|
OMIM |
Link |
Information gain |
01 |
|
PDCD8
|
[NCBI]
|
0.0034675
|
|
|
SOD2
|
[NCBI]
|
0.00178373
|
|
|
leber optic atrophy
|
[NCBI]
|
0.00170457
|
|
|
FRDA
|
[NCBI]
|
0.00145802
|
|
|
medium chain 3-ketoacyl-coa thiolase deficiency
|
[NCBI]
|
0.00131262
|
|
|
myoglobinuria, autosomal dominant
|
[NCBI]
|
0.00131262
|
|
|
GPS
|
[NCBI]
|
0.00103683
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
0.00101218
|
|
|
thyroid hormonogenesis, genetic defect in, 3
|
[NCBI]
|
0.00100225
|
|
|
multiple mitochondrial dysfunctions syndrome
|
[NCBI]
|
0.00100225
|
|
|
necrotizing encephalopathy, acute, autosomal dominant
|
[NCBI]
|
0.00100225
|
|
|
RA
|
[NCBI]
|
0.000934724
|
|
|
LS
|
[NCBI]
|
0.000930555
|
|
|
DFNB15
|
[NCBI]
|
0.000885498
|
|
|
STAR
|
[NCBI]
|
0.000832462
|
|
|
MAFD1
|
[NCBI]
|
0.000818323
|
|
|
OPA4
|
[NCBI]
|
0.000809899
|
|
|
methylmalonic aciduria and homocystinuria, cbld type
|
[NCBI]
|
0.000753845
|
|
|
KSS
|
[NCBI]
|
0.000729501
|
|
|
myopathy with deficiency of succinate dehydrogenase and aconitase
|
[NCBI]
|
0.000672369
|
|
|
CDAN3
|
[NCBI]
|
0.000640841
|
|
|
PARK3
|
[NCBI]
|
0.000640841
|
|
|
myopathy, tubular aggregate
|
[NCBI]
|
0.000640841
|
|
|
parkinson disease, mitochondrial
|
[NCBI]
|
0.000619132
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
0.000609189
|
|
|
storage pool platelet disease
|
[NCBI]
|
0.000589007
|
|
|
OPA1
|
[NCBI]
|
0.000537528
|
|
|
PD
|
[NCBI]
|
0.000525661
|
|
|
alpha-methylacetoacetic aciduria
|
[NCBI]
|
0.000525004
|
|
|
acyl-coa dehydrogenase, very long-chain, deficiency of
|
[NCBI]
|
0.000498798
|
|
|
UCP1
|
[NCBI]
|
0.000483478
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
0.000478704
|
|
|
FXN
|
[NCBI]
|
0.000454561
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.000445089
|
|
|
UCP3
|
[NCBI]
|
0.00042924
|
|
|
UCP2
|
[NCBI]
|
0.000429082
|
|
|
BTHS
|
[NCBI]
|
0.000421187
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
0.00041754
|
|
|
fumarase deficiency
|
[NCBI]
|
0.000404132
|
|
|
CF
|
[NCBI]
|
0.000393698
|
|
|
VEGF
|
[NCBI]
|
0.000369685
|
|
|
mitochondrial myopathy
|
[NCBI]
|
0.000365019
|
|
|
EGF
|
[NCBI]
|
0.00035644
|
|
|
MTND1
|
[NCBI]
|
0.000351913
|
|
|
MELAS
|
[NCBI]
|
0.000337057
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000321336
|
|
|
MTS
|
[NCBI]
|
0.000304101
|
|
|
DNM1L
|
[NCBI]
|
0.000296784
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
0.000295195
|
|
|
MTCYB
|
[NCBI]
|
0.00027481
|
|
|
SLC25A1
|
[NCBI]
|
0.000272783
|
|
|
ACAT1
|
[NCBI]
|
0.000272783
|
|
|
DBI
|
[NCBI]
|
0.000270707
|
|
|
PARK6
|
[NCBI]
|
0.000269669
|
|
|
alzheimer disease, susceptibility to, mitochondrial
|
[NCBI]
|
0.000269669
|
|
|
nephropathy, chronic tubulointerstitial
|
[NCBI]
|
0.000269357
|
|
|
MFN1
|
[NCBI]
|
0.000266226
|
|
|
GPD2
|
[NCBI]
|
0.000266226
|
|
|
PGL1
|
[NCBI]
|
0.000265579
|
|
|
hyperoxaluria, primary, type i
|
[NCBI]
|
0.000253409
|
|
|
MTCO1
|
[NCBI]
|
0.000252316
|
|
|
PINK1
|
[NCBI]
|
0.000251136
|
|
|
GOT2
|
[NCBI]
|
0.000251136
|
|
|
MTRNR1
|
[NCBI]
|
0.000250371
|
|
|
ZS
|
[NCBI]
|
0.000245974
|
|
|
MTCO3
|
[NCBI]
|
0.000244335
|
|
|
MTCO2
|
[NCBI]
|
0.000238802
|
|
|
SLC25A20
|
[NCBI]
|
0.000233692
|
|
|
BAX
|
[NCBI]
|
0.000233305
|
|
|
diabetes-deafness syndrome, maternally transmitted
|
[NCBI]
|
0.000232768
|
|
|
gracile syndrome
|
[NCBI]
|
0.000232768
|
|
|
MTTL1
|
[NCBI]
|
0.00022901
|
|
|
MERRF
|
[NCBI]
|
0.000223469
|
|
|
malonyl-coa decarboxylase deficiency
|
[NCBI]
|
0.0002155
|
|
|
myopathy with giant abnormal mitochondria
|
[NCBI]
|
0.0002155
|
|
|
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|
[NCBI]
|
0.000215142
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
0.000207605
|
|
|
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
[NCBI]
|
0.000207605
|
|
|
ACADM
|
[NCBI]
|
0.000207589
|
|
|
ME2
|
[NCBI]
|
0.000204203
|
|
|
SOD1
|
[NCBI]
|
0.000203809
|
|
|
pearson marrow-pancreas syndrome
|
[NCBI]
|
0.000200724
|
|
|
acyl-coa dehydrogenase, short-chain, deficiency of
|
[NCBI]
|
0.000200724
|
|
|
POLG
|
[NCBI]
|
0.00019672
|
|
|
AVP
|
[NCBI]
|
0.000193276
|
|
|
3-@hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
