|
OMIM |
Link |
Information gain |
01 |
|
ACHE
|
[NCBI]
|
0.0052221
|
|
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.00133596
|
|
|
red skin pigment anomaly of new guinea
|
[NCBI]
|
0.0011398
|
|
|
myopathy, distal, with onset in infancy
|
[NCBI]
|
0.0011398
|
|
|
CHAT
|
[NCBI]
|
0.0010928
|
|
|
myopathy, hyaline body, autosomal recessive
|
[NCBI]
|
0.000875062
|
|
|
spondylodysplasia with pure brachyolmia
|
[NCBI]
|
0.000875062
|
|
|
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers
|
[NCBI]
|
0.00077544
|
|
|
gangliosidosis, gm2, type iii, or juvenile type
|
[NCBI]
|
0.00077544
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.000710915
|
|
|
CEACAM5
|
[NCBI]
|
0.000667978
|
|
|
myopathy, tubular aggregate
|
[NCBI]
|
0.000663058
|
|
|
HLP
|
[NCBI]
|
0.000663058
|
|
|
CDAN3
|
[NCBI]
|
0.000625019
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.000566527
|
|
|
WDM
|
[NCBI]
|
0.000503535
|
|
|
DYT2
|
[NCBI]
|
0.000486602
|
|
|
GFAP
|
[NCBI]
|
0.000484621
|
|
|
IBGC1
|
[NCBI]
|
0.000471124
|
|
|
TH
|
[NCBI]
|
0.000419016
|
|
|
IGAN1
|
[NCBI]
|
0.000409146
|
|
|
small cell cancer of the lung
|
[NCBI]
|
0.000389406
|
|
|
glycogen storage disease ii
|
[NCBI]
|
0.000383824
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.00038032
|
|
|
ACP5
|
[NCBI]
|
0.000374252
|
|
|
hashimoto thyroiditis
|
[NCBI]
|
0.000363476
|
|
|
glycogen storage disease iv
|
[NCBI]
|
0.000331104
|
|
|
CHS
|
[NCBI]
|
0.000308787
|
|
|
MUC1
|
[NCBI]
|
0.000303904
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
0.00025839
|
|
|
TNF
|
[NCBI]
|
0.000253185
|
|
|
KSS
|
[NCBI]
|
0.000239401
|
|
|
VEGF
|
[NCBI]
|
0.000229499
|
|
|
SLE
|
[NCBI]
|
0.00022913
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
0.000226908
|
|
|
G6PD
|
[NCBI]
|
0.000210824
|
|
|
gm1-gangliosidosis, type ii
|
[NCBI]
|
0.000203867
|
|
|
myeloperoxidase deficiency
|
[NCBI]
|
0.000197207
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
0.000192681
|
|
|
CLN3
|
[NCBI]
|
0.000185534
|
|
|
CF
|
[NCBI]
|
0.000169694
|
|
|
ENPEP
|
[NCBI]
|
0.000166929
|
|
|
CLN2
|
[NCBI]
|
0.00016102
|
|
|
cystinosis, adult nonnephropathic
|
[NCBI]
|
0.000149874
|
|
|
central core disease of muscle
|
[NCBI]
|
0.000143801
|
|
|
NPY
|
[NCBI]
|
0.000140983
|
|
|
peroxidase and phospholipid deficiency in eosinophils
|
[NCBI]
|
0.000140866
