCBI]
|
1.27377e-06
|
|
|
ADA
|
[NCBI]
|
1.04768e-06
|
|
|
CTGF
|
[NCBI]
|
9.82142e-07
|
|
|
TLR4
|
[NCBI]
|
9.60833e-07
|
|
|
RNASE3
|
[NCBI]
|
9.39897e-07
|
|
|
TF
|
[NCBI]
|
7.46485e-07
|
|
|
PTK2
|
[NCBI]
|
1.98233e-07
|
|
|
G6PD
|
[NCBI]
|
1.70939e-07
|
|
|
TH
|
[NCBI]
|
1.36103e-07
|
|
|
APOB
|
[NCBI]
|
6.275e-10
|
|