0.000191292
|
|
|
SPG7
|
[NCBI]
|
0.000191292
|
|
|
DIABLO
|
[NCBI]
|
0.000189648
|
|
|
MTND2
|
[NCBI]
|
0.000186925
|
|
|
BAK1
|
[NCBI]
|
0.000186925
|
|
|
MFN2
|
[NCBI]
|
0.000186241
|
|
|
VDAC1
|
[NCBI]
|
0.000181293
|
|
|
MTATP6
|
[NCBI]
|
0.00017995
|
|
|
OPA1
|
[NCBI]
|
0.000177886
|
|
|
BJS
|
[NCBI]
|
0.000174751
|
|
|
3-@methylcrotonyl-coa carboxylase 1 deficiency
|
[NCBI]
|
0.000174751
|
|
|
pyruvate dehydrogenase phosphatase deficiency
|
[NCBI]
|
0.000174751
|
|
|
MTND3
|
[NCBI]
|
0.000173876
|
|
|
maple syrup urine disease
|
[NCBI]
|
0.000171441
|
|
|
MTND4
|
[NCBI]
|
0.000169035
|
|
|
SLE
|
[NCBI]
|
0.000165161
|
|
|
mitochondrial complex iii deficiency
|
[NCBI]
|
0.000162132
|
|
|
NPY
|
[NCBI]
|
0.00015537
|
|
|
HADHA
|
[NCBI]
|
0.000154608
|
|
|
myopathy, centronuclear, autosomal recessive
|
[NCBI]
|
0.000151928
|
|
|
TRMU
|
[NCBI]
|
0.000146966
|
|
|
ACO2
|
[NCBI]
|
0.000145421
|
|
|
CRH
|
[NCBI]
|
0.00014468
|
|
|
PRL
|
[NCBI]
|
0.000139402
|
|
|
MTND6
|
[NCBI]
|
0.000137667
|
|
|
thalamic degeneration, symmetric infantile
|
[NCBI]
|
0.000134647
|
|
|
25-@hydroxyvitamin d3 deficiency, selective
|
[NCBI]
|
0.000134647
|
|
|
PCH6
|
[NCBI]
|
0.000134647
|
|
|
anemia, congenital sideroblastic, b6-nonresponsive
|
[NCBI]
|
0.000134647
|
|
|
COXPD3
|
[NCBI]
|
0.000134647
|
|
|
hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial
|
[NCBI]
|
0.000134647
|
|
|
mitochondrial intermembrane space protein tim12, yeast, homolog of
|
[NCBI]
|
0.000134647
|
|
|
atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease
|
[NCBI]
|
0.000134647
|
|
|
proximal myopathy with focal depletion of mitochondria
|
[NCBI]
|
0.000134647
|
|
|
PARK13
|
[NCBI]
|
0.000134647
|
|
|
optic atrophy 3, autosomal dominant
|
[NCBI]
|
0.000134647
|
|
|
deafness, autosomal recessive
|
[NCBI]
|
0.000134647
|
|
|
mitochondrial import-stimulating factor
|
[NCBI]
|
0.000134647
|
|
|
hyperlysinemia due to defect in lysine transport into mitochondria
|
[NCBI]
|
0.000134647
|
|
|
TIMM10
|
[NCBI]
|
0.000133084
|
|
|
FTMT
|
[NCBI]
|
0.000133084
|
|
|
SDHD
|
[NCBI]
|
0.000131364
|
|
|
RPS12
|
[NCBI]
|
0.000128463
|
|
|
VDAC2
|
[NCBI]
|
0.000128463
|
|
|
TNFSF10
|
[NCBI]
|
0.000124927
|
|
|
globozoospermia
|
[NCBI]
|
0.000123791
|
|
|
IDH2
|
[NCBI]
|
0.000122123
|
|
|
VIP
|
[NCBI]
|
0.000121347
|
|
|
holocarboxylase synthetase deficiency
|
[NCBI]
|
0.000118619
|
|
|
lipoid congenital adrenal hyperplasia
|
[NCBI]
|
0.000118619
|
|
|
TH
|
[NCBI]
|
0.000118442
|
|
|
BBC3
|
[NCBI]
|
0.000116802
|
|
|
CA5A
|
[NCBI]
|
0.000115136
|
|
|
mas20p, s. cerevisiae, homolog of
|
[NCBI]
|
0.000115136
|
|
|
TXN2
|
[NCBI]
|
0.000115136
|
|
|
propionic acidemia
|
[NCBI]
|
0.00011392
|
|
|
biotinidase deficiency
|
[NCBI]
|
0.00011392
|
|
|
NIDDM
|
[NCBI]
|
0.000113271
|
|
|
SDHC
|
[NCBI]
|
0.000112209
|
|
|
NRF1
|
[NCBI]
|
0.000112209
|
|
|
TIMM8A
|
[NCBI]
|
0.000112209
|
|
|
acyl-coa dehydrogenase, medium-chain, deficiency of
|
[NCBI]
|
0.00010962
|
|
|
MNGIE
|
[NCBI]
|
0.00010962
|
|
|
ACHE
|
[NCBI]
|
0.000109484
|
|
|
SLC25A12
|
[NCBI]
|
0.000105723
|
|
|
NDUFS1
|
[NCBI]
|
0.000105723
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
0.000105658
|
|
|
BID
|
[NCBI]
|
0.000104555
|
|
|
ATP5O
|
[NCBI]
|
0.000104555
|
|
|
MTND4L
|
[NCBI]
|
0.000104555
|
|
|
GOT1
|
[NCBI]
|
0.000101292
|
|
|
CYCS
|
[NCBI]
|
0.000101292
|
|
|
FH
|
[NCBI]
|
9.99211e-05
|
|
|
ATP5J
|
[NCBI]
|
9.98075e-05
|
|
|
CKMT1B
|
[NCBI]
|
9.98075e-05
|
|
|
SLC25A22
|
[NCBI]
|
9.98075e-05
|
|
|
SLC25A14
|
[NCBI]
|
9.98075e-05
|
|
|
PARL
|
[NCBI]
|
9.98075e-05
|
|
|
TIMM8B
|
[NCBI]
|
9.98075e-05
|
|
|
MTHFD1L
|
[NCBI]
|
9.98075e-05
|
|
|
SCO2
|
[NCBI]
|
9.8871e-05
|
|
|
PCK2
|
[NCBI]
|
9.8871e-05
|
|
|
HGF
|
[NCBI]
|
9.58937e-05
|
|
|
pleoconial myopathy with salt craving
|
[NCBI]
|
9.56148e-05
|
|
|
hypermetabolism due to defect in mitochondria
|
[NCBI]
|
9.56148e-05
|
|
|
2-@methylbutyryl-coa dehydrogenase deficiency
|
[NCBI]
|
9.56148e-05
|
|
|
optic atrophy 1 and deafness
|
[NCBI]
|
9.56148e-05
|
|
|
carnitine acetyltransferase deficiency
|
[NCBI]
|
9.56148e-05
|
|
|
longevity
|
[NCBI]
|
9.56148e-05
|
|
|
HHF6
|
[NCBI]
|
9.56148e-05
|
|
|