|
|
|
corneal dystrophy, epithelial basement membrane
|
[NCBI]
|
0.000140866
|
|
|
wolman disease
|
[NCBI]
|
0.000133896
|
|
|
EGFR
|
[NCBI]
|
0.000127481
|
|
|
mitochondrial myopathy
|
[NCBI]
|
0.000122135
|
|
|
mucolipidosis ii
|
[NCBI]
|
0.000118466
|
|
|
CDL1
|
[NCBI]
|
0.000113334
|
|
|
myopathy, congenital, with crystalline intranuclear inclusions
|
[NCBI]
|
0.000108481
|
|
|
dystonia with ringbinden
|
[NCBI]
|
0.000108481
|
|
|
myopathy with storage of glycoproteins and glycosaminoglycans
|
[NCBI]
|
0.000108481
|
|
|
glycoprotein storage disease
|
[NCBI]
|
0.000108481
|
|
|
ovalocytosis, hereditary hemolytic
|
[NCBI]
|
0.000108481
|
|
|
metachromasia of fibroblasts
|
[NCBI]
|
0.000108481
|
|
|
myopathy with abnormal lipid metabolism
|
[NCBI]
|
0.000108481
|
|
|
myotonic myopathy with cylindrical spirals
|
[NCBI]
|
0.000108481
|
|
|
PNMT
|
[NCBI]
|
0.000106
|
|
|
AFP
|
[NCBI]
|
0.000105698
|
|
|
CDS
|
[NCBI]
|
0.00010306
|
|
|
SGD
|
[NCBI]
|
0.00010306
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
0.00010306
|
|
|
MTM1
|
[NCBI]
|
9.90964e-05
|
|
|
NPC1
|
[NCBI]
|
9.69833e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
8.93155e-05
|
|
|
PMC
|
[NCBI]
|
8.83673e-05
|
|
|
GAL
|
[NCBI]
|
8.6888e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
8.63992e-05
|
|
|
mucolipidosis iv
|
[NCBI]
|
8.45316e-05
|
|
|
CLN1
|
[NCBI]
|
8.27552e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
8.27552e-05
|
|
|
glycogen storage disease v
|
[NCBI]
|
8.10619e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
8.10619e-05
|
|
|
VIP
|
[NCBI]
|
8.10481e-05
|
|
|
pleoconial myopathy with salt craving
|
[NCBI]
|
8.07964e-05
|
|
|
myopathy with giant abnormal mitochondria
|
[NCBI]
|
8.07964e-05
|
|
|
hypermetabolism due to defect in mitochondria
|
[NCBI]
|
8.07964e-05
|
|
|
corneal dystrophy, juvenile epithelial, of meesmann
|
[NCBI]
|
8.07964e-05
|
|
|
neuronal intranuclear inclusion disease
|
[NCBI]
|
8.07964e-05
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
8.07964e-05
|
|
|
ACPP
|
[NCBI]
|
7.96852e-05
|
|
|
NEM3
|
[NCBI]
|
7.94445e-05
|
|
|
myoclonic epilepsy of lafora
|
[NCBI]
|
7.49895e-05
|
|
|
RA
|
[NCBI]
|
7.229e-05
|
|
|
LIMM
|
[NCBI]
|
7.04025e-05
|
|
|
AR
|
[NCBI]
|
7.01392e-05
|
|
|
fabry disease
|
[NCBI]
|
6.98333e-05
|
|
|
glycogen storage disease vii
|
[NCBI]
|
