|
OMIM |
Link |
Information gain |
01 |
|
VRNI
|
[NCBI]
|
0.0125264
|
|
|
SLE
|
[NCBI]
|
0.00377338
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.00271162
|
|
|
mannose 6-phosphate receptor recognition defect, lebanese type
|
[NCBI]
|
0.00264919
|
|
|
CLN9
|
[NCBI]
|
0.00176437
|
|
|
multiple mitochondrial dysfunctions syndrome
|
[NCBI]
|
0.00176437
|
|
|
ZS
|
[NCBI]
|
0.00173801
|
|
|
EGF
|
[NCBI]
|
0.00143432
|
|
|
CTGF
|
[NCBI]
|
0.00129867
|
|
|
TSD
|
[NCBI]
|
0.00118748
|
|
|
RA
|
[NCBI]
|
0.00117889
|
|
|
NPC1
|
[NCBI]
|
0.00112837
|
|
|
FA
|
[NCBI]
|
0.001076
|
|
|
methylmalonic aciduria and homocystinuria, cbld type
|
[NCBI]
|
0.00102269
|
|
|
cataract and cardiomyopathy
|
[NCBI]
|
0.00102269
|
|
|
methylmalonic aciduria and homocystinuria, cblf type
|
[NCBI]
|
0.00102269
|
|
|
maple syrup urine disease
|
[NCBI]
|
0.0010223
|
|
|
AIS
|
[NCBI]
|
0.000992183
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.000925244
|
|
|
progeroid syndrome, neonatal
|
[NCBI]
|
0.000925244
|
|
|
AT
|
[NCBI]
|
0.000903954
|
|
|
MSD
|
[NCBI]
|
0.000900859
|
|
|
MG
|
[NCBI]
|
0.000900841
|
|
|
HGPS
|
[NCBI]
|
0.000891835
|
|
|
tricarboxylic acid cycle, defect of
|
[NCBI]
|
0.000881313
|
|
|
E11S
|
[NCBI]
|
0.000881313
|
|
|
medium chain 3-ketoacyl-coa thiolase deficiency
|
[NCBI]
|
0.000881313
|
|
|
BN51T
|
[NCBI]
|
0.000881313
|
|
|
AD
|
[NCBI]
|
0.000849399
|
|
|
ALD
|
[NCBI]
|
0.000834543
|
|
|
mucolipidosis ii
|
[NCBI]
|
0.000833894
|
|
|
hypercholesterolemia, autosomal dominant
|
[NCBI]
|
0.00080069
|
|
|
mucopolysaccharidosis type vii
|
[NCBI]
|
0.000800122
|
|
|
ST3
|
[NCBI]
|
0.000795891
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
0.000761396
|
|
|
NPY
|
[NCBI]
|
0.000755469
|
|
|
neuraminidase deficiency
|
[NCBI]
|
0.000750306
|
|
|
CF
|
[NCBI]
|
0.000743409
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
0.000726677
|
|
|
ZLS
|
[NCBI]
|
0.00072574
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.00072574
|
|
|
refsum disease, infantile form
|
[NCBI]
|
0.000682439
|
|
|
mucolipidosis iv
|
[NCBI]
|
0.000662324
|
|
|
PBD
|
[NCBI]
|
0.000662324
|
|
|
WRN
|
[NCBI]
|
0.000638231
|
|
|
phosphoribosylpyrophosphate synthetase superactivity
|
[NCBI]
|
0.000633094
|
|
|
RCDP1
|
[NCBI]
|
0.000626836
|
|
|
metachromatic leukodystrophy
|
[NCBI]
|
0.000622485
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
0.00061219
|
|
|
PCD
|
[NCBI]
|
0.000599281
|
|
|
FGF7
|
[NCBI]
|
0.000596168
|
|
|
USH1E
|
[NCBI]
|
0.00057476
|
|
|
HHF7
|
[NCBI]
|
0.00057476
|
|
|
osteogenesis imperfecta, type v
|
[NCBI]
|
0.00057476
|
|
|
doughnut lesions of skull, familial
|
[NCBI]
|
0.00057476
|
|
|
breast cancer, 11-22 translocation associated
|
[NCBI]
|
0.00057476
|
|
|
cerebrohepatorenal syndrome, variant types
|
[NCBI]
|
0.00057476
|
|
|
acanthosis nigricans
|
[NCBI]
|
0.00057476
|
|
|
RDPA
|
[NCBI]
|
0.00057476
|
|
|
d-bifunctional protein deficiency
|
[NCBI]
|
0.000557283
|
|
|
HGF
|
[NCBI]
|
0.000536999
|
|
|
hurler syndrome
|
[NCBI]
|
0.000536061
|
|
|
mucopolysaccharidosis type iiib
|
[NCBI]
|
0.000534949
|
|
|
ACHE
|
[NCBI]
|
0.000533159
|
|
|
CRH
|
[NCBI]
|
0.00052808
|
|
|
infantile sialic acid storage disorder
|
[NCBI]
|
0.000526632
|
|
|
PRL
|
[NCBI]
|
0.000525367
|
|
|
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
|
[NCBI]
|
0.000524468
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000501252
|
|
|
holocarboxylase synthetase deficiency
|
[NCBI]
|
0.000488267
|
|
|
pyruvate decarboxylase deficiency
|
[NCBI]
|
0.000488245
|
|
|
succinyl-coa:3-oxoacid coa transferase deficiency
|
[NCBI]
|
0.000479496
|
|
|
LS
|
[NCBI]
|
0.00047784
|
|
|
gaucher disease, type i
|
[NCBI]
|
0.000475678
|
|
|
AVP
|
[NCBI]
|
0.000462123
|
|
|
saccharopinuria
|
[NCBI]
|
0.000461818
|
|
|
ehlers-danlos syndrome, type v
|
[NCBI]
|
0.000461818
|
|
|
gangliosidosis, gm2, type iii, or juvenile type
|
[NCBI]
|
0.000461818
|
|
|
USH2B
|
[NCBI]
|
0.000461818
|
|
|
ehlers-danlos syndrome, type iv, autosomal dominant
|
[NCBI]
|
0.000445405
|
|
|
acyl-coa dehydrogenase, short-chain, deficiency of
|
[NCBI]
|
0.000436443
|
|
|
CCK
|
[NCBI]
|
0.000434291
|
|
|
PTK2
|
[NCBI]
|
0.000430525
|
|
|
XPA
|
[NCBI]
|
0.000428388
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
0.000427698
|
|
|
MFS
|
[NCBI]
|
0.000422237
|
|
|
UCMD
|
[NCBI]
|
0.000415012
|
|
|
alpha-methylacetoacetic aciduria
|
[NCBI]
|
0.000415012
|
|
|
VIP
|
[NCBI]
|
0.000404161
|
|
|
CRC
|
[NCBI]
|
0.000401035
|
|
|
RP
|
[NCBI]
|
0.000392569
|
|
|
FECD2
|
[NCBI]
|
0.000390031
|
|
|
bruck syndrome 1
|
[NCBI]
|
0.000390031
|
|
|
spondyloepiphyseal dysplasia tarda, toledo type
|
[NCBI]
|
0.000390031
|
|
|
TKCR
|
[NCBI]
|
0.000390031
|
|
|
dermal ridges, patternless
|
[NCBI]
|
0.000390031
|
|
|
dupuytren contracture
|
[NCBI]
|
0.000390031
|
|
|
CJD
|
[NCBI]
|
0.000386603
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
0.000380905