striatonigral degeneration, infantile, mitochondrial
|
[NCBI]
|
9.56148e-05
|
|
|
MODY
|
[NCBI]
|
9.52778e-05
|
|
|
TFAM
|
[NCBI]
|
9.34342e-05
|
|
|
SDHA
|
[NCBI]
|
9.34342e-05
|
|
|
MPO
|
[NCBI]
|
9.29676e-05
|
|
|
PCNA
|
[NCBI]
|
9.28355e-05
|
|
|
BDNF
|
[NCBI]
|
9.19345e-05
|
|
|
CHAT
|
[NCBI]
|
9.09124e-05
|
|
|
BCL2L1
|
[NCBI]
|
8.89146e-05
|
|
|
CEACAM5
|
[NCBI]
|
8.79754e-05
|
|
|
MAP3K5
|
[NCBI]
|
8.74513e-05
|
|
|
PPID
|
[NCBI]
|
8.64368e-05
|
|
|
MTND5
|
[NCBI]
|
8.64368e-05
|
|
|
PC
|
[NCBI]
|
8.63171e-05
|
|
|
EPO
|
[NCBI]
|
8.62587e-05
|
|
|
MTHFD2
|
[NCBI]
|
8.36797e-05
|
|
|
NDUFV1
|
[NCBI]
|
8.36797e-05
|
|
|
TTC11
|
[NCBI]
|
8.36797e-05
|
|
|
NDUFS7
|
[NCBI]
|
8.36797e-05
|
|
|
TIMM13
|
[NCBI]
|
8.36797e-05
|
|
|
GLRX2
|
[NCBI]
|
8.36797e-05
|
|
|
DAP3
|
[NCBI]
|
8.16563e-05
|
|
|
ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia
|
[NCBI]
|
8.10351e-05
|
|
|
hypotonia-cystinuria syndrome
|
[NCBI]
|
8.10351e-05
|
|
|
retinitis pigmentosa-deafness syndrome
|
[NCBI]
|
8.10351e-05
|
|
|
3-@methylcrotonyl-coa carboxylase 2 deficiency
|
[NCBI]
|
8.10351e-05
|
|
|
PGL3
|
[NCBI]
|
8.10351e-05
|
|
|
DFNA11
|
[NCBI]
|
8.10351e-05
|
|
|
LIMM
|
[NCBI]
|
8.10351e-05
|
|
|
SCP2
|
[NCBI]
|
7.92151e-05
|
|
|
virus-induced signaling adaptor
|
[NCBI]
|
7.86461e-05
|
|
|
PTH
|
[NCBI]
|
7.84419e-05
|
|
|
MTTK
|
[NCBI]
|
7.76945e-05
|
|
|
GAN1
|
[NCBI]
|
7.75321e-05
|
|
|
ACADS
|
[NCBI]
|
7.61937e-05
|
|
|
PPARGC1A
|
[NCBI]
|
7.61937e-05
|
|
|
IDH1
|
[NCBI]
|
7.59377e-05
|
|
|
AGXT
|
[NCBI]
|
7.59377e-05
|
|
|
ENDOG
|
[NCBI]
|
7.5716e-05
|
|
|
SLC25A19
|
[NCBI]
|
7.5716e-05
|
|
|
HTRA2
|
[NCBI]
|
7.5716e-05
|
|
|
NNT
|
[NCBI]
|
7.5716e-05
|
|
|
SLC25A3
|
[NCBI]
|
7.5716e-05
|
|
|
GFM1
|
[NCBI]
|
7.5716e-05
|
|
|
SLC25A15
|
[NCBI]
|
7.5716e-05
|
|
|
NDUFS8
|
[NCBI]
|
7.5716e-05
|
|
|
MBP
|
[NCBI]
|
7.55148e-05
|
|
|
central core disease of muscle
|
[NCBI]
|
7.54625e-05
|
|
|
amyloidosis, familial visceral
|
[NCBI]
|
7.16531e-05
|
|
|
wolfram syndrome, mitochondrial form
|
[NCBI]
|
7.16531e-05
|
|
|
ASAT
|
[NCBI]
|
7.16531e-05
|
|
|
myoclonus and ataxia
|
[NCBI]
|
7.16531e-05
|
|
|
LBSL
|
[NCBI]
|
7.16531e-05
|
|
|
acyl-coa dehydrogenase, long-chain, deficiency of
|
[NCBI]
|
7.16531e-05
|
|
|
hepatitis b virus, susceptibility to
|
[NCBI]
|
7.16531e-05
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
7.16531e-05
|
|
|
DFNA13
|
[NCBI]
|
7.16531e-05
|
|
|
LSFC
|
[NCBI]
|
7.16531e-05
|
|
|
CCK
|
[NCBI]
|
7.15415e-05
|
|
|
AFP
|
[NCBI]
|
7.14724e-05
|
|
|
ABCB7
|
[NCBI]
|
7.00704e-05
|
|
|
SIRT3
|
[NCBI]
|
7.00704e-05
|
|
|
MCOPS7
|
[NCBI]
|
6.97724e-05
|
|
|
SPG7
|
[NCBI]
|
6.91426e-05
|
|
|
HD
|
[NCBI]
|
6.89307e-05
|
|
|
GFAP
|
[NCBI]
|
6.71327e-05
|
|
|
TIMM22
|
[NCBI]
|
6.65347e-05
|
|
|
MRRF
|
[NCBI]
|
6.65347e-05
|
|
|
RARS2
|
[NCBI]
|
6.65347e-05
|
|
|
TFB1M
|
[NCBI]
|
6.65347e-05
|
|
|
SLC25A33
|
[NCBI]
|
6.65347e-05
|
|
|
TIMM9
|
[NCBI]
|
6.65347e-05
|
|
|
MTRF1
|
[NCBI]
|
6.65347e-05
|
|
|
CHCHD4
|
[NCBI]
|
6.65347e-05
|
|
|
PPM1K
|
[NCBI]
|
6.65347e-05
|
|
|
ATP5G2
|
[NCBI]
|
6.65347e-05
|
|
|
TOMM70A
|
[NCBI]
|
6.65347e-05
|
|
|
TOMM22
|
[NCBI]
|
6.65347e-05
|
|
|
ACOT2
|
[NCBI]
|
6.65347e-05
|
|
|
transcription termination factor, mitochondrial
|
[NCBI]
|
6.65347e-05
|
|
|
MRPL12
|
[NCBI]
|
6.65347e-05
|
|
|
CA5B
|
[NCBI]
|
6.65347e-05
|
|
|
NDUFB10
|
[NCBI]
|
6.65347e-05
|
|
|
SLC25A37
|
[NCBI]
|
6.65347e-05
|
|
|
YME1L1
|
[NCBI]
|
6.65347e-05
|
|
|
MTTR
|
[NCBI]
|
6.65347e-05
|
|
|
CKMTS
|
[NCBI]
|
6.65347e-05
|
|
|
ATP5G1
|
[NCBI]
|
6.65347e-05
|
|
|
NDUFA13
|
[NCBI]
|
6.5666e-05
|
|
|
SLC25A11
|
[NCBI]
|
6.5666e-05
|
|
|
ACADVL
|
[NCBI]
|
6.54153e-05
|
|
|
citrullinemia, type ii, neonatal-onset
|
[NCBI]
|
6.47396e-05
|
|
|
adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency
|
[NCBI]
|
6.47396e-05
|
|
|
corticosterone methyloxidase type ii deficiency
|
[NCBI]
|
6.47396e-05
|
|
|
hyperpipecolatemia
|
[NCBI]
|
6.47396e-05
|
|
|
glycogen storage disease 0, muscle
|
[NCBI]
|
6.47396e-05
|
|
|
HNSCC
|
[NCBI]
|
6.47396e-05
|
|
|
dystonia, familial, with visual failure and striatal lucencies
|
[NCBI]
|
6.47396e-05
|
|
|
PBC
|
[NCBI]
|
6.47396e-05
|
|
|