6.86241e-05
|
|
|
EGF
|
[NCBI]
|
6.503e-05
|
|
|
OPMD
|
[NCBI]
|
6.48108e-05
|
|
|
amyloidosis, familial visceral
|
[NCBI]
|
6.3684e-05
|
|
|
thyroid hormonogenesis, genetic defect in, 5
|
[NCBI]
|
6.3684e-05
|
|
|
corpus callosum, partial agenesis of, x-linked
|
[NCBI]
|
6.3684e-05
|
|
|
corneal fleck dystrophy
|
[NCBI]
|
6.3684e-05
|
|
|
EPO
|
[NCBI]
|
5.9927e-05
|
|
|
HGF
|
[NCBI]
|
5.92193e-05
|
|
|
APBD
|
[NCBI]
|
5.8711e-05
|
|
|
CSCD
|
[NCBI]
|
5.8711e-05
|
|
|
schindler disease, type i
|
[NCBI]
|
5.8711e-05
|
|
|
NN
|
[NCBI]
|
5.8711e-05
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
5.8711e-05
|
|
|
eunuchoidism, familial hypogonadotropic
|
[NCBI]
|
5.8711e-05
|
|
|
thyrotropin deficiency, isolated
|
[NCBI]
|
5.47662e-05
|
|
|
creatine phosphokinase, elevated serum
|
[NCBI]
|
5.47662e-05
|
|
|
mitochondrial complex iii deficiency
|
[NCBI]
|
5.47662e-05
|
|
|
PPNAD1
|
[NCBI]
|
5.47662e-05
|
|
|
CRH
|
[NCBI]
|
5.4738e-05
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
5.45524e-05
|
|
|
mitochondrial myopathy with diabetes
|
[NCBI]
|
5.15007e-05
|
|
|
EAD
|
[NCBI]
|
5.15007e-05
|
|
|
sulfocysteinuria
|
[NCBI]
|
5.15007e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
5.15007e-05
|
|
|
PMD
|
[NCBI]
|
4.94825e-05
|
|
|
mast cell disease
|
[NCBI]
|
4.8718e-05
|
|
|
myopathy, myosin storage
|
[NCBI]
|
4.8718e-05
|
|
|
BCHE
|
[NCBI]
|
4.77567e-05
|
|
|
INAD1
|
[NCBI]
|
4.62964e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, lethal neonatal
|
[NCBI]
|
4.62964e-05
|
|
|
VDR
|
[NCBI]
|
4.43414e-05
|
|
|
NETH
|
[NCBI]
|
4.41549e-05
|
|
|
corneal dystrophy, gelatinous drop-like
|
[NCBI]
|
4.41549e-05
|
|
|
gaucher disease, perinatal lethal
|
[NCBI]
|
4.41549e-05
|
|
|
OMP
|
[NCBI]
|
4.28404e-05
|
|
|
brody myopathy
|
[NCBI]
|
4.22374e-05
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
4.22374e-05
|
|
|
LDHC
|
[NCBI]
|
4.10882e-05
|
|
|
AD
|
[NCBI]
|
4.10187e-05
|
|
|
F3
|
[NCBI]
|
4.08043e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
4.05027e-05
|
|
|
MCDC1
|
[NCBI]
|
4.05027e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
4.05027e-05
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
4.05027e-05
|
|
|
LGMD2H
|
[NCBI]
|
4.05027e-05
|
|
|
tight skin contracture syndrome, lethal
|
[NCBI]
|
4.05027e-05
|
|
|
DFSP
|
[NCBI]
|
4.0163e-05
|
|
|
GNRH1
|
[NCBI]