|
|
|
donohue syndrome
|
[NCBI]
|
0.00037827
|
|
|
mucopolysaccharidosis type iiia
|
[NCBI]
|
0.00037827
|
|
|
acyl-coa dehydrogenase, very long-chain, deficiency of
|
[NCBI]
|
0.00037827
|
|
|
EBR1
|
[NCBI]
|
0.000369211
|
|
|
IVA
|
[NCBI]
|
0.000366134
|
|
|
CD
|
[NCBI]
|
0.000365436
|
|
|
RCDP3
|
[NCBI]
|
0.000361759
|
|
|
acyl-coa dehydrogenase, medium-chain, deficiency of
|
[NCBI]
|
0.000346246
|
|
|
pygmy
|
[NCBI]
|
0.00033779
|
|
|
ehlers-danlos syndrome, type viii
|
[NCBI]
|
0.00033779
|
|
|
MPO
|
[NCBI]
|
0.0003313
|
|
|
TH
|
[NCBI]
|
0.000323417
|
|
|
niemann-pick disease, type c2
|
[NCBI]
|
0.000321024
|
|
|
sialuria
|
[NCBI]
|
0.000316354
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
0.000309338
|
|
|
pyruvate carboxylase deficiency
|
[NCBI]
|
0.000309338
|
|
|
SLS
|
[NCBI]
|
0.000300303
|
|
|
fibrochondrogenesis
|
[NCBI]
|
0.000297062
|
|
|
metachromatic leukodystrophy due to saposin b deficiency
|
[NCBI]
|
0.00029675
|
|
|
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|
[NCBI]
|
0.00029675
|
|
|
mucolipidosis iiia
|
[NCBI]
|
0.000285685
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
0.000285685
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
0.000282997
|
|
|
insulin-like growth factor i, resistance to
|
[NCBI]
|
0.000280036
|
|
|
mucopolysaccharidosis type iiid
|
[NCBI]
|
0.000280036
|
|
|
pyruvate dehydrogenase phosphatase deficiency
|
[NCBI]
|
0.000280036
|
|
|
propionic acidemia
|
[NCBI]
|
0.000279527
|
|
|
argininosuccinic aciduria
|
[NCBI]
|
0.000279527
|
|
|
HEXA
|
[NCBI]
|
0.00027747
|
|
|
cutis laxa, x-linked
|
[NCBI]
|
0.000273534
|
|
|
gm1-gangliosidosis, type iii
|
[NCBI]
|
0.000273534
|
|
|
mucolipidosis iii, complementation group c
|
[NCBI]
|
0.000267157
|
|
|
glutathione synthetase deficiency
|
[NCBI]
|
0.000264183
|
|
|
AUTS4
|
[NCBI]
|
0.000263941
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
0.000262991
|
|
|
malonyl-coa decarboxylase deficiency
|
[NCBI]
|
0.000262182
|
|
|
menkes disease
|
[NCBI]
|
0.000260309
|
|
|
nijmegen breakage syndrome
|
[NCBI]
|
0.000259656
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
0.000251238
|
|
|
PPSH
|
[NCBI]
|
0.000250365
|
|
|
ehlers-danlos syndrome, type vii, autosomal recessive
|
[NCBI]
|
0.000250365
|
|
|
sandhoff disease
|
[NCBI]
|
0.000249013
|
|
|
krabbe disease
|
[NCBI]
|
0.000240607
|
|
|
CHAT
|
[NCBI]
|
0.000240022
|
|
|
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency
|
[NCBI]
|
0.000237811
|
|
|
wernicke-korsakoff syndrome
|
[NCBI]
|
0.000236227
|
|
|
COL1A1
|
[NCBI]
|
0.000235502
|
|
|
HPRT1
|
[NCBI]
|
0.000230741
|
|
|
BLM
|
[NCBI]
|
0.000228655
|
|
|
IFNB1
|
[NCBI]
|
0.000222747
|
|
|
methylmalonic aciduria, cbla type
|
[NCBI]
|
0.000218135
|
|
|
ehlers-danlos syndrome, type vii, autosomal dominant
|
[NCBI]
|
0.000218135
|
|
|
GFAP
|
[NCBI]
|
0.000216415
|
|
|
diabetes mellitus, insulin-resistant, with acanthosis nigricans
|
[NCBI]
|
0.000215383
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
0.000214628
|
|
|
EPO
|
[NCBI]
|
0.000213446
|
|
|
LNS
|
[NCBI]
|
0.000213436
|
|
|
corneal dystrophy, crystalline, of schnyder
|
[NCBI]
|
0.000212557
|
|
|
acroosteolysis with osteoporosis and changes in skull and mandible
|
[NCBI]
|
0.000212557
|
|
|
deafness, congenital, and onychodystrophy, recessive form
|
[NCBI]
|
0.000212557
|
|
|
PCCB
|
[NCBI]
|
0.000208017
|
|
|
PTH
|
[NCBI]
|
0.000205946
|
|
|
CEACAM5
|
[NCBI]
|
0.000205529
|
|
|
mucopolysaccharidosis type iiic
|
[NCBI]
|
0.000202221
|
|
|
CSA
|
[NCBI]
|
0.000202068
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
0.000201875
|
|
|
COL3A1
|
[NCBI]
|
0.000198925
|
|
|
ATLD
|
[NCBI]
|
0.000197791
|
|
|
citrullinemia, classic
|
[NCBI]
|
0.000196863
|
|
|
temporal arteritis
|
[NCBI]
|
0.000196365
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
0.000196157
|
|
|
MRD
|
[NCBI]
|
0.000192025
|
|
|
PWS
|
[NCBI]
|
0.000190535
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
0.000190429
|
|
|
PSAP
|
[NCBI]
|
0.000190092
|
|
|
FBN1
|
[NCBI]
|
0.000185349
|
|
|
COL1A2
|
[NCBI]
|
0.000184799
|
|
|
morquio syndrome b
|
[NCBI]
|
0.000181056
|
|
|
carnitine palmitoyltransferase i deficiency
|
[NCBI]
|
0.000181056
|
|
|
LRP1
|
[NCBI]
|
0.000178696
|
|
|
CDG2H
|
[NCBI]
|
0.000174776
|
|
|
pseudoacromegaly with severe insulin resistance
|
[NCBI]
|
0.000174776
|
|
|
CDG1C
|
[NCBI]
|
0.000174776
|
|
|
CDG1E
|
[NCBI]
|
0.000174776
|
|
|
3-@methylglutaconic aciduria, type iv
|
[NCBI]
|
0.000174776
|
|
|
epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase
|
[NCBI]
|
0.000174776
|
|
|
COXPD1
|
[NCBI]
|
0.000174776
|
|
|
hypercholesterolemia, autosomal dominant, type b
|
[NCBI]
|
0.000174776
|
|
|
KLK3
|
[NCBI]
|
0.000174395
|
|
|
MBP
|
[NCBI]
|
0.000174391
|
|
|
ACG1A
|
[NCBI]
|
0.000174
|
|
|
LMNA
|
[NCBI]
|
0.00017351
|
|
|
APC
|
[NCBI]
|
0.000171542
|
|
|
pyruvate dehydrogenase e3-binding protein deficiency