hydroxyacyl-coa dehydrogenase ii deficiency
|
[NCBI]
|
6.47396e-05
|
|
|
AR
|
[NCBI]
|
6.26523e-05
|
|
|
NDUFS4
|
[NCBI]
|
6.20489e-05
|
|
|
MLYCD
|
[NCBI]
|
6.20489e-05
|
|
|
heat-shock protein, 75-kd
|
[NCBI]
|
6.20489e-05
|
|
|
BCS1L
|
[NCBI]
|
6.20489e-05
|
|
|
DFNB7
|
[NCBI]
|
5.92801e-05
|
|
|
IBM3
|
[NCBI]
|
5.92801e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, lethal neonatal
|
[NCBI]
|
5.92801e-05
|
|
|
lactic acidosis, fatal infantile
|
[NCBI]
|
5.92801e-05
|
|
|
deafness, aminoglycoside-induced
|
[NCBI]
|
5.92801e-05
|
|
|
cardiomyopathy, infantile histiocytoid
|
[NCBI]
|
5.92801e-05
|
|
|
AD
|
[NCBI]
|
5.83858e-05
|
|
|
CLN3
|
[NCBI]
|
5.74862e-05
|
|
|
DCK
|
[NCBI]
|
5.74334e-05
|
|
|
MDM1
|
[NCBI]
|
5.63139e-05
|
|
|
PARK2
|
[NCBI]
|
5.53972e-05
|
|
|
CTLN2
|
[NCBI]
|
5.47812e-05
|
|
|
myoclonic epilepsy, neonatal, with suppression-burst pattern
|
[NCBI]
|
5.47812e-05
|
|
|
GLYS1
|
[NCBI]
|
5.47812e-05
|
|
|
DFNA12
|
[NCBI]
|
5.47812e-05
|
|
|
DFFA
|
[NCBI]
|
5.42632e-05
|
|
|
CPT2
|
[NCBI]
|
5.39594e-05
|
|
|
IVD
|
[NCBI]
|
5.39594e-05
|
|
|
HSD17B10
|
[NCBI]
|
5.39594e-05
|
|
|
CFTR
|
[NCBI]
|
5.33141e-05
|
|
|
DFFB
|
[NCBI]
|
5.32069e-05
|
|
|
DARS2
|
[NCBI]
|
5.28541e-05
|
|
|
SCO1
|
[NCBI]
|
5.28541e-05
|
|
|
SIRT4
|
[NCBI]
|
5.28541e-05
|
|
|
mitochondrial ribosomal protein s16: mrps16
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFA8
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFS3
|
[NCBI]
|
5.28541e-05
|
|
|
MTIF2
|
[NCBI]
|
5.28541e-05
|
|
|
SLC25A25
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFB7
|
[NCBI]
|
5.28541e-05
|
|
|
BNIP3L
|
[NCBI]
|
5.28541e-05
|
|
|
UQCRB
|
[NCBI]
|
5.28541e-05
|
|
|
POLRMT
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFAB1
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFA10
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFB9
|
[NCBI]
|
5.28541e-05
|
|
|
TSFM
|
[NCBI]
|
5.28541e-05
|
|
|
ATP5A1
|
[NCBI]
|
5.28541e-05
|
|
|
SLC25A18
|
[NCBI]
|
5.28541e-05
|
|
|
COX17
|
[NCBI]
|
5.28541e-05
|
|
|
NDUFS2
|
[NCBI]
|
5.28541e-05
|
|
|
RPS14
|
[NCBI]
|
5.18519e-05
|
|
|
CVS
|
[NCBI]
|
5.09652e-05
|
|
|
halothane hepatitis
|
[NCBI]
|
5.09652e-05
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
5.09652e-05
|
|
|
OTC
|
[NCBI]
|
5.00987e-05
|
|
|
SCN3
|
[NCBI]
|
4.76597e-05
|
|
|
TRMA
|
[NCBI]
|
4.76597e-05
|
|
|
carnitine palmitoyltransferase i deficiency
|
[NCBI]
|
4.76597e-05
|
|
|
pheochromocytoma
|
[NCBI]
|
4.76597e-05
|
|
|
CDB1
|
[NCBI]
|
4.76597e-05
|
|
|
leiomyomatosis and renal cell cancer, hereditary
|
[NCBI]
|
4.76597e-05
|
|
|
IVA
|
[NCBI]
|
4.76597e-05
|
|
|
CMT2A2
|
[NCBI]
|
4.76597e-05
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
4.76597e-05
|
|
|
MG
|
[NCBI]
|
4.6899e-05
|
|
|
ADA
|
[NCBI]
|
4.675e-05
|
|
|
PRDX3
|
[NCBI]
|
4.671e-05
|
|
|
NOL3
|
[NCBI]
|
4.671e-05
|
|
|
PRSS15
|
[NCBI]
|
4.671e-05
|
|
|
SLC25A32
|
[NCBI]
|
4.671e-05
|
|
|
SHMT2
|
[NCBI]
|
4.671e-05
|
|
|
BCAT2
|
[NCBI]
|
4.671e-05
|
|
|
NDUFA1
|
[NCBI]
|
4.671e-05
|
|
|
MTTH
|
[NCBI]
|
4.671e-05
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
4.60431e-05
|
|
|
TP53
|
[NCBI]
|
4.59811e-05
|
|
|
ALS1
|
[NCBI]
|
4.50693e-05
|
|
|
LPL
|
[NCBI]
|
4.48102e-05
|
|
|
chloramphenicol toxicity
|
[NCBI]
|
4.47505e-05
|
|
|
CYP11B2
|
[NCBI]
|
4.37537e-05
|
|
|
ALD
|
[NCBI]
|
4.32435e-05
|
|
|
DHFR
|
[NCBI]
|
4.26866e-05
|
|
|
PPIF
|
[NCBI]
|
4.25146e-05
|
|
|
PMPCB
|
[NCBI]
|
4.25146e-05
|
|
|
BAD
|
[NCBI]
|
4.25146e-05
|
|
|
COX10
|
[NCBI]
|
4.25146e-05
|
|
|
COQ7
|
[NCBI]
|
4.25146e-05
|
|
|
MCCC2
|
[NCBI]
|
4.25146e-05
|
|
|
canavan disease
|
[NCBI]
|
4.21579e-05
|
|
|
NPPA
|
[NCBI]
|
4.046e-05
|
|
|
FTD
|
[NCBI]
|
4.04201e-05
|
|
|
aging
|
[NCBI]
|
3.9824e-05
|
|
|
vitamin d-dependent rickets, type i
|
[NCBI]
|
3.9824e-05
|
|
|
MDH2
|
[NCBI]
|
3.93161e-05
|
|
|
MTTF
|
[NCBI]
|
3.93161e-05
|
|
|
CLIC4
|
[NCBI]
|
3.93161e-05
|
|
|
TXNRD2
|
[NCBI]
|
3.93161e-05
|
|
|
AADAT
|
[NCBI]
|
3.93161e-05
|
|
|
SDHB
|
[NCBI]
|
3.93161e-05
|
|
|
ME1
|
[NCBI]
|
3.93161e-05
|
|
|
NOS3
|
[NCBI]
|
3.8204e-05
|
|
|
CAT
|
[NCBI]
|
3.81663e-05
|
|
|
CASP3
|
[NCBI]
|
3.80552e-05
|
|
|
EGFR
|
[NCBI]
|
3.76161e-05
|
|
|