|
3.96618e-05
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
3.89205e-05
|
|
|
CDGG1
|
[NCBI]
|
3.89205e-05
|
|
|
amyloidosis v
|
[NCBI]
|
3.89205e-05
|
|
|
NCIE1
|
[NCBI]
|
3.89205e-05
|
|
|
APC
|
[NCBI]
|
3.77947e-05
|
|
|
LPG
|
[NCBI]
|
3.74671e-05
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
3.74671e-05
|
|
|
MAG
|
[NCBI]
|
3.73709e-05
|
|
|
PCNA
|
[NCBI]
|
3.67061e-05
|
|
|
GAN1
|
[NCBI]
|
3.61241e-05
|
|
|
CFTD
|
[NCBI]
|
3.61241e-05
|
|
|
hypophosphatasia, adult type
|
[NCBI]
|
3.61241e-05
|
|
|
JH
|
[NCBI]
|
3.61241e-05
|
|
|
danon disease
|
[NCBI]
|
3.61241e-05
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
3.61241e-05
|
|
|
APOE
|
[NCBI]
|
3.54788e-05
|
|
|
KLK3
|
[NCBI]
|
3.47787e-05
|
|
|
MPO
|
[NCBI]
|
3.43365e-05
|
|
|
PHA
|
[NCBI]
|
3.3713e-05
|
|
|
ZS
|
[NCBI]
|
3.30697e-05
|
|
|
DHFR
|
[NCBI]
|
3.2972e-05
|
|
|
TNFSF6
|
[NCBI]
|
3.2972e-05
|
|
|
BDNF
|
[NCBI]
|
3.17151e-05
|
|
|
NPHP1
|
[NCBI]
|
3.15987e-05
|
|
|
OXT
|
[NCBI]
|
3.12381e-05
|
|
|
krabbe disease
|
[NCBI]
|
3.0961e-05
|
|
|
MSS
|
[NCBI]
|
3.0633e-05
|
|
|
PLOSL
|
[NCBI]
|
3.0633e-05
|
|
|
MEN2B
|
[NCBI]
|
3.0633e-05
|
|
|
refsum disease, infantile form
|
[NCBI]
|
3.0633e-05
|
|
|
TYMS
|
[NCBI]
|
3.00567e-05
|
|
|
ALD
|
[NCBI]
|
3.00509e-05
|
|
|
cutis laxa, x-linked
|
[NCBI]
|
2.97201e-05
|
|
|
CCAL2
|
[NCBI]
|
2.97201e-05
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
2.97201e-05
|
|
|
RTD
|
[NCBI]
|
2.88549e-05
|
|
|
POMC
|
[NCBI]
|
2.80619e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
2.80332e-05
|
|
|
TGD
|
[NCBI]
|
2.80332e-05
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
2.72511e-05
|
|
|
LIP
|
[NCBI]
|
2.72511e-05
|
|
|
EFE
|
[NCBI]
|
2.72511e-05
|
|
|
PPARA
|
[NCBI]
|
2.7203e-05
|
|
|
pheochromocytoma
|
[NCBI]
|
2.5793e-05
|
|
|
PI
|
[NCBI]
|
2.558e-05
|
|
|
OKS
|
[NCBI]
|
2.51115e-05
|
|
|
APOB
|
[NCBI]
|
2.50325e-05
|
|
|
apert syndrome
|
[NCBI]
|
2.38322e-05
|
|
|
HBB
|
[NCBI]
|
2.34891e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
2.32305e-05
|
|
|
LSA
|
[NCBI]
|
2.32305e-05
|
|
|
amyloidosis vi
|
[NCBI]
|
2.30925e-05
|
|
|
DDC
|
[NCBI]
|
2.223e-05
|
|
|
gastric cancer
|
[NCBI]
|
2.20947e-05
|
|
|
FLG
|
[NCBI]
|
2.16784e-05
|
|
|
CAT
|
[NCBI]
|
2.16527e-05
|
|
|
HPS
|
[NCBI]
|
2.13962e-05
|
|
|
SJS1
|
[NCBI]
|
2.05398e-05
|
|
|
CDPX2
|
[NCBI]