|
[NCBI]
|
0.000169493
|
|
|
adenylosuccinase deficiency
|
[NCBI]
|
0.000169493
|
|
|
RCDP2
|
[NCBI]
|
0.000169493
|
|
|
trifunctional protein deficiency
|
[NCBI]
|
0.00016687
|
|
|
molybdenum cofactor deficiency
|
[NCBI]
|
0.00016687
|
|
|
glycogen storage disease iv
|
[NCBI]
|
0.000165932
|
|
|
MADD
|
[NCBI]
|
0.000165932
|
|
|
PEX7
|
[NCBI]
|
0.000162417
|
|
|
GAN1
|
[NCBI]
|
0.000159296
|
|
|
VUR1
|
[NCBI]
|
0.000158025
|
|
|
RTS
|
[NCBI]
|
0.000157877
|
|
|
NPPA
|
[NCBI]
|
0.000155595
|
|
|
BL
|
[NCBI]
|
0.000154676
|
|
|
scheie syndrome
|
[NCBI]
|
0.000154591
|
|
|
homocystinuria
|
[NCBI]
|
0.000153765
|
|
|
refsum disease
|
[NCBI]
|
0.000152931
|
|
|
GUSB
|
[NCBI]
|
0.000150282
|
|
|
glycogen storage disease ii
|
[NCBI]
|
0.000149786
|
|
|
ALDH3A2
|
[NCBI]
|
0.000149444
|
|
|
XPG
|
[NCBI]
|
0.000148328
|
|
|
methylcobalamin deficiency, cblg type
|
[NCBI]
|
0.000148328
|
|
|
3-@methylglutaconic aciduria, type i
|
[NCBI]
|
0.000148328
|
|
|
BDNF
|
[NCBI]
|
0.000148188
|
|
|
IDUA
|
[NCBI]
|
0.000147797
|
|
|
LDLR
|
[NCBI]
|
0.000147688
|
|
|
niemann-pick disease, type b
|
[NCBI]
|
0.000145326
|
|
|
severe combined immunodeficiency with sensitivity to ionizing radiation
|
[NCBI]
|
0.000143794
|
|
|
aging
|
[NCBI]
|
0.000143794
|
|
|
mannosidosis, beta a, lysosomal
|
[NCBI]
|
0.000143794
|
|
|
hurler-scheie syndrome
|
[NCBI]
|
0.000143794
|
|
|
CDSP
|
[NCBI]
|
0.000143168
|
|
|
PCCA
|
[NCBI]
|
0.000134959
|
|
|
TNF
|
[NCBI]
|
0.000132837
|
|
|
hyperprolinemia, type ii
|
[NCBI]
|
0.000132046
|
|
|
schindler disease, type i
|
[NCBI]
|
0.000132046
|
|
|
de sanctis-cacchione syndrome
|
[NCBI]
|
0.000132046
|
|
|
cystinosis, adult nonnephropathic
|
[NCBI]
|
0.000132046
|
|
|
SRC
|
[NCBI]
|
0.000128932
|
|
|
AS
|
[NCBI]
|
0.000127126
|
|
|
PKS
|
[NCBI]
|
0.000126046
|
|
|
BTHS
|
[NCBI]
|
0.000126023
|
|
|
osteogenesis imperfecta, type iib
|
[NCBI]
|
0.000122
|
|
|
3-@methylcrotonyl-coa carboxylase 2 deficiency
|
[NCBI]
|
0.000122
|
|
|
combined saposin deficiency
|
[NCBI]
|
0.000122
|
|
|
lig4 syndrome
|
[NCBI]
|
0.000122
|
|
|
mevalonic aciduria
|
[NCBI]
|
0.000122
|
|
|
ACADVL
|
[NCBI]
|
0.000121135
|
|
|
ABCD1
|
[NCBI]
|
0.000120244
|
|
|
XPV
|
[NCBI]
|
0.000118861
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
0.000118861
|
|
|
FRDA
|
[NCBI]
|
0.000117477
|
|
|
ACADS
|
[NCBI]
|
0.000116816
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
0.000116816
|
|
|
PEX13
|
[NCBI]
|
0.000115492
|
|
|
FMF
|
[NCBI]
|
0.000114361
|
|
|
FSHMD1A
|
[NCBI]
|
0.00011365
|
|
|
SLC25A20
|
[NCBI]
|
0.000113643
|
|
|
CDS
|
[NCBI]
|
0.000110587
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
0.000109124
|
|
|
PEPD
|
[NCBI]
|
0.000108828
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
0.000108826
|
|
|
PEX12
|
[NCBI]
|
0.000108476
|
|
|
PEX1
|
[NCBI]
|
0.000108476
|
|
|
TP53
|
[NCBI]
|
0.000108107
|
|
|
PDHA1
|
[NCBI]
|
0.000108068
|
|
|
CFTR
|
[NCBI]
|
0.000107862
|
|
|
XPF
|
[NCBI]
|
0.000107831
|
|
|
ADCYAP1
|
[NCBI]
|
0.000106644
|
|
|
ATM
|
[NCBI]
|
0.000104514
|
|
|
TNFSF6
|
[NCBI]
|
0.000104087
|
|
|
HEXB
|
[NCBI]
|
0.000101854
|
|
|
AFP
|
[NCBI]
|
0.000101032
|
|
|
CDG1A
|
[NCBI]
|
9.96286e-05
|
|
|
phosphoglycerate dehydrogenase deficiency
|
[NCBI]
|
9.88747e-05
|
|
|
severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation
|
[NCBI]
|
9.88747e-05
|
|
|
3-@methylglutaconic aciduria, type iii
|
[NCBI]
|
9.88747e-05
|
|
|
CSB
|
[NCBI]
|
9.88747e-05
|
|
|
mismatch repair cancer syndrome
|
[NCBI]
|
9.88747e-05
|
|
|
ATP7A
|
[NCBI]
|
9.86988e-05
|
|
|
XPD
|
[NCBI]
|
9.83904e-05
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
9.80141e-05
|
|
|
gaucher disease, type iii
|
[NCBI]
|
9.80141e-05
|
|
|
XDH
|
[NCBI]
|
9.62018e-05
|
|
|
TG
|
[NCBI]
|
9.58341e-05
|
|
|
HSD17B4
|
[NCBI]
|
9.44968e-05
|
|
|
LIG4
|
[NCBI]
|
9.29174e-05
|
|
|
SLOS
|
[NCBI]
|
9.20235e-05
|
|
|
PLOD1
|
[NCBI]
|
9.14898e-05
|
|
|
SLC6A3
|
[NCBI]
|
9.06938e-05
|
|
|
galactose epimerase deficiency
|
[NCBI]
|
9.01732e-05
|
|
|
PDP
|
[NCBI]
|
9.01732e-05
|
|
|
RTT
|
[NCBI]
|
8.82305e-05
|
|
|
ribose 5-phosphate isomerase deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
surface polypeptides, anonymous
|
[NCBI]
|
8.73823e-05
|
|
|
contiguous abcd1/dxs1375e deletion syndrome
|
[NCBI]
|
8.73823e-05
|
|
|
dent disease 2
|
[NCBI]
|
8.73823e-05
|
|
|
growth factors, combined defect of
|
[NCBI]
|
8.73823e-05
|
|
|
CDG2D
|
[NCBI]
|
8.73823e-05
|
|
|
CDG1J
|
[NCBI]
|
8.73823e-05
|
|
|
mitochondrial phosphate carrier deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
hyperlysinemia due to defect in lysine transport into mitochondria
|
[NCBI]
|
8.73823e-05
|
|
|
methylmalonyl-coa epimerase deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
ACEE
|
[NCBI]
|
8.73823e-05
|
|
|
COXPD3
|
[NCBI]
|
8.73823e-05
|
|
|
infertile male syndrome
|
[NCBI]
|
8.73823e-05
|
|
|
XRS
|
[NCBI]
|