DUT
|
[NCBI]
|
3.67314e-05
|
|
|
RPS13
|
[NCBI]
|
3.67314e-05
|
|
|
SLC25A13
|
[NCBI]
|
3.67314e-05
|
|
|
KIF1B
|
[NCBI]
|
3.67314e-05
|
|
|
SLOS
|
[NCBI]
|
3.67113e-05
|
|
|
GAPDH
|
[NCBI]
|
3.60432e-05
|
|
|
GNRH1
|
[NCBI]
|
3.48659e-05
|
|
|
UXT
|
[NCBI]
|
3.45645e-05
|
|
|
PDCD5
|
[NCBI]
|
3.45645e-05
|
|
|
DNAJA3
|
[NCBI]
|
3.45645e-05
|
|
|
DISC1
|
[NCBI]
|
3.44835e-05
|
|
|
ALDH2
|
[NCBI]
|
3.36894e-05
|
|
|
ATPAF2
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A45
|
[NCBI]
|
3.32656e-05
|
|
|
NDUFB8
|
[NCBI]
|
3.32656e-05
|
|
|
IDH3B
|
[NCBI]
|
3.32656e-05
|
|
|
PDK1
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A38
|
[NCBI]
|
3.32656e-05
|
|
|
C2ORF34
|
[NCBI]
|
3.32656e-05
|
|
|
COX19
|
[NCBI]
|
3.32656e-05
|
|
|
PDK2
|
[NCBI]
|
3.32656e-05
|
|
|
DDX28
|
[NCBI]
|
3.32656e-05
|
|
|
ATP5D
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A21
|
[NCBI]
|
3.32656e-05
|
|
|
DCI
|
[NCBI]
|
3.32656e-05
|
|
|
NDUFA7
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A34
|
[NCBI]
|
3.32656e-05
|
|
|
GTPBP3
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A35
|
[NCBI]
|
3.32656e-05
|
|
|
CABC1
|
[NCBI]
|
3.32656e-05
|
|
|
MOAP1
|
[NCBI]
|
3.32656e-05
|
|
|
GFM2
|
[NCBI]
|
3.32656e-05
|
|
|
sra stem loop-interacting rna-binding protein
|
[NCBI]
|
3.32656e-05
|
|
|
ATP5G3
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A24
|
[NCBI]
|
3.32656e-05
|
|
|
MARS2
|
[NCBI]
|
3.32656e-05
|
|
|
RTN4IP1
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A30
|
[NCBI]
|
3.32656e-05
|
|
|
p53-regulated apoptosis-inducing protein 1
|
[NCBI]
|
3.32656e-05
|
|
|
COX18
|
[NCBI]
|
3.32656e-05
|
|
|
TOP1MT
|
[NCBI]
|
3.32656e-05
|
|
|
dendritic cell ubiquitin-like protein
|
[NCBI]
|
3.32656e-05
|
|
|
LDHD
|
[NCBI]
|
3.32656e-05
|
|
|
OPA3
|
[NCBI]
|
3.32656e-05
|
|
|
NDUFA3
|
[NCBI]
|
3.32656e-05
|
|
|
MTX2
|
[NCBI]
|
3.32656e-05
|
|
|
ATP5F1
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A42
|
[NCBI]
|
3.32656e-05
|
|
|
methionine aminopeptidase 1d
|
[NCBI]
|
3.32656e-05
|
|
|
mitochondrial protein, 18-kd
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A44
|
[NCBI]
|
3.32656e-05
|
|
|
PTRH2
|
[NCBI]
|
3.32656e-05
|
|
|
AFG3L2
|
[NCBI]
|
3.32656e-05
|
|
|
ras-like gtpase gene
|
[NCBI]
|
3.32656e-05
|
|
|
hepatocellular carcinoma-downregulated mitochondrial carrier protein
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A41
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A26
|
[NCBI]
|
3.32656e-05
|
|
|
SUPV3L1
|
[NCBI]
|
3.32656e-05
|
|
|
COX11
|
[NCBI]
|
3.32656e-05
|
|
|
ABCB10
|
[NCBI]
|
3.32656e-05
|
|
|
DNAJC19
|
[NCBI]
|
3.32656e-05
|
|
|
ABCB8
|
[NCBI]
|
3.32656e-05
|
|
|
NFS1
|
[NCBI]
|
3.32656e-05
|
|
|
GTPBP5
|
[NCBI]
|
3.32656e-05
|
|
|
GCAT
|
[NCBI]
|
3.32656e-05
|
|
|
ATPAF1
|
[NCBI]
|
3.32656e-05
|
|
|
FARS2
|
[NCBI]
|
3.32656e-05
|
|
|
YARS2
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A46
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A39
|
[NCBI]
|
3.32656e-05
|
|
|
GTPBP10
|
[NCBI]
|
3.32656e-05
|
|
|
GRPEL1
|
[NCBI]
|
3.32656e-05
|
|
|
MARCH5
|
[NCBI]
|
3.32656e-05
|
|
|
PDK3
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A28
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A43
|
[NCBI]
|
3.32656e-05
|
|
|
OXSM
|
[NCBI]
|
3.32656e-05
|
|
|
PET112L
|
[NCBI]
|
3.32656e-05
|
|
|
NDUFB4
|
[NCBI]
|
3.32656e-05
|
|
|
SSBP1
|
[NCBI]
|
3.32656e-05
|
|
|
VDAC4
|
[NCBI]
|
3.32656e-05
|
|
|
NDUFC2
|
[NCBI]
|
3.32656e-05
|
|
|
NDUFB2
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A23
|
[NCBI]
|
3.32656e-05
|
|
|
WARS2
|
[NCBI]
|
3.32656e-05
|
|
|
SLC25A40
|
[NCBI]
|
3.32656e-05
|
|
|
TNF
|
[NCBI]
|
3.31494e-05
|
|
|
BCL2
|
[NCBI]
|
3.30138e-05
|
|
|
MTTI
|
[NCBI]
|
3.27009e-05
|
|
|
HTN3
|
[NCBI]
|
3.27009e-05
|
|
|
RTT
|
[NCBI]
|
3.25362e-05
|
|
|
CDS
|
[NCBI]
|
3.23445e-05
|
|
|
alexander disease
|
[NCBI]
|
3.23445e-05
|
|
|
GLDC
|
[NCBI]
|
3.10678e-05
|
|
|
septooptic dysplasia
|
[NCBI]
|
3.08179e-05
|
|
|
TG
|
[NCBI]
|
3.05762e-05
|
|
|
CKM
|
[NCBI]
|
2.96159e-05
|
|
|
HADH
|
[NCBI]
|
2.96159e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
2.93958e-05
|
|
|
glutaric acidemia i
|
[NCBI]
|
2.93958e-05