|
2.05398e-05
|
|
|
MG
|
[NCBI]
|
2.01924e-05
|
|
|
NGFR
|
[NCBI]
|
1.98347e-05
|
|
|
ATS
|
[NCBI]
|
1.95892e-05
|
|
|
CTNS
|
[NCBI]
|
1.9137e-05
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
1.9137e-05
|
|
|
HHF1
|
[NCBI]
|
1.86989e-05
|
|
|
CDSP
|
[NCBI]
|
1.78628e-05
|
|
|
SHH
|
[NCBI]
|
1.77928e-05
|
|
|
CBY
|
[NCBI]
|
1.75347e-05
|
|
|
MTTA
|
[NCBI]
|
1.75347e-05
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
1.74634e-05
|
|
|
LI1
|
[NCBI]
|
1.70756e-05
|
|
|
JPS
|
[NCBI]
|
1.70756e-05
|
|
|
RBP1
|
[NCBI]
|
1.69825e-05
|
|
|
MTCO3
|
[NCBI]
|
1.67879e-05
|
|
|
ABL
|
[NCBI]
|
1.66989e-05
|
|
|
LAD
|
[NCBI]
|
1.66989e-05
|
|
|
SPARC
|
[NCBI]
|
1.6548e-05
|
|
|
PWS
|
[NCBI]
|
1.64583e-05
|
|
|
COMT
|
[NCBI]
|
1.62039e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.60475e-05
|
|
|
SCA6
|
[NCBI]
|
1.59769e-05
|
|
|
PYY
|
[NCBI]
|
1.56773e-05
|
|
|
CMT1B
|
[NCBI]
|
1.56306e-05
|
|
|
CLIC1
|
[NCBI]
|
1.55603e-05
|
|
|
UTS2
|
[NCBI]
|
1.55603e-05
|
|
|
ADA
|
[NCBI]
|
1.54193e-05
|
|
|
BRRS
|
[NCBI]
|
1.52936e-05
|
|
|
MHS1
|
[NCBI]
|
1.46459e-05
|
|
|
FCMD
|
[NCBI]
|
1.46459e-05
|
|
|
SCA7
|
[NCBI]
|
1.43344e-05
|
|
|
LPL
|
[NCBI]
|
1.41373e-05
|
|
|
LMF1
|
[NCBI]
|
1.41042e-05
|
|
|
DNAJB1
|
[NCBI]
|
1.41042e-05
|
|
|
PIP5K3
|
[NCBI]
|
1.41042e-05
|
|
|
MYH13
|
[NCBI]
|
1.41042e-05
|
|
|
KRT3
|
[NCBI]
|
1.41042e-05
|
|
|
SFRS2
|
[NCBI]
|
1.41042e-05
|
|
|
ST3GAL1
|
[NCBI]
|
1.41042e-05
|
|
|
hurler syndrome
|
[NCBI]
|
1.34461e-05
|
|
|
CJD
|
[NCBI]
|
1.33715e-05
|
|
|
SLS
|
[NCBI]
|
1.31644e-05
|
|
|
NGFB
|
[NCBI]
|
1.31252e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
1.31147e-05
|
|
|
GAPDH
|
[NCBI]
|
1.29959e-05
|
|
|
GSCL
|
[NCBI]
|
1.29535e-05
|
|
|
MPV17
|
[NCBI]
|
1.29535e-05
|
|
|
MAK
|
[NCBI]
|
1.29535e-05
|
|
|
CCBP2
|
[NCBI]
|
1.29535e-05
|
|
|
GCM1
|
[NCBI]
|
1.29535e-05
|
|
|
ST6GAL1
|
[NCBI]
|
1.29535e-05
|
|
|
MAP2
|
[NCBI]
|
1.26175e-05
|
|
|
SOD2
|
[NCBI]
|
1.24928e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
1.24169e-05
|
|
|
GIP
|
[NCBI]
|
1.20728e-05
|
|
|
SLC6A9
|
[NCBI]
|
1.20044e-05
|
|
|
LCP2
|
[NCBI]
|
1.20044e-05
|
|
|
TRIM32
|
[NCBI]
|
1.11988e-05
|
|
|
ENTPD1
|
[NCBI]
|
1.11988e-05
|
|
|
DVL2
|
[NCBI]
|
1.11988e-05
|
|
|
GATA6
|
[NCBI]
|
1.11988e-05
|
|
|
ZBTB32
|
[NCBI]
|
1.11988e-05
|
|
|
MEN2A
|
[NCBI]
|
1.11347e-05
|
|
|
GDNF