8.73823e-05
|
|
|
COXPD2
|
[NCBI]
|
8.73823e-05
|
|
|
aicar transformylase/imp cyclohydrolase, deficiency of
|
[NCBI]
|
8.73823e-05
|
|
|
optic atrophy 3, autosomal dominant
|
[NCBI]
|
8.73823e-05
|
|
|
deoxyribose-5-phosphate aldolase deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
zinc in breast milk, reduced
|
[NCBI]
|
8.73823e-05
|
|
|
spondylometaphyseal dysplasia with dentinogenesis imperfecta
|
[NCBI]
|
8.73823e-05
|
|
|
acid phosphatase deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
atpaf2 deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
mucopolysaccharidosis type viii
|
[NCBI]
|
8.73823e-05
|
|
|
pyruvate dehydrogenase e2 deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, infantile
|
[NCBI]
|
8.73823e-05
|
|
|
COXPD4
|
[NCBI]
|
8.73823e-05
|
|
|
CDG2B
|
[NCBI]
|
8.73823e-05
|
|
|
esterase es-2, regulator for
|
[NCBI]
|
8.73823e-05
|
|
|
isobutyryl-coa dehydrogenase deficiency
|
[NCBI]
|
8.73823e-05
|
|
|
methylmalonic aciduria, cblh type
|
[NCBI]
|
8.73823e-05
|
|
|
CDG1I
|
[NCBI]
|
8.73823e-05
|
|
|
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
|
[NCBI]
|
8.73823e-05
|
|
|
metachromasia of fibroblasts
|
[NCBI]
|
8.73823e-05
|
|
|
thyroid hormone metabolism, abnormal
|
[NCBI]
|
8.73823e-05
|
|
|
beta-hydroxyisobutyryl coa deacylase, deficiency of
|
[NCBI]
|
8.73823e-05
|
|
|
COFS4
|
[NCBI]
|
8.73823e-05
|
|
|
LDHCP
|
[NCBI]
|
8.73823e-05
|
|
|
CDG1H
|
[NCBI]
|
8.73823e-05
|
|
|
RESDX
|
[NCBI]
|
8.73823e-05
|
|
|
angiokeratoma corporis diffusum with arteriovenous fistulas
|
[NCBI]
|
8.73823e-05
|
|
|
fructose utilization
|
[NCBI]
|
8.73823e-05
|
|
|
spondyloepiphyseal dysplasia, omani type
|
[NCBI]
|
8.73823e-05
|
|
|
CDG1M
|
[NCBI]
|
8.73823e-05
|
|
|
OCRL
|
[NCBI]
|
8.72548e-05
|
|
|
MADA
|
[NCBI]
|
8.72548e-05
|
|
|
COL6A1
|
[NCBI]
|
8.72535e-05
|
|
|
fucosidosis
|
[NCBI]
|
8.72535e-05
|
|
|
OXCT1
|
[NCBI]
|
8.62779e-05
|
|
|
MMP3
|
[NCBI]
|
8.5259e-05
|
|
|
encephalopathy, ethylmalonic
|
[NCBI]
|
8.34151e-05
|
|
|
3-@methylcrotonyl-coa carboxylase 1 deficiency
|
[NCBI]
|
8.34151e-05
|
|
|
ehlers-danlos syndrome, progeroid form
|
[NCBI]
|
8.34151e-05
|
|
|
reifenstein syndrome
|
[NCBI]
|
8.34151e-05
|
|
|
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities
|
[NCBI]
|
8.29275e-05
|
|
|
GAA
|
[NCBI]
|
8.15067e-05
|
|
|
CDK2
|
[NCBI]
|
8.11638e-05
|
|
|
WAS
|
[NCBI]
|
7.91281e-05
|
|
|
ERCC5
|
[NCBI]
|
7.89703e-05
|
|
|
DRPLA
|
[NCBI]
|
7.83663e-05
|
|
|
leukoregulin
|
[NCBI]
|
7.8073e-05
|
|
|
COX15
|
[NCBI]
|
7.8073e-05
|
|
|
GBA
|
[NCBI]
|
7.77695e-05
|
|
|
PXE
|
[NCBI]
|
7.7294e-05
|
|
|
NPC2
|
[NCBI]
|
7.67257e-05
|
|
|
biotinidase deficiency
|
[NCBI]
|
7.64727e-05
|
|
|
gm1-gangliosidosis, type ii
|
[NCBI]
|
7.64727e-05
|
|
|
immunodeficiency-centromeric instability-facial anomalies syndrome
|
[NCBI]
|
7.64623e-05
|
|
|
CCL2
|
[NCBI]
|
7.56536e-05
|
|
|
OCP
|
[NCBI]
|
7.54888e-05
|
|
|
MJD
|
[NCBI]
|
7.42768e-05
|
|
|
sialuria, finnish type
|
[NCBI]
|
7.37002e-05
|
|
|
CPT1A
|
[NCBI]
|
7.28086e-05
|
|
|
phenylketonuria ii
|
[NCBI]
|
7.28086e-05
|
|
|
SRF
|
[NCBI]
|
7.21117e-05
|
|
|
elejalde disease
|
[NCBI]
|
7.18779e-05
|
|
|
hyperlipoproteinemia, type ii
|
[NCBI]
|
7.18779e-05
|
|
|
AOII
|
[NCBI]
|
7.18779e-05
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
7.17939e-05
|
|
|
XPC
|
[NCBI]
|
7.09251e-05
|
|
|
tight skin contracture syndrome, lethal
|
[NCBI]
|
7.06743e-05
|
|
|
KSR1
|
[NCBI]
|
7.02633e-05
|
|
|
SGSH
|
[NCBI]
|
7.02633e-05
|
|
|
SOD2
|
[NCBI]
|
6.97624e-05
|
|
|
NPC1
|
[NCBI]
|
6.86273e-05
|
|
|
CTSL
|
[NCBI]
|
6.78783e-05
|
|
|
wolman disease
|
[NCBI]
|
6.63211e-05
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
6.54297e-05
|
|
|
ZMPSTE24
|
[NCBI]
|
6.4952e-05
|
|
|
MLYCD
|
[NCBI]
|
6.4952e-05
|
|
|
GLB1
|
[NCBI]
|
6.44902e-05
|
|
|
CTNS
|
[NCBI]
|
6.42726e-05
|
|
|
NGFB
|
[NCBI]
|
6.31794e-05
|
|
|
peroxisomal acyl-coa oxidase deficiency
|
[NCBI]
|
6.27555e-05
|
|
|
formiminotransferase deficiency
|
[NCBI]
|
6.27555e-05
|
|
|
GS1
|
[NCBI]
|
6.27555e-05
|
|
|
pseudoxanthoma elasticum, forme fruste
|
[NCBI]
|
6.27555e-05
|
|
|
porphyria cutanea tarda, type i
|
[NCBI]
|
6.27555e-05
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
6.27555e-05
|
|
|
gaucher disease, perinatal lethal
|
[NCBI]
|
6.27555e-05
|
|
|
FBXO15
|
[NCBI]
|
6.20706e-05
|
|
|
NDUFS7
|
[NCBI]
|
6.20706e-05
|
|
|
POU5F1
|
[NCBI]
|
6.07253e-05
|
|
|
pulmonary fibrosis, idiopathic
|
[NCBI]
|
6.06587e-05
|
|
|
PEX6
|
[NCBI]
|
6.05577e-05
|
|
|
CDK4
|
[NCBI]
|
6.03114e-05
|
|
|
ACADM
|
[NCBI]
|
5.93281e-05
|
|
|
MVK
|
[NCBI]
|
5.83209e-05
|
|
|
fabry disease
|
[NCBI]
|
5.7886e-05
|
|
|
CDKN2A
|
[NCBI]
|
5.77449e-05
|
|
|
NANOG
|
[NCBI]
|
5.68118e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
5.56089e-05
|
|
|
MYC
|
[NCBI]
|
5.52856e-05
|
|
|
mitochondrial myopathy with diabetes
|
[NCBI]
|
5.52765e-05
|
|
|
glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to
|
[NCBI]
|
5.52765e-05
|
|
|
CDG2A
|
[NCBI]
|
5.52765e-05
|
|
|
hypoalphalipoproteinemia, primary
|
[NCBI]
|
5.52765e-05
|
|
|
hyperlysinemia
|
[NCBI]
|
5.52765e-05
|
|
|
FANCB
|
[NCBI]
|
5.52765e-05
|
|
|
PDHX
|
[NCBI]
|
5.42323e-05
|
|
|
PEX3
|
[NCBI]
|
5.42323e-05
|
|
|
ETFDH
|
[NCBI]
|
5.42323e-05
|
|
|
SLC22A5
|
[NCBI]
|
5.40202e-05
|
|
|
CPI
|
[NCBI]
|
5.40106e-05
|
|
|
PCNA
|
[NCBI]
|
5.39881e-05
|
|
|
NCOA6
|
[NCBI]
|
5.35503e-05
|
|
|
COL6A3
|
[NCBI]
|
5.35503e-05
|
|
|
CPT2
|
[NCBI]
|
5.35503e-05
|
|
|
CBP2
|
[NCBI]
|
5.35503e-05
|
|
|
VASP
|
[NCBI]
|
5.32417e-05
|
|
|
SRS
|
[NCBI]
|
5.27958e-05
|
|
|
ABCC1
|
[NCBI]
|
5.23138e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
5.20826e-05
|
|
|
MUT
|
[NCBI]
|
5.20826e-05
|
|
|
TNFAIP6
|
[NCBI]
|
5.20474e-05
|
|
|
SIAH2
|
[NCBI]
|
5.20474e-05
|
|
|
CHUK
|
[NCBI]
|
5.13832e-05
|
|
|
RNASE3
|
[NCBI]
|
5.11959e-05
|
|
|
GNPAT
|
[NCBI]
|
5.06656e-05
|
|
|
BCNS
|
[NCBI]
|
5.00573e-05
|
|
|
sarcosinemia
|
[NCBI]
|
4.94321e-05
|
|
|
3-@hydroxy-3-methylglutaryl-coa synthase 2, mitochondrial, deficiency of
|
[NCBI]
|
4.94321e-05
|
|
|
alpha-2-deficient collagen disease
|
[NCBI]
|
4.94321e-05
|
|
|
hyaluronan metabolism, defect in
|
[NCBI]
|
4.94321e-05
|
|
|
xeroderma pigmentosum ix
|
[NCBI]
|
4.94321e-05
|
|
|
long chain fatty acids, defect in transport of
|
[NCBI]
|
4.94321e-05
|
|
|
optic atrophy 1 and deafness
|
[NCBI]
|
4.94321e-05
|
|
|
carnitine acetyltransferase deficiency
|
[NCBI]
|
4.94321e-05
|
|
|
GUK2
|
[NCBI]
|
4.94321e-05
|
|
|
aromatic alpha-keto acid reductase
|
[NCBI]
|
4.94321e-05
|
|
|
morquio syndrome, nonkeratosulfate-excreting type
|
[NCBI]
|
4.94321e-05
|
|
|
hypospadias, x-linked
|
[NCBI]
|
4.94321e-05
|
|
|
hyaluronidase deficiency
|
[NCBI]
|
4.94321e-05
|
|
|
tyrosine aminotransferase, regulator of
|
[NCBI]
|
4.94321e-05
|
|
|
bruck syndrome 2
|
[NCBI]
|
4.94321e-05
|
|
|
CDG1F
|
[NCBI]
|
4.94321e-05
|
|
|
FANCD1
|
[NCBI]
|
4.94321e-05
|
|
|
colchicine resistance
|
[NCBI]
|
4.94321e-05
|
|
|
methylmalonic aciduria, cblb type
|
[NCBI]
|
4.94321e-05
|
|
|
irak4 deficiency
|
[NCBI]
|
4.94321e-05
|
|
|
glutaryl-coa oxidase deficiency
|
[NCBI]
|
4.94321e-05
|
|
|
intrauterine growth retardation with increased mitomycin c sensitivity
|
[NCBI]
|
4.94321e-05
|
|
|
creases, infra-auricular cutaneous, with tall stature and advanced bone age
|
[NCBI]
|
4.94321e-05
|
|
|
ARH
|
[NCBI]
|
4.8991e-05
|
|
|
HPS2
|
[NCBI]
|
4.8991e-05
|
|
|
E2F3
|
[NCBI]
|
4.87121e-05
|
|
|
AK2
|
[NCBI]
|
4.87121e-05
|
|
|
TNC
|
[NCBI]
|
4.83467e-05
|
|
|
DPYD
|
[NCBI]
|
4.80827e-05
|
|
|
PRPS1
|
[NCBI]
|
4.80827e-05
|
|
|
BSG
|
[NCBI]
|
4.7617e-05
|
|
|
OSM
|
[NCBI]
|
4.72071e-05
|
|
|
SMN2
|
[NCBI]
|
4.69416e-05
|
|
|
THRA
|
[NCBI]
|
4.69416e-05
|
|
|
ARSA
|
[NCBI]
|
4.63803e-05
|
|
|
AIC
|
[NCBI]
|
4.61739e-05
|
|
|
holoprosencephaly
|
[NCBI]
|
4.61739e-05
|
|
|
ERCC6
|
[NCBI]
|
4.5747e-05
|
|
|
MMP1
|
[NCBI]
|
4.54151e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
4.5198e-05
|
|
|
IL2
|
[NCBI]
|
4.47495e-05
|
|
|
PCK2
|
[NCBI]
|
4.44332e-05
|
|
|
BCKDHA
|
[NCBI]
|
4.44332e-05
|
|
|
DCLRE1C
|
[NCBI]
|
4.44332e-05
|
|
|
IRAK4
|
[NCBI]
|
4.44332e-05
|
|
|
INSR
|
[NCBI]
|
4.44264e-05
|
|
|
POMC
|
[NCBI]
|
4.41452e-05
|
|
|
galactokinase deficiency
|
[NCBI]
|
4.36122e-05
|
|
|
EBS2
|
[NCBI]
|
4.36122e-05
|
|
|
PCS
|
[NCBI]
|
4.36122e-05
|
|
|
FH
|
[NCBI]
|
4.25923e-05
|
|
|
TRAF2
|
[NCBI]
|
4.20641e-05
|
|
|
ALK
|
[NCBI]
|
4.17333e-05
|
|
|
XIST
|
[NCBI]
|
4.12529e-05
|
|
|
STAR
|
[NCBI]
|
4.11676e-05
|
|
|
HADHB
|
[NCBI]
|
4.09416e-05
|
|
|
ERCC4
|
[NCBI]
|
4.09416e-05
|
|
|
NAGLU
|
[NCBI]
|
4.09416e-05
|
|
|
E2F4
|
[NCBI]
|
4.09416e-05
|
|
|
MAP3K14
|
[NCBI]
|
4.09416e-05
|
|
|
MTTE
|
[NCBI]
|
4.09416e-05
|
|
|
HLCS
|
[NCBI]
|
4.09416e-05
|
|
|
GIP
|
[NCBI]
|
4.06429e-05
|
|
|
XPA
|
[NCBI]
|
4.00342e-05
|
|
|
KLF4
|
[NCBI]
|
3.98724e-05
|
|
|
MAG
|
[NCBI]
|
3.97549e-05
|
|
|
FGF1
|
[NCBI]
|
3.94708e-05
|
|
|
porphyria, congenital erythropoietic
|
[NCBI]
|
3.89464e-05
|
|
|
ATS
|
[NCBI]
|
3.89464e-05
|
|
|
canavan disease
|
[NCBI]
|
3.89464e-05
|
|
|
IGF1R
|
[NCBI]
|
3.88415e-05
|
|
|
DLST
|
[NCBI]
|
3.84922e-05
|
|
|
suppressor of variegation 3-9, drosophila, homolog of, 2
|
[NCBI]
|
3.84922e-05
|
|
|
GNPTG
|
[NCBI]
|
3.84922e-05
|
|
|
E2F5
|
[NCBI]
|
3.84922e-05
|
|
|
EFEMP2
|
[NCBI]
|
3.84922e-05
|
|
|
CARS
|
[NCBI]
|
3.84922e-05
|
|
|
PEX10
|
[NCBI]
|
3.84922e-05
|
|
|
ETFB
|
[NCBI]
|
3.84922e-05
|
|
|
UQCRB
|
[NCBI]
|
3.84922e-05
|
|
|
CAT
|
[NCBI]
|
3.83857e-05
|
|
|
TERT
|
[NCBI]
|
3.82975e-05
|
|
|
SOX2
|
[NCBI]
|
3.81875e-05
|
|
|
APTX
|
[NCBI]
|
3.81875e-05
|
|
|
ADAM10
|
[NCBI]
|
3.81875e-05
|
|
|
MTCO3
|
[NCBI]
|
3.81875e-05
|
|
|
OCRL
|
[NCBI]
|
3.79975e-05
|
|
|
SHBG
|
[NCBI]
|
3.70655e-05
|
|
|
PMCH
|
[NCBI]
|
3.69886e-05
|
|
|
DLD
|
[NCBI]
|
3.66291e-05
|
|
|
MAN2B1
|