|
|
|
BCL2L11
|
[NCBI]
|
2.83103e-05
|
|
|
CPT1A
|
[NCBI]
|
2.83103e-05
|
|
|
SNN
|
[NCBI]
|
2.83103e-05
|
|
|
CYP11A1
|
[NCBI]
|
2.83103e-05
|
|
|
diabetes insipidus, nephrogenic, x-linked
|
[NCBI]
|
2.80663e-05
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
2.80663e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
2.80663e-05
|
|
|
ALPS
|
[NCBI]
|
2.7572e-05
|
|
|
PPOX
|
[NCBI]
|
2.71251e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
2.68199e-05
|
|
|
PDHA1
|
[NCBI]
|
2.67189e-05
|
|
|
APAF1
|
[NCBI]
|
2.60411e-05
|
|
|
obesity
|
[NCBI]
|
2.56481e-05
|
|
|
PXMP3
|
[NCBI]
|
2.5043e-05
|
|
|
NR4A1
|
[NCBI]
|
2.5043e-05
|
|
|
pyruvate carboxylase deficiency
|
[NCBI]
|
2.45438e-05
|
|
|
NGFB
|
[NCBI]
|
2.44462e-05
|
|
|
PHB
|
[NCBI]
|
2.41191e-05
|
|
|
ACACA
|
[NCBI]
|
2.41191e-05
|
|
|
SYNJ2BP
|
[NCBI]
|
2.33532e-05
|
|
|
ECSIT
|
[NCBI]
|
2.33532e-05
|
|
|
SLC25A10
|
[NCBI]
|
2.33532e-05
|
|
|
ADM2
|
[NCBI]
|
2.33532e-05
|
|
|
AKAP1
|
[NCBI]
|
2.33532e-05
|
|
|
PPM2C
|
[NCBI]
|
2.33532e-05
|
|
|
IARS
|
[NCBI]
|
2.33532e-05
|
|
|
UQCRFS1
|
[NCBI]
|
2.33532e-05
|
|
|
TIMM50
|
[NCBI]
|
2.33532e-05
|
|
|
MRPL3
|
[NCBI]
|
2.33532e-05
|
|
|
TIMM17A
|
[NCBI]
|
2.33532e-05
|
|
|
PEX11G
|
[NCBI]
|
2.33532e-05
|
|
|
DMGDH
|
[NCBI]
|
2.33532e-05
|
|
|
MMSDH
|
[NCBI]
|
2.33532e-05
|
|
|
AKAP10
|
[NCBI]
|
2.33532e-05
|
|
|
TIMM44
|
[NCBI]
|
2.33532e-05
|
|
|
ACAD8
|
[NCBI]
|
2.33532e-05
|
|
|
LRPPRC
|
[NCBI]
|
2.33532e-05
|
|
|
IAN4L1
|
[NCBI]
|
2.33532e-05
|
|
|
NDUFA12L
|
[NCBI]
|
2.33532e-05
|
|
|
VDAC3
|
[NCBI]
|
2.33532e-05
|
|
|
transducer of regulated camp response element-binding protein 3
|
[NCBI]
|
2.33532e-05
|
|
|
MYCBP
|
[NCBI]
|
2.33532e-05
|
|
|
TDRD1
|
[NCBI]
|
2.33532e-05
|
|
|
PTPMT1
|
[NCBI]
|
2.33532e-05
|
|
|
CMPK2
|
[NCBI]
|
2.33532e-05
|
|
|
MULK
|
[NCBI]
|
2.33532e-05
|
|
|
ARL2
|
[NCBI]
|
2.33532e-05
|
|
|
JTB
|
[NCBI]
|
2.33532e-05
|
|
|
SLC9A6
|
[NCBI]
|
2.33532e-05
|
|
|
GLY B+
|
[NCBI]
|
2.33532e-05
|
|
|
NDUFAF1
|
[NCBI]
|
2.33532e-05
|
|
|
BCL2L12
|
[NCBI]
|
2.33532e-05
|
|
|
UQCRC2
|
[NCBI]
|
2.33532e-05
|
|
|
CHK
|
[NCBI]
|
2.33532e-05
|
|
|
ACAA2
|
[NCBI]
|
2.33532e-05
|
|
|
breast cancer cell 2
|
[NCBI]
|
2.33532e-05
|
|
|
MTTS2
|
[NCBI]
|
2.33532e-05
|
|
|
ECHS1
|
[NCBI]
|
2.33532e-05
|
|
|
TP53I3
|
[NCBI]
|
2.33532e-05
|
|
|
ABCB6
|
[NCBI]
|
2.33532e-05
|
|
|
PPM1B
|
[NCBI]
|
2.33532e-05
|
|
|
MTCH1
|
[NCBI]
|
2.33532e-05
|
|
|
FXC1
|
[NCBI]
|
2.33532e-05
|
|
|
MTTA
|
[NCBI]
|
2.33532e-05
|
|
|
LIAS
|
[NCBI]
|
2.33532e-05
|
|
|
RAF1
|
[NCBI]
|
2.32595e-05
|
|
|
TNFSF6
|
[NCBI]
|
2.31142e-05
|
|
|
refsum disease, infantile form
|
[NCBI]
|
2.25142e-05
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
2.25142e-05
|
|
|
MADD
|
[NCBI]
|
2.25142e-05
|
|
|
ACP5
|
[NCBI]
|
2.25086e-05
|
|
|
LGALS3
|
[NCBI]
|
2.24566e-05
|
|
|
PANK2
|
[NCBI]
|
2.17037e-05
|
|
|
DLD
|
[NCBI]
|
2.17037e-05
|
|
|
BIRC5
|
[NCBI]
|
2.17037e-05
|
|
|
PTHLH
|
[NCBI]
|
2.16783e-05
|
|
|
mucolipidosis iv
|
[NCBI]
|
2.15788e-05
|
|
|
TNFRSF10A
|
[NCBI]
|
2.09955e-05
|
|
|
TNFRSF10B
|
[NCBI]
|
2.00031e-05
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
1.98461e-05
|
|
|
hyperglycerolemia
|
[NCBI]
|
1.98461e-05
|
|
|
CNTF
|
[NCBI]
|
1.98104e-05
|
|
|
NDUFA2
|
[NCBI]
|
1.96563e-05
|
|
|
ATP5B
|
[NCBI]
|
1.96563e-05
|
|
|
NDUFC1
|
[NCBI]
|
1.96563e-05
|
|
|
RPS10
|
[NCBI]
|
1.96563e-05
|
|
|
PEX11A
|
[NCBI]
|
1.96563e-05
|
|
|
cd27-binding protein
|
[NCBI]
|
1.96563e-05
|
|
|
POLDIP2
|
[NCBI]
|
1.96563e-05
|
|
|
MTTN
|
[NCBI]
|
1.96563e-05
|
|
|
GZMM
|
[NCBI]
|
1.96563e-05
|
|
|
NDUFS5
|
[NCBI]
|
1.96563e-05
|
|
|
PACS2
|
[NCBI]
|
1.96563e-05
|
|
|
PEX11B
|
[NCBI]
|
1.96563e-05
|
|
|
ETHE1
|
[NCBI]
|
1.96563e-05
|
|
|
CYP2R1
|
[NCBI]
|
1.96563e-05
|
|
|
COX6B
|
[NCBI]
|
1.96563e-05
|
|
|
NDUFV2
|
[NCBI]
|
1.96563e-05
|
|
|
NDUFS6
|
[NCBI]
|
1.96563e-05
|
|
|
RPS11
|
[NCBI]
|
1.96563e-05
|
|
|
MAN2C1
|
[NCBI]
|
1.96563e-05
|
|
|
PTPRQ
|
[NCBI]
|
1.96563e-05
|
|
|
t-cell antigen receptor, gamma subunit, alternate reading frame protein
|
[NCBI]
|
1.96563e-05
|
|
|
DECR1
|
[NCBI]
|
1.96563e-05
|
|
|
GRIN2D
|
[NCBI]
|
1.96563e-05
|
|
|
ACP6
|
[NCBI]
|
1.96563e-05
|