|
[NCBI]
|
1.10232e-05
|
|
|
LPI
|
[NCBI]
|
1.09059e-05
|
|
|
metachromatic leukodystrophy
|
[NCBI]
|
1.06822e-05
|
|
|
CNTF
|
[NCBI]
|
1.06125e-05
|
|
|
TK2
|
[NCBI]
|
1.05003e-05
|
|
|
NEUROG3
|
[NCBI]
|
1.05003e-05
|
|
|
MTTE
|
[NCBI]
|
1.05003e-05
|
|
|
RBL1
|
[NCBI]
|
1.05003e-05
|
|
|
menkes disease
|
[NCBI]
|
1.0249e-05
|
|
|
SHBG
|
[NCBI]
|
9.88619e-06
|
|
|
DSC1
|
[NCBI]
|
9.88508e-06
|
|
|
ATP8B1
|
[NCBI]
|
9.88508e-06
|
|
|
PTPRF
|
[NCBI]
|
9.88508e-06
|
|
|
ACVR1
|
[NCBI]
|
9.88508e-06
|
|
|
LEFTY2
|
[NCBI]
|
9.88508e-06
|
|
|
SLC30A3
|
[NCBI]
|
9.88508e-06
|
|
|
SLC18A3
|
[NCBI]
|
9.56856e-06
|
|
|
SI
|
[NCBI]
|
9.56592e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
9.49281e-06
|
|
|
TG
|
[NCBI]
|
9.4366e-06
|
|
|
DAO
|
[NCBI]
|
9.34429e-06
|
|
|
RTN1
|
[NCBI]
|
9.33632e-06
|
|
|
FABP7
|
[NCBI]
|
9.33632e-06
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
9.05419e-06
|
|
|
SMARCA4
|
[NCBI]
|
8.84189e-06
|
|
|
MEIS1
|
[NCBI]
|
8.84189e-06
|
|
|
PITX3
|
[NCBI]
|
8.84189e-06
|
|
|
SMA1
|
[NCBI]
|
8.68763e-06
|
|
|
TFPI2
|
[NCBI]
|
8.65101e-06
|
|
|
ZNF198
|
[NCBI]
|
8.3927e-06
|
|
|
KRT8
|
[NCBI]
|
8.3927e-06
|
|
|
PITX1
|
[NCBI]
|
8.3927e-06
|
|
|
IDH1
|
[NCBI]
|
8.3927e-06
|
|
|
GDF11
|
[NCBI]
|
8.3927e-06
|
|
|
PPY
|
[NCBI]
|
8.3927e-06
|
|
|
SRF
|
[NCBI]
|
8.12116e-06
|
|
|
CGD
|
[NCBI]
|
7.99711e-06
|
|
|
NAGA
|
[NCBI]
|
7.98177e-06
|
|
|
SDHC
|
[NCBI]
|
7.98177e-06
|
|
|
TFF2
|
[NCBI]
|
7.98177e-06
|
|
|
MFS
|
[NCBI]
|
7.93636e-06
|
|
|
SPINK1
|
[NCBI]
|
7.7693e-06
|
|
|
GRP
|
[NCBI]
|
7.72965e-06
|
|
|
MB
|
[NCBI]
|
7.7108e-06
|
|
|
wilson disease
|
[NCBI]
|
7.67172e-06
|
|
|
CGA
|
[NCBI]
|
7.60362e-06
|
|
|
SORBS1
|
[NCBI]
|
7.60362e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
7.47927e-06
|
|
|
MMP13
|
[NCBI]
|
7.25388e-06
|
|
|
HD
|
[NCBI]
|
7.17863e-06
|
|
|
LAMP2
|
[NCBI]
|
6.92897e-06
|
|
|
BAK1
|
[NCBI]
|
6.92897e-06
|
|
|
EN1
|
[NCBI]
|
6.62597e-06
|
|
|
THY1
|
[NCBI]
|
6.62597e-06
|
|
|
PTH
|
[NCBI]
|
6.4849e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
6.36581e-06
|
|
|
P4HB
|
[NCBI]
|
6.34245e-06
|
|
|
PAPPA
|
[NCBI]
|
6.34245e-06
|
|
|
FGF9
|
[NCBI]
|
6.07636e-06
|
|
|
HMOX1
|
[NCBI]
|
6.07636e-06
|
|
|
DBI
|
[NCBI]
|
6.07291e-06
|
|
|
IL3
|
[NCBI]
|
6.07066e-06
|
|
|
CDLS1
|
[NCBI]
|
5.95989e-06
|
|
|
tay-sachs disease, ab variant