[NCBI]
|
3.66291e-05
|
|
|
galactosemia
|
[NCBI]
|
3.6226e-05
|
|
|
PNMT
|
[NCBI]
|
3.59508e-05
|
|
|
melanoma-astrocytoma syndrome
|
[NCBI]
|
3.59342e-05
|
|
|
progeroid short stature with pigmented nevi
|
[NCBI]
|
3.59342e-05
|
|
|
CLN10
|
[NCBI]
|
3.59342e-05
|
|
|
ehlers-danlos-like syndrome due to tenascin-x deficiency
|
[NCBI]
|
3.59342e-05
|
|
|
cystinosis, late-onset juvenile or adolescent nephropathic type
|
[NCBI]
|
3.59342e-05
|
|
|
mucopolysaccharidoses, unclassified types
|
[NCBI]
|
3.59342e-05
|
|
|
CDG1G
|
[NCBI]
|
3.59342e-05
|
|
|
ARTS
|
[NCBI]
|
3.59342e-05
|
|
|
myopathy with storage of glycoproteins and glycosaminoglycans
|
[NCBI]
|
3.59342e-05
|
|
|
lathosterolosis
|
[NCBI]
|
3.59342e-05
|
|
|
immunodeficiency, partial combined, with absence of hla determinants and beta-2-microglobulin from lymphocytes
|
[NCBI]
|
3.59342e-05
|
|
|
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
|
[NCBI]
|
3.59342e-05
|
|
|
USH1F
|
[NCBI]
|
3.59342e-05
|
|
|
osteogenesis imperfecta, type vii
|
[NCBI]
|
3.59342e-05
|
|
|
fumarase deficiency
|
[NCBI]
|
3.59342e-05
|
|
|
PGK1
|
[NCBI]
|
3.5748e-05
|
|
|
TTR
|
[NCBI]
|
3.55998e-05
|
|
|
LOX
|
[NCBI]
|
3.55897e-05
|
|
|
TAGLN
|
[NCBI]
|
3.54575e-05
|
|
|
POLH
|
[NCBI]
|
3.54575e-05
|
|
|
CXCL1
|
[NCBI]
|
3.54575e-05
|
|
|
GDNF
|
[NCBI]
|
3.52785e-05
|
|
|
SMPD1
|
[NCBI]
|
3.51721e-05
|
|
|
pseudohypoparathyroidism, type ib
|
[NCBI]
|
3.48559e-05
|
|
|
omenn syndrome
|
[NCBI]
|
3.48559e-05
|
|
|
WBS
|
[NCBI]
|
3.47996e-05
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
3.45529e-05
|
|
|
CNTF
|
[NCBI]
|
3.44651e-05
|
|
|
bare lymphocyte syndrome, type ii
|
[NCBI]
|
3.42634e-05
|
|
|
TK1
|
[NCBI]
|
3.38051e-05
|
|
|
CMM
|
[NCBI]
|
3.36296e-05
|
|
|
IVD
|
[NCBI]
|
3.32284e-05
|
|
|
COL6A2
|
[NCBI]
|
3.32284e-05
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
3.2519e-05
|
|
|
H3F3A
|
[NCBI]
|
3.2519e-05
|
|
|
PCGF2
|
[NCBI]
|
3.24735e-05
|
|
|
GNPTAB
|
[NCBI]
|
3.24735e-05
|
|
|
AUH
|
[NCBI]
|
3.24735e-05
|
|
|
UBR1
|
[NCBI]
|
3.24735e-05
|
|
|
PLOD2
|
[NCBI]
|
3.24735e-05
|
|
|
DPM1
|
[NCBI]
|
3.24735e-05
|
|
|
MOCS2
|
[NCBI]
|
3.24735e-05
|
|
|
COG8
|
[NCBI]
|
3.24735e-05
|
|
|
PEX26
|
[NCBI]
|
3.24735e-05
|
|
|
PEX16
|
[NCBI]
|
3.24735e-05
|
|
|
MTRR
|
[NCBI]
|
3.24735e-05
|
|
|
ST5
|
[NCBI]
|
3.24735e-05
|
|
|
alpha-ketoglutarate dehydrogenase deficiency
|
[NCBI]
|
3.24735e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
3.14609e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
3.14609e-05
|
|
|
CGD
|
[NCBI]
|
3.14377e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
3.13781e-05
|
|
|
IFNAR1
|
[NCBI]
|
3.13058e-05
|
|
|
KCNQ1OT1
|
[NCBI]
|
3.12463e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
3.12397e-05
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
3.12397e-05
|
|
|
MCDC1
|
[NCBI]
|
3.12397e-05
|
|
|
AMH
|
[NCBI]
|
3.03003e-05
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
3.00748e-05
|
|
|
hla-d histocompatibility type
|
[NCBI]
|
3.00034e-05
|
|
|
NAGA
|
[NCBI]
|
2.94652e-05
|
|
|
BID
|
[NCBI]
|
2.94652e-05
|
|
|
SURF1
|
[NCBI]
|
2.94652e-05
|
|
|
DKC
|
[NCBI]
|
2.92407e-05
|
|
|
PPIF
|
[NCBI]
|
2.84035e-05
|
|
|
WASF2
|
[NCBI]
|
2.84035e-05
|
|
|
HGSNAT
|
[NCBI]
|
2.84035e-05
|
|
|
GFM1
|
[NCBI]
|
2.84035e-05
|
|
|
NHEJ1
|
[NCBI]
|
2.84035e-05
|
|
|
rad54, s. cerevisiae, homolog of, b
|
[NCBI]
|
2.84035e-05
|
|
|
MCCC2
|
[NCBI]
|
2.84035e-05
|
|
|
KLF15
|
[NCBI]
|
2.84035e-05
|
|
|
AGPS
|
[NCBI]
|
2.84035e-05
|
|
|
NBL1
|
[NCBI]
|
2.84035e-05
|
|
|
COX10
|
[NCBI]
|
2.84035e-05
|
|
|
TRADD
|
[NCBI]
|
2.84035e-05
|
|
|
NDUFS8
|
[NCBI]
|
2.84035e-05
|
|
|
CRTAP
|
[NCBI]
|
2.84035e-05
|
|
|
DHFR
|
[NCBI]
|
2.83255e-05
|
|
|
USH2A
|
[NCBI]
|
2.80211e-05
|
|
|
CTSD
|
[NCBI]
|
2.7851e-05
|
|
|
ACAT1
|
[NCBI]
|
2.7851e-05
|
|
|
DMD
|
[NCBI]
|
2.77802e-05
|
|
|
leigh syndrome, x-linked
|
[NCBI]
|
2.7634e-05
|
|
|
charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive
|
[NCBI]
|
2.7634e-05
|
|
|
gaucher disease, type iiic
|
[NCBI]
|
2.7634e-05
|
|
|
rapadilino syndrome
|
[NCBI]
|
2.7634e-05
|
|
|
AEXS
|
[NCBI]
|
2.7634e-05
|
|
|
hyalinosis, infantile systemic
|
[NCBI]
|
2.7634e-05
|
|
|
GRTH
|
[NCBI]
|
2.7634e-05
|
|
|
SPD2
|
[NCBI]
|
2.7634e-05
|
|
|
premature chromosome condensation with microcephaly and mental retardation
|
[NCBI]
|
2.7634e-05
|
|
|
acyl-coa dehydrogenase, long-chain, deficiency of
|
[NCBI]
|
2.7634e-05
|
|
|
UVS
|
[NCBI]
|
2.7634e-05
|
|
|
LSFC
|
[NCBI]
|
2.7634e-05
|
|
|
hyperglycerolemia
|
[NCBI]
|
2.71629e-05
|
|
|
EIF4E
|
[NCBI]
|
2.69958e-05
|
|
|
CCD
|
[NCBI]
|
2.68776e-05
|
|
|
SMAD3
|
[NCBI]
|
2.63775e-05
|
|
|
PXMP3
|
[NCBI]
|
2.63775e-05
|
|
|
ID1
|
[NCBI]
|
2.63775e-05
|
|
|
TKT
|
[NCBI]
|
2.63775e-05
|
|
|
RIPK1
|
[NCBI]
|
2.62911e-05
|
|
|
TERC
|
[NCBI]
|
2.61217e-05
|
|
|
PDSS2
|
[NCBI]
|
2.6023e-05
|
|
|
p53-regulated apoptosis-inducing protein 1