|
|
HTATIP2
|
[NCBI]
|
1.96563e-05
|
|
|
NDUFB6
|
[NCBI]
|
1.96563e-05
|
|
|
LASS1
|
[NCBI]
|
1.96563e-05
|
|
|
SHMT1
|
[NCBI]
|
1.96563e-05
|
|
|
TIMM23
|
[NCBI]
|
1.96563e-05
|
|
|
POLG2
|
[NCBI]
|
1.96563e-05
|
|
|
GAPDHS
|
[NCBI]
|
1.96563e-05
|
|
|
FKBP8
|
[NCBI]
|
1.96563e-05
|
|
|
SLC25A16
|
[NCBI]
|
1.96563e-05
|
|
|
EI24
|
[NCBI]
|
1.96563e-05
|
|
|
COX15
|
[NCBI]
|
1.96563e-05
|
|
|
PREPL
|
[NCBI]
|
1.96563e-05
|
|
|
ASAH2
|
[NCBI]
|
1.96563e-05
|
|
|
CYC1
|
[NCBI]
|
1.96563e-05
|
|
|
HSPA1A
|
[NCBI]
|
1.90962e-05
|
|
|
TYMS
|
[NCBI]
|
1.87494e-05
|
|
|
CYP1A1
|
[NCBI]
|
1.8402e-05
|
|
|
FRAP1
|
[NCBI]
|
1.8184e-05
|
|
|
NEM3
|
[NCBI]
|
1.75436e-05
|
|
|
GLI3
|
[NCBI]
|
1.74678e-05
|
|
|
GZMB
|
[NCBI]
|
1.74678e-05
|
|
|
SPP1
|
[NCBI]
|
1.73044e-05
|
|
|
ALDH4A1
|
[NCBI]
|
1.72806e-05
|
|
|
UNG2
|
[NCBI]
|
1.72806e-05
|
|
|
PEX26
|
[NCBI]
|
1.72806e-05
|
|
|
MIPEP
|
[NCBI]
|
1.72806e-05
|
|
|
BCL2L10
|
[NCBI]
|
1.72806e-05
|
|
|
KLK6
|
[NCBI]
|
1.72806e-05
|
|
|
DNMBP
|
[NCBI]
|
1.72806e-05
|
|
|
PNPT1
|
[NCBI]
|
1.72806e-05
|
|
|
MTUS1
|
[NCBI]
|
1.72806e-05
|
|
|
BNIP3
|
[NCBI]
|
1.72806e-05
|
|
|
ATP5C1
|
[NCBI]
|
1.72806e-05
|
|
|
BZRP
|
[NCBI]
|
1.72806e-05
|
|
|
SARDH
|
[NCBI]
|
1.72806e-05
|
|
|
ARG2
|
[NCBI]
|
1.72806e-05
|
|
|
AARS
|
[NCBI]
|
1.72806e-05
|
|
|
ING3
|
[NCBI]
|
1.72806e-05
|
|
|
CORO1A
|
[NCBI]
|
1.72806e-05
|
|
|
KARS
|
[NCBI]
|
1.72806e-05
|
|
|
HCCS
|
[NCBI]
|
1.72806e-05
|
|
|
RPL27
|
[NCBI]
|
1.72806e-05
|
|
|
ALDH1B1
|
[NCBI]
|
1.72806e-05
|
|
|
PMAIP1
|
[NCBI]
|
1.72806e-05
|
|
|
NDFIP2
|
[NCBI]
|
1.72806e-05
|
|
|
GPAM
|
[NCBI]
|
1.72806e-05
|
|
|
MRPL13
|
[NCBI]
|
1.72806e-05
|
|
|
GZMH
|
[NCBI]
|
1.72806e-05
|
|
|
GRINA
|
[NCBI]
|
1.72806e-05
|
|
|
RPL11
|
[NCBI]
|
1.72806e-05
|
|
|
ACADSB
|
[NCBI]
|
1.72806e-05
|
|
|
AK3L1
|
[NCBI]
|
1.72806e-05
|
|
|
ACAD9
|
[NCBI]
|
1.72806e-05
|
|
|
PACS1
|
[NCBI]
|
1.72806e-05
|
|
|
PARP1
|
[NCBI]
|
1.72255e-05
|
|
|
pyruvate decarboxylase deficiency
|
[NCBI]
|
1.68445e-05
|
|
|
AHC
|
[NCBI]
|
1.68445e-05
|
|
|
FGF7
|
[NCBI]
|
1.63388e-05
|
|
|
RCDP1
|
[NCBI]
|
1.61758e-05
|
|
|
anemia, sideroblastic, x-linked
|
[NCBI]
|
1.56144e-05
|
|
|
SIRT1
|
[NCBI]
|
1.56144e-05
|
|
|
ENO2
|
[NCBI]
|
1.55322e-05
|
|
|
CS
|
[NCBI]
|
1.55322e-05
|
|
|
CASP7
|
[NCBI]
|
1.55322e-05
|
|
|
TRIP11
|
[NCBI]
|
1.55322e-05
|
|
|
COQ2
|
[NCBI]
|
1.55322e-05
|
|
|
TRAK1
|
[NCBI]
|
1.55322e-05
|
|
|
RBM3
|
[NCBI]
|
1.55322e-05
|
|
|
GPD1
|
[NCBI]
|
1.55322e-05
|
|
|
HK2
|
[NCBI]
|
1.55322e-05
|
|
|
MCCC1
|
[NCBI]
|
1.55322e-05
|
|
|
RIPK3
|
[NCBI]
|
1.55322e-05
|
|
|
KLF3
|
[NCBI]
|
1.55322e-05
|
|
|
SLC25A6
|
[NCBI]
|
1.55322e-05
|
|
|
SEPT4
|
[NCBI]
|
1.55322e-05
|
|
|
PTMA
|
[NCBI]
|
1.55322e-05
|
|
|
SH3GLB1
|
[NCBI]
|
1.55322e-05
|
|
|
GDNF
|
[NCBI]
|
1.50653e-05
|
|
|
SHBG
|
[NCBI]
|
1.44266e-05
|
|
|
PRKCB1
|
[NCBI]
|
1.41535e-05
|
|
|
MPV17
|
[NCBI]
|
1.41535e-05
|
|
|
HSPD1
|
[NCBI]
|
1.41535e-05
|
|
|
golgi-localized syntaphilin-related protein
|
[NCBI]
|
1.41535e-05
|
|
|
HIST1H1C
|
[NCBI]
|
1.41535e-05
|
|
|
HAX1
|
[NCBI]
|
1.41535e-05
|
|
|
PHB2
|
[NCBI]
|
1.41535e-05
|
|
|
NFATC4
|
[NCBI]
|
1.41535e-05
|
|
|
CARD12
|
[NCBI]
|
1.41535e-05
|
|
|
IFI6
|
[NCBI]
|
1.41535e-05
|
|
|
CKB
|
[NCBI]
|
1.41535e-05
|
|
|
CRAT
|
[NCBI]
|
1.41535e-05
|
|
|
TALDO1
|
[NCBI]
|
1.41535e-05
|
|
|
MTTS1
|
[NCBI]
|
1.41535e-05
|
|
|
AK2
|
[NCBI]
|
1.41535e-05
|
|
|
AHR
|
[NCBI]
|
1.40388e-05
|
|
|
TERT
|
[NCBI]
|
1.34213e-05
|
|
|
FPGS
|
[NCBI]
|
1.33696e-05
|
|
|
GRIA2
|
[NCBI]
|
1.33329e-05
|
|
|
CDSP
|
[NCBI]
|
1.32289e-05
|
|
|
pyruvate kinase deficiency of red cells
|
[NCBI]
|
1.32289e-05
|
|
|
TK2
|
[NCBI]
|
1.3019e-05
|
|
|
LITAF
|
[NCBI]
|
1.3019e-05
|
|
|
ELK1
|
[NCBI]
|
1.3019e-05
|
|
|
CYP24A1
|
[NCBI]
|
1.3019e-05
|
|
|
CASP2
|
[NCBI]
|
1.3019e-05
|
|
|
SPHK2
|
[NCBI]
|
1.3019e-05
|
|
|
HMGCS2
|
[NCBI]
|
1.3019e-05
|
|
|
humanin
|
[NCBI]
|
1.3019e-05
|
|
|
CASP9
|
[NCBI]
|
1.3019e-05
|
|
|
AMT
|
[NCBI]
|
1.3019e-05
|
|
|
GRIN2C
|
[NCBI]
|
1.3019e-05
|
|
|
SMCP
|
[NCBI]
|
1.3019e-05
|
|
|
C10ORF2
|
[NCBI]
|
1.3019e-05
|
|
|
CRTC2
|
[NCBI]
|
1.3019e-05
|
|
|
BTF3
|
[NCBI]
|
1.3019e-05
|
|
|
MAPK10
|
[NCBI]
|