|
[NCBI]
|
5.82594e-06
|
|
|
CEACAM6
|
[NCBI]
|
5.82594e-06
|
|
|
BMP2
|
[NCBI]
|
5.641e-06
|
|
|
UGB
|
[NCBI]
|
5.641e-06
|
|
|
NRL
|
[NCBI]
|
5.5897e-06
|
|
|
RNASE3
|
[NCBI]
|
5.51748e-06
|
|
|
PDGFRA
|
[NCBI]
|
5.36635e-06
|
|
|
AMPD1
|
[NCBI]
|
5.36635e-06
|
|
|
SLC5A5
|
[NCBI]
|
5.36635e-06
|
|
|
CYP27B1
|
[NCBI]
|
5.36635e-06
|
|
|
PDGFRB
|
[NCBI]
|
5.36635e-06
|
|
|
NKX2-1
|
[NCBI]
|
5.15477e-06
|
|
|
SLC5A7
|
[NCBI]
|
5.15477e-06
|
|
|
OSM
|
[NCBI]
|
5.03462e-06
|
|
|
MAPK8
|
[NCBI]
|
4.95398e-06
|
|
|
MAP2K1
|
[NCBI]
|
4.95398e-06
|
|
|
SLC17A6
|
[NCBI]
|
4.95398e-06
|
|
|
SDC2
|
[NCBI]
|
4.94911e-06
|
|
|
TGM1
|
[NCBI]
|
4.76312e-06
|
|
|
CCK
|
[NCBI]
|
4.71325e-06
|
|
|
ABP1
|
[NCBI]
|
4.59699e-06
|
|
|
GJA1
|
[NCBI]
|
4.48308e-06
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
4.44135e-06
|
|
|
MLP
|
[NCBI]
|
4.40819e-06
|
|
|
NOS1
|
[NCBI]
|
4.40819e-06
|
|
|
BWS
|
[NCBI]
|
4.20237e-06
|
|
|
PITX2
|
[NCBI]
|
4.08482e-06
|
|
|
CALCA
|
[NCBI]
|
4.08482e-06
|
|
|
INS
|
[NCBI]
|
4.06499e-06
|
|
|
EV
|
[NCBI]
|
4.00597e-06
|
|
|
CHGA
|
[NCBI]
|
3.93365e-06
|
|
|
TTR
|
[NCBI]
|
3.89714e-06
|
|
|
ADH5
|
[NCBI]
|
3.78888e-06
|
|
|
CST3
|
[NCBI]
|
3.78888e-06
|
|
|
HDC
|
[NCBI]
|
3.77462e-06
|
|
|
CTGF
|
[NCBI]
|
3.77028e-06
|
|
|
CP
|
[NCBI]
|
3.71488e-06
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
3.6501e-06
|
|
|
DCN
|
[NCBI]
|
3.6501e-06
|
|
|
COL10A1
|
[NCBI]
|
3.51697e-06
|
|
|
VIM
|
[NCBI]
|
3.48174e-06
|
|
|
MBP
|
[NCBI]
|
3.37459e-06
|
|
|
TF
|
[NCBI]
|
3.24683e-06
|
|
|
PG
|
[NCBI]
|
3.22553e-06
|
|
|
FGF7
|
[NCBI]
|
3.16586e-06
|
|
|
OA1
|
[NCBI]
|
3.1482e-06
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
3.1482e-06
|
|
|
ICAM1
|
[NCBI]
|
3.1482e-06
|
|
|
IL13
|
[NCBI]
|
3.1482e-06
|
|
|
NR6A1
|
[NCBI]
|
3.03456e-06
|
|
|
BAX
|
[NCBI]
|
2.92516e-06
|
|
|
ADRP
|
[NCBI]
|
2.92516e-06
|
|
|
TPI1
|
[NCBI]
|
2.81977e-06
|
|
|
fucosidosis
|
[NCBI]
|
2.62025e-06
|
|
|
RP
|
[NCBI]
|
2.44492e-06
|
|
|
ARF6
|
[NCBI]
|
2.43457e-06
|
|
|
GHR
|
[NCBI]
|
2.40346e-06
|
|
|
CDK2
|
[NCBI]
|
2.37788e-06
|
|
|
HEXB
|
[NCBI]
|
2.34652e-06
|
|
|
BRAF
|
[NCBI]
|
2.34652e-06
|
|
|
RUNX1
|
[NCBI]
|
2.17932e-06
|
|
|
FGFR3
|
[NCBI]
|
2.12643e-06
|
|
|
SERPINA6
|
[NCBI]
|
2.05264e-06
|
|
|
APCS
|
[NCBI]
|
2.02313e-06
|
|
|
HCRT
|
[NCBI]
|
1.87706e-06
|
|
|
COL3A1
|
[NCBI]
|