|
[NCBI]
|
2.6023e-05
|
|
|
ATIC
|
[NCBI]
|
2.6023e-05
|
|
|
RPIA
|
[NCBI]
|
2.6023e-05
|
|
|
TCF19
|
[NCBI]
|
2.6023e-05
|
|
|
AKAP8
|
[NCBI]
|
2.6023e-05
|
|
|
COX11
|
[NCBI]
|
2.6023e-05
|
|
|
A11
|
[NCBI]
|
2.6023e-05
|
|
|
CHMP5
|
[NCBI]
|
2.6023e-05
|
|
|
CTHRC1
|
[NCBI]
|
2.6023e-05
|
|
|
ARSC2
|
[NCBI]
|
2.6023e-05
|
|
|
CDC42EP2
|
[NCBI]
|
2.6023e-05
|
|
|
mmachc gene
|
[NCBI]
|
2.6023e-05
|
|
|
LIN9
|
[NCBI]
|
2.6023e-05
|
|
|
RASSF8
|
[NCBI]
|
2.6023e-05
|
|
|
PEPE
|
[NCBI]
|
2.6023e-05
|
|
|
RND2
|
[NCBI]
|
2.6023e-05
|
|
|
cell growth regulatory gene 11
|
[NCBI]
|
2.6023e-05
|
|
|
DISP2
|
[NCBI]
|
2.6023e-05
|
|
|
proapoptotic caspase adaptor protein
|
[NCBI]
|
2.6023e-05
|
|
|
complement component c1q, fibroblast type
|
[NCBI]
|
2.6023e-05
|
|
|
WRB
|
[NCBI]
|
2.6023e-05
|
|
|
HSPA9B
|
[NCBI]
|
2.6023e-05
|
|
|
ARID1A
|
[NCBI]
|
2.6023e-05
|
|
|
PEX5L
|
[NCBI]
|
2.6023e-05
|
|
|
CDC42EP5
|
[NCBI]
|
2.6023e-05
|
|
|
ST2
|
[NCBI]
|
2.6023e-05
|
|
|
raver1, mouse, homolog of
|
[NCBI]
|
2.6023e-05
|
|
|
DISP1
|
[NCBI]
|
2.6023e-05
|
|
|
CDH9
|
[NCBI]
|
2.6023e-05
|
|
|
PCDHGB4
|
[NCBI]
|
2.6023e-05
|
|
|
ZAKI4
|
[NCBI]
|
2.6023e-05
|
|
|
HAO2
|
[NCBI]
|
2.6023e-05
|
|
|
DCE
|
[NCBI]
|
2.6023e-05
|
|
|
nuclear-localized factor 2
|
[NCBI]
|
2.6023e-05
|
|
|
THAP1
|
[NCBI]
|
2.6023e-05
|
|
|
cell growth regulatory gene 19
|
[NCBI]
|
2.6023e-05
|
|
|
CDC42EP3
|
[NCBI]
|
2.6023e-05
|
|
|
HEXC
|
[NCBI]
|
2.6023e-05
|
|
|
ENO1B
|
[NCBI]
|
2.6023e-05
|
|
|
hsv-1 stimulation-related gene 1
|
[NCBI]
|
2.6023e-05
|
|
|
nck-associated protein 5
|
[NCBI]
|
2.6023e-05
|
|
|
ZFP62
|
[NCBI]
|
2.6023e-05
|
|
|
PET112L
|
[NCBI]
|
2.6023e-05
|
|
|
PCDH16
|
[NCBI]
|
2.6023e-05
|
|
|
COL22A1
|
[NCBI]
|
2.6023e-05
|
|
|
nuclear-localized factor 1
|
[NCBI]
|
2.6023e-05
|
|
|
FBS1
|
[NCBI]
|
2.6023e-05
|
|
|
nuclear-localized factor 3
|
[NCBI]
|
2.6023e-05
|
|
|
SAP30BP
|
[NCBI]
|
2.6023e-05
|
|
|
regulated in development and dna damage responses 2
|
[NCBI]
|
2.6023e-05
|
|
|
OPA3
|
[NCBI]
|
2.6023e-05
|
|
|
ADAMTS2
|
[NCBI]
|
2.6023e-05
|
|
|
HINT1
|
[NCBI]
|
2.6023e-05
|
|
|
ADAMTS10
|
[NCBI]
|
2.6023e-05
|
|
|
PSPHL
|
[NCBI]
|
2.6023e-05
|
|
|
HIBCH
|
[NCBI]
|
2.6023e-05
|
|
|
UQCR
|
[NCBI]
|
2.6023e-05
|
|
|
alg8, s. cerevisiae, homolog of
|
[NCBI]
|
2.6023e-05
|
|
|
XAB2
|
[NCBI]
|
2.6023e-05
|
|
|
alg2, s. cerevisiae, homolog of
|
[NCBI]
|
2.6023e-05
|
|
|
SPAG9
|
[NCBI]
|
2.53305e-05
|
|
|
MAP3K7IP2
|
[NCBI]
|
2.53305e-05
|
|
|
E2F2
|
[NCBI]
|
2.53305e-05
|
|
|
MDH2
|
[NCBI]
|
2.53305e-05
|
|
|
GGTA1
|
[NCBI]
|
2.53305e-05
|
|
|
TGFB1I1
|
[NCBI]
|
2.53305e-05
|
|
|
ENO3
|
[NCBI]
|
2.53305e-05
|
|
|
CSRP1
|
[NCBI]
|
2.53305e-05
|
|
|
RAD23B
|
[NCBI]
|
2.53305e-05
|
|
|
MAP3K2
|
[NCBI]
|
2.53305e-05
|
|
|
LOXL2
|
[NCBI]
|
2.53305e-05
|
|
|
MTR
|
[NCBI]
|
2.52292e-05
|
|
|
PTEN
|
[NCBI]
|
2.51446e-05
|
|
|
TTDP
|
[NCBI]
|
2.51409e-05
|
|
|
SMA3
|
[NCBI]
|
2.51409e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
2.51409e-05
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
2.51409e-05
|
|
|
VHL
|
[NCBI]
|
2.50987e-05
|
|
|
TNXB
|
[NCBI]
|
2.50244e-05
|
|
|
HADHA
|
[NCBI]
|
2.50244e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
2.49467e-05
|
|
|
PARP1
|
[NCBI]
|
2.4679e-05
|
|
|
IRF3
|
[NCBI]
|
2.43764e-05
|
|
|
PC
|
[NCBI]
|
2.43614e-05
|
|
|
APCS
|
[NCBI]
|
2.35606e-05
|
|
|
TNFRSF14
|
[NCBI]
|
2.35606e-05
|
|
|
SCA1
|
[NCBI]
|
2.3348e-05
|
|
|
ERCC8
|
[NCBI]
|
2.28713e-05
|
|
|
SLC25A5
|
[NCBI]
|
2.28713e-05
|
|
|
INPPL1
|
[NCBI]
|
2.28713e-05
|
|
|
CDH11
|
[NCBI]
|
2.28713e-05
|
|
|
PCAF
|
[NCBI]
|
2.28713e-05
|
|
|
LEPRE1
|
[NCBI]
|
2.28713e-05
|
|
|
HIST1H3C
|
[NCBI]
|
2.28713e-05
|
|
|
RPS13
|
[NCBI]
|
2.28713e-05
|
|
|
GBE1
|
[NCBI]
|
2.28713e-05
|
|
|
ICMT
|
[NCBI]
|
2.28713e-05
|
|
|
FGD4
|
[NCBI]
|
2.28713e-05
|
|
|
HMMR
|
[NCBI]
|
2.28713e-05
|
|
|
XRCC4
|
[NCBI]
|
2.28713e-05
|
|
|
CD6
|
[NCBI]
|
2.28713e-05
|
|
|
PSPH
|
[NCBI]
|
2.28713e-05
|
|
|
GAN
|
[NCBI]
|
2.28713e-05
|
|
|
RAC1
|
[NCBI]
|
2.27792e-05
|
|
|
DCN
|
[NCBI]
|
2.27792e-05
|
|
|
PGM3
|
[NCBI]
|
2.26174e-05
|
|
|
MYOD1
|
[NCBI]
|
2.26174e-05
|
|
|
NEU1
|
[NCBI]
|
2.26174e-05
|
|
|
EV
|
[NCBI]
|
2.24838e-05
|
|
|
MAPK3
|
[NCBI]
|
2.2201e-05
|
|
|
ABCA1
|
[NCBI]
|
2.203e-05
|
|
|
PPT1
|
[NCBI]
|
2.203e-05
|
|
|
IL6
|
[NCBI]
|
2.18117e-05
|
|
|
hyperpipecolatemia
|
[NCBI]
|
2.18023e-05
|
|
|
MLASA
|
[NCBI]
|
2.18023e-05
|
|
|
OUBR
|
[NCBI]
|
2.18023e-05
|
|
|
SMA4
|
[NCBI]
|
2.18023e-05
|
|
|
hypothyroidism, athyroidal, with spiky hair and cleft palate
|
[NCBI]
|
2.18023e-05
|
|
|
growth hormone insensitivity with immunodeficiency
|
[NCBI]
|
2.18023e-05
|
|
|
winchester syndrome
|
[NCBI]
|
2.18023e-05
|
|
|
glycogen storage disease 0, liver
|
[NCBI]
|
2.18023e-05
|
|
|
USH2C
|
[NCBI]
|
2.18023e-05
|
|
|
schneckenbecken dysplasia
|
[NCBI]
|
2.18023e-05
|
|
|
bile acid synthesis defect, congenital, 1