1.3019e-05
|
|
|
GCSH
|
[NCBI]
|
1.3019e-05
|
|
|
down syndrome
|
[NCBI]
|
1.27086e-05
|
|
|
SCA7
|
[NCBI]
|
1.27086e-05
|
|
|
SRF
|
[NCBI]
|
1.25009e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
1.23621e-05
|
|
|
HPS
|
[NCBI]
|
1.23259e-05
|
|
|
VDR
|
[NCBI]
|
1.22611e-05
|
|
|
MDD
|
[NCBI]
|
1.22495e-05
|
|
|
ATM
|
[NCBI]
|
1.21863e-05
|
|
|
ENC1
|
[NCBI]
|
1.2058e-05
|
|
|
PTGES
|
[NCBI]
|
1.2058e-05
|
|
|
ACACB
|
[NCBI]
|
1.2058e-05
|
|
|
IREB2
|
[NCBI]
|
1.2058e-05
|
|
|
HADHB
|
[NCBI]
|
1.2058e-05
|
|
|
MCL1
|
[NCBI]
|
1.2058e-05
|
|
|
PPP2R4
|
[NCBI]
|
1.2058e-05
|
|
|
DGUOK
|
[NCBI]
|
1.2058e-05
|
|
|
GABPA
|
[NCBI]
|
1.2058e-05
|
|
|
ITPA
|
[NCBI]
|
1.2058e-05
|
|
|
SHC1
|
[NCBI]
|
1.2058e-05
|
|
|
BCAT1
|
[NCBI]
|
1.2058e-05
|
|
|
MECT1
|
[NCBI]
|
1.2058e-05
|
|
|
SYNJ2
|
[NCBI]
|
1.2058e-05
|
|
|
kartagener syndrome
|
[NCBI]
|
1.17274e-05
|
|
|
GYS1
|
[NCBI]
|
1.12267e-05
|
|
|
WASF1
|
[NCBI]
|
1.12267e-05
|
|
|
AK3
|
[NCBI]
|
1.12267e-05
|
|
|
HLA-DRB1
|
[NCBI]
|
1.12267e-05
|
|
|
OPHN1
|
[NCBI]
|
1.12267e-05
|
|
|
KIF5B
|
[NCBI]
|
1.12267e-05
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
1.12267e-05
|
|
|
FDX1
|
[NCBI]
|
1.12267e-05
|
|
|
TST
|
[NCBI]
|
1.12267e-05
|
|
|
GSS
|
[NCBI]
|
1.12267e-05
|
|
|
PDXK
|
[NCBI]
|
1.12267e-05
|
|
|
RIPK1
|
[NCBI]
|
1.12055e-05
|
|
|
GCK
|
[NCBI]
|
1.0678e-05
|
|
|
SLC2A3
|
[NCBI]
|
1.04963e-05
|
|
|
DGAT1
|
[NCBI]
|
1.04963e-05
|
|
|
ERN1
|
[NCBI]
|
1.04963e-05
|
|
|
YY1
|
[NCBI]
|
1.04963e-05
|
|
|
PRKCE
|
[NCBI]
|
1.04963e-05
|
|
|
GPX4
|
[NCBI]
|
1.04963e-05
|
|
|
SIRT2
|
[NCBI]
|
1.04963e-05
|
|
|
ITPR1
|
[NCBI]
|
1.04963e-05
|
|
|
GSR
|
[NCBI]
|
9.94187e-06
|
|
|
NFATC3
|
[NCBI]
|
9.84624e-06
|
|
|
CYP11B1
|
[NCBI]
|
9.84624e-06
|
|
|
NEFH
|
[NCBI]
|
9.84624e-06
|
|
|
MDH1
|
[NCBI]
|
9.84624e-06
|
|
|
PYCARD
|
[NCBI]
|
9.84624e-06
|
|
|
PARG
|
[NCBI]
|
9.70992e-06
|
|
|
STARD3
|
[NCBI]
|
9.262e-06
|
|
|
PTPN6
|
[NCBI]
|
9.262e-06
|
|
|
PIN1
|
[NCBI]
|
9.262e-06
|
|
|
SCCA1
|
[NCBI]
|
9.262e-06
|
|
|
UBB
|
[NCBI]
|
9.262e-06
|
|
|
CPS1
|
[NCBI]
|
9.262e-06
|
|
|
BIRC4
|
[NCBI]
|
9.262e-06
|
|
|
oncogene dj1
|
[NCBI]
|
9.262e-06
|
|
|
CERK
|
[NCBI]
|
9.262e-06
|
|
|
RASSF1
|
[NCBI]
|
9.262e-06
|
|
|
APS1
|
[NCBI]
|
9.1938e-06
|
|
|
AT
|
[NCBI]
|
8.98011e-06
|
|
|
TNFRSF10C
|
[NCBI]
|
8.73252e-06
|
|
|
SURF1
|
[NCBI]
|
8.73252e-06
|
|
|
TXN
|
[NCBI]
|
8.73252e-06
|
|
|
GDAP1
|
[NCBI]
|
8.73252e-06
|
|
|
PAK3
|
[NCBI]
|
8.73252e-06
|
|
|
RPS3
|
[NCBI]
|
8.73252e-06
|
|
|
TCL1A
|
[NCBI]
|
8.73252e-06
|
|
|
SLC3A1
|
[NCBI]
|
8.73252e-06
|
|
|
WAS
|
[NCBI]
|
8.73198e-06
|
|
|
CTSD
|
[NCBI]
|
8.24935e-06
|
|
|
LDHC
|
[NCBI]
|
8.24935e-06
|
|
|
DSCR1
|
[NCBI]
|
8.24935e-06
|
|
|
FOXA2
|
[NCBI]
|
8.24935e-06
|
|
|
NEFL
|
[NCBI]
|
8.24935e-06
|
|
|
CYGB
|
[NCBI]
|
8.24935e-06
|
|
|
SNCA
|
[NCBI]
|
8.24825e-06
|
|
|
PTK2
|
[NCBI]
|
8.08568e-06
|
|
|
GHRH
|
[NCBI]
|
7.85577e-06
|
|
|
GRIN2B
|
[NCBI]
|
7.80586e-06
|
|
|
PRKCA
|
[NCBI]
|
7.80586e-06
|
|
|
ANP32A
|
[NCBI]
|
7.80586e-06
|
|
|
POLD1
|
[NCBI]
|
7.80586e-06
|
|
|
HSF1
|
[NCBI]
|
7.80586e-06
|
|
|
DBT
|
[NCBI]
|
7.80586e-06
|
|
|
metachromatic leukodystrophy
|
[NCBI]
|
7.78863e-06
|
|
|
TLR4
|
[NCBI]
|
7.68558e-06
|
|
|
VCP
|
[NCBI]
|
7.52232e-06
|
|
|
HHT
|
[NCBI]
|
7.46751e-06
|
|
|
MEN2A
|
[NCBI]
|
7.46751e-06
|
|
|
G6PD
|
[NCBI]
|
7.46715e-06
|
|
|
MAPK9
|
[NCBI]
|
7.39675e-06
|
|
|
TAZ
|
[NCBI]
|
7.39675e-06
|
|
|
JUN
|
[NCBI]
|
7.39675e-06
|
|
|
GLUD1
|
[NCBI]
|
7.01771e-06
|
|
|
HSPCA
|
[NCBI]
|
7.01771e-06
|
|
|
PCCB
|
[NCBI]
|
7.01771e-06
|
|
|
CYP27B1
|
[NCBI]
|
7.01771e-06
|
|
|
GCDH
|
[NCBI]
|
6.66519e-06
|
|
|
CBL
|
[NCBI]
|
6.66519e-06
|
|
|
CTSB
|
[NCBI]
|
6.66519e-06
|
|
|
GRIN2A
|
[NCBI]
|
6.66519e-06
|
|
|
PMCH
|
[NCBI]
|
6.44462e-06
|
|
|
USF2
|
[NCBI]
|
6.33625e-06
|
|
|
KL
|
[NCBI]
|
6.33625e-06
|
|
|
PPARD
|
[NCBI]
|
6.33625e-06
|
|
|
TPO
|
[NCBI]
|
6.30225e-06
|
|
|
MAP4
|
[NCBI]
|
6.0284e-06
|
|
|
UNG
|
[NCBI]
|
6.0284e-06
|
|
|
HAP1
|
[NCBI]
|
6.0284e-06
|
|
|
MUT
|
[NCBI]
|
6.0284e-06
|
|
|
TF
|
[NCBI]
|
5.77764e-06
|
|
|
wilson disease
|
[NCBI]
|
5.76011e-06
|
|
|
NGB
|
[NCBI]
|
5.73953e-06
|
|
|
RPS19
|
[NCBI]
|
5.73953e-06
|
|
| <