1.87706e-06
|
|
|
AANAT
|
[NCBI]
|
1.87706e-06
|
|
|
PGR
|
[NCBI]
|
1.74101e-06
|
|
|
XDH
|
[NCBI]
|
1.58471e-06
|
|
|
MYH7
|
[NCBI]
|
1.4922e-06
|
|
|
OTC
|
[NCBI]
|
1.4922e-06
|
|
|
PTHLH
|
[NCBI]
|
1.43619e-06
|
|
|
PLP1
|
[NCBI]
|
1.435e-06
|
|
|
GHRH
|
[NCBI]
|
1.40276e-06
|
|
|
GNRHR
|
[NCBI]
|
1.3796e-06
|
|
|
AKR1B1
|
[NCBI]
|
1.32777e-06
|
|
|
SPP1
|
[NCBI]
|
1.31837e-06
|
|
|
CDH1
|
[NCBI]
|
1.22361e-06
|
|
|
ASL
|
[NCBI]
|
1.22361e-06
|
|
|
MMP9
|
[NCBI]
|
1.22361e-06
|
|
|
TPO
|
[NCBI]
|
1.21336e-06
|
|
|
MMP2
|
[NCBI]
|
1.08179e-06
|
|
|
DNTT
|
[NCBI]
|
1.03744e-06
|
|
|
ADCYAP1
|
[NCBI]
|
1.00383e-06
|
|
|
FOXP3
|
[NCBI]
|
9.94473e-07
|
|
|
PJS
|
[NCBI]
|
9.62326e-07
|
|
|
NMU
|
[NCBI]
|
9.52856e-07
|
|
|
TGFB1
|
[NCBI]
|
9.52856e-07
|
|
|
CD
|
[NCBI]
|
9.1721e-07
|
|
|
GPT
|
[NCBI]
|
9.12544e-07
|
|
|
AVP
|
[NCBI]
|
8.61143e-07
|
|
|
TFF3
|
[NCBI]
|
8.3569e-07
|
|
|
DSPP
|
[NCBI]
|
8.3569e-07
|
|
|
SST
|
[NCBI]
|
7.35355e-07
|
|
|
DGS
|
[NCBI]
|
5.99646e-07
|
|
|
HFE
|
[NCBI]
|
5.85122e-07
|
|
|
DMD
|
[NCBI]
|
5.48913e-07
|
|
|
ACE
|
[NCBI]
|
4.87481e-07
|
|
|
IHH
|
[NCBI]
|
4.5025e-07
|
|
|
BSG
|
[NCBI]
|
4.42236e-07
|
|
|
PF4
|
[NCBI]
|
4.40892e-07
|
|
|
APP
|
[NCBI]
|
4.19712e-07
|
|
|
ASS
|
[NCBI]
|
3.73791e-07
|
|
|
CLU
|
[NCBI]
|
3.73791e-07
|
|
|
PRL
|
[NCBI]
|
3.71192e-07
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
2.57918e-07
|
|
|
FGFR2
|
[NCBI]
|
2.53344e-07
|
|
|
CPI
|
[NCBI]
|
2.32239e-07
|
|
|
TERT
|
[NCBI]
|
1.98734e-07
|
|
|
homocystinuria
|
[NCBI]
|
1.94803e-07
|
|
|
GIST
|
[NCBI]
|
1.89222e-07
|
|
|
CVID
|
[NCBI]
|
1.62408e-07
|
|
|
NPPA
|
[NCBI]
|
1.61144e-07
|
|
|
PAEP
|
[NCBI]
|
1.30207e-07
|
|
|
BL
|
[NCBI]
|
1.28074e-07
|
|
|
PMCH
|
[NCBI]
|
1.11522e-07
|
|
|
TS
|
[NCBI]
|
9.25912e-08
|
|
|
GUSB
|
[NCBI]
|
7.16582e-08
|
|
|
ALB
|
[NCBI]
|
6.70093e-08
|
|
|
AMH
|
[NCBI]
|
5.02591e-08
|
|
|
KDR
|
[NCBI]
|
3.62928e-08
|
|
|
PCI
|
[NCBI]
|
3.16795e-08
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.79598e-08
|
|
|
FGFR1
|
[NCBI]
|
1.58924e-08
|
|
|
MJD
|
[NCBI]
|
1.46989e-08
|
|
|
RNASE2
|
[NCBI]
|
8.35723e-09
|
|
|
UCN
|
[NCBI]
|
3.99549e-09
|
|
|
BCR
|
[NCBI]
|
2.49496e-09
|
|
|
LPO
|
[NCBI]
|
2.42283e-09
|
|
|
PKD1
|
[NCBI]
|
1.24684e-09
|
|
|
GJB1
|
[NCBI]
|
1.24684e-09
|
|
|
UCP2
|
[NCBI]
|
1.24684e-09
|
|
|
CCND1
|
[NCBI]
|
3.84023e-10
|
|