|
[NCBI]
|
2.18023e-05
|
|
|
LFS1
|
[NCBI]
|
2.18023e-05
|
|
|
ACG1B
|
[NCBI]
|
2.18023e-05
|
|
|
GRTH
|
[NCBI]
|
2.18023e-05
|
|
|
SMC
|
[NCBI]
|
2.18023e-05
|
|
|
d-2-@hydroxyglutaric aciduria
|
[NCBI]
|
2.18023e-05
|
|
|
XPB
|
[NCBI]
|
2.18023e-05
|
|
|
CES
|
[NCBI]
|
2.16273e-05
|
|
|
ALB
|
[NCBI]
|
2.15475e-05
|
|
|
ERCC1
|
[NCBI]
|
2.15396e-05
|
|
|
udp-n-acetylglucosamine 2-epimerase/n-acetylmannosamine kinase
|
[NCBI]
|
2.15396e-05
|
|
|
LPL
|
[NCBI]
|
2.11638e-05
|
|
|
PGR
|
[NCBI]
|
2.09948e-05
|
|
|
FBXW7
|
[NCBI]
|
2.08298e-05
|
|
|
NDUFS4
|
[NCBI]
|
2.08298e-05
|
|
|
PFKP
|
[NCBI]
|
2.08298e-05
|
|
|
ITPA
|
[NCBI]
|
2.08298e-05
|
|
|
ACP2
|
[NCBI]
|
2.08298e-05
|
|
|
GART
|
[NCBI]
|
2.08298e-05
|
|
|
RAD50
|
[NCBI]
|
2.08298e-05
|
|
|
PHYH
|
[NCBI]
|
2.08298e-05
|
|
|
CCNA2
|
[NCBI]
|
2.08298e-05
|
|
|
RECQL4
|
[NCBI]
|
2.08298e-05
|
|
|
AR
|
[NCBI]
|
2.0577e-05
|
|
|
ENPP1
|
[NCBI]
|
2.05329e-05
|
|
|
MRE11A
|
[NCBI]
|
2.05329e-05
|
|
|
LCP1
|
[NCBI]
|
2.05329e-05
|
|
|
ARNTL
|
[NCBI]
|
2.05329e-05
|
|
|
PDGFRB
|
[NCBI]
|
2.05329e-05
|
|
|
argininemia
|
[NCBI]
|
2.02168e-05
|
|
|
RB1
|
[NCBI]
|
2.01123e-05
|
|
|
NP
|
[NCBI]
|
1.97938e-05
|
|
|
GHRH
|
[NCBI]
|
1.95248e-05
|
|
|
PSEN1
|
[NCBI]
|
1.94904e-05
|
|
|
SPP1
|
[NCBI]
|
1.92102e-05
|
|
|
wilson disease
|
[NCBI]
|
1.91074e-05
|
|
|
PEPC
|
[NCBI]
|
1.90916e-05
|
|
|
IL2RB
|
[NCBI]
|
1.90916e-05
|
|
|
RNASEL
|
[NCBI]
|
1.90916e-05
|
|
|
TPM1
|
[NCBI]
|
1.90916e-05
|
|
|
PRKCD
|
[NCBI]
|
1.90916e-05
|
|
|
WASF1
|
[NCBI]
|
1.90916e-05
|
|
|
SUV39H1
|
[NCBI]
|
1.90916e-05
|
|
|
CYR61
|
[NCBI]
|
1.90916e-05
|
|
|
SIAH1
|
[NCBI]
|
1.90916e-05
|
|
|
AK3
|
[NCBI]
|
1.90916e-05
|
|
|
SDC2
|
[NCBI]
|
1.89947e-05
|
|
|
PLSCR1
|
[NCBI]
|
1.87041e-05
|
|
|
RPS6KA5
|
[NCBI]
|
1.87041e-05
|
|
|
PDGFB
|
[NCBI]
|
1.87041e-05
|
|
|
COMT
|
[NCBI]
|
1.83965e-05
|
|
|
TGFB1
|
[NCBI]
|
1.83437e-05
|
|
|
SST
|
[NCBI]
|
1.81058e-05
|
|
|
CCAL2
|
[NCBI]
|
1.81042e-05
|
|
|
GALC
|
[NCBI]
|
1.78701e-05
|
|
|
IFNGR1
|
[NCBI]
|
1.78701e-05
|
|
|
ERCC3
|
[NCBI]
|
1.7584e-05
|
|
|
MCOLN1
|
[NCBI]
|
1.7584e-05
|
|
|
MORF4
|
[NCBI]
|
1.7584e-05
|
|
|
SLC26A2
|
[NCBI]
|
1.7584e-05
|
|
|
POLB
|
[NCBI]
|
1.7584e-05
|
|
|
FBLN1
|
[NCBI]
|
1.7584e-05
|
|
|
PEX5
|
[NCBI]
|
1.7584e-05
|
|
|
XRCC5
|
[NCBI]
|
1.7584e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
1.7584e-05
|
|
|
BBC3
|
[NCBI]
|
1.7584e-05
|
|
|
CITED2
|
[NCBI]
|
1.7584e-05
|
|
|
IQGAP1
|
[NCBI]
|
1.7584e-05
|
|
|
ENPP2
|
[NCBI]
|
1.75353e-05
|
|
|
EGR1
|
[NCBI]
|
1.75353e-05
|
|
|
SMN1
|
[NCBI]
|
1.74385e-05
|
|
|
arbitrary restriction polymorphism 1
|
[NCBI]
|
1.74246e-05
|
|
|
gout, hprt-related
|
[NCBI]
|
1.74246e-05
|
|
|
GGM
|
[NCBI]
|
1.74246e-05
|
|
|
sturge-weber syndrome
|
[NCBI]
|
1.74246e-05
|
|
|
OPPG
|
[NCBI]
|
1.74246e-05
|
|
|
mitochondrial complex iii deficiency
|
[NCBI]
|
1.74246e-05
|
|
|
HIDS
|
[NCBI]
|
1.74246e-05
|
|
|
gaucher disease, atypical, due to saposin c deficiency
|
[NCBI]
|
1.74246e-05
|
|
|
USH1D
|
[NCBI]
|
1.74246e-05
|
|
|
lactic acidosis, fatal infantile
|
[NCBI]
|
1.74246e-05
|
|
|
creatine deficiency syndrome, x-linked
|
[NCBI]
|
1.74246e-05
|
|
|
PBT
|
[NCBI]
|
1.74246e-05
|
|
|
ERCC2
|
[NCBI]
|
1.70831e-05
|
|
|
ABCC6
|
[NCBI]
|
1.70831e-05
|
|
|
NPM1
|
[NCBI]
|
1.68574e-05
|
|
|
IHH
|
[NCBI]
|
1.66853e-05
|
|
|
VIM
|
[NCBI]
|
1.65498e-05
|
|
|
HP
|
[NCBI]
|
1.65286e-05
|
|
|
CYP1A1
|
[NCBI]
|
1.64226e-05
|
|
|
ARSB
|
[NCBI]
|
1.6339e-05
|
|
|
RECQL2
|
[NCBI]
|
1.6339e-05
|
|
|
TNP2
|
[NCBI]
|
1.62575e-05
|
|
|
SDHC
|
[NCBI]
|
1.62575e-05
|
|
|
NR1D1
|
[NCBI]
|
1.62575e-05
|
|
|
NQO1
|
[NCBI]
|
1.62575e-05
|
|
|
KEAP1
|
[NCBI]
|
1.62575e-05
|
|
|
SHANK2
|
[NCBI]
|
1.62362e-05
|
|
|
LIPB
|
[NCBI]
|
1.62362e-05
|
|
|
CGNL1
|
[NCBI]
|
1.62362e-05
|
|
|
SH3BP4
|
[NCBI]
|
1.62362e-05
|
|
|
DAZ2
|
[NCBI]
|
1.62362e-05
|
|
|
PLCD3
|
[NCBI]
|
1.62362e-05
|
|
|
IL17RC
|
[NCBI]
|
1.62362e-05
|
|
|
NCKAP1
|
[NCBI]
|
1.62362e-05
|
|
|
CDC37
|
[NCBI]
|
1.62362e-05
|
|
|
TWF1
|
[NCBI]
|
1.62362e-05
|
|
|
PDSS1
|
[NCBI]
|
1.62362e-05
|
|
|
PRMT6
|
[NCBI]
|
1.62362e-05
|
|
|
AASS
|
[NCBI]
|
1.62362e-05
|
|
|
MOCS1
|
[NCBI]
|
1.62362e-05
|
|
|
PLA2G3
|
[NCBI]
|
1.62362e-05
|
|
|
C10ORF39
|
[NCBI]
|
1.62362e-05
|
|
|
ATG4C
|
[NCBI]
|
1.62362e-05
|
|
|
CDC42EP4
|
[NCBI]
|
1.62362e-05
|
|
|
DGCR6L
|
[NCBI]
|
1.62362e-05
|
|
|
PDZD11
|
[NCBI]
|
1.62362e-05
|
|
|
HPS4
|
[NCBI]
|
1.62362e-05
|
|
|
PCDHGA12
|
[NCBI]
|
1.62362e-05
|
|
|
DAZ3
|
[NCBI]
|
1.62362e-05
|
|
|
regulated in development and dna damage responses 1
|
[NCBI]
|
1.62362e-05
|
|
|
MUTED
|
[NCBI]
|
1.62362e-05
|
|
|
DCLRE1B
|
[NCBI]
|
1.62362e-05
|
|
|
C5ORF13
|
[NCBI]
|
1.62362e-05
|
|
|
SUOX
|
[NCBI]
|
1.62362e-05
|
|
|
MMAA
|
[NCBI]
|
1.62362e-05
|
|
|
GBA3
|
[NCBI]
|
1.62362e-05
|
|
|
PEX11G
|
[NCBI]
|
1.62362e-05
|
|
|
RRN3
|
[NCBI]
|
1.62362e-05
|
|
|
FEA
|
[NCBI]
|
1.62362e-05
|
|
|
PLS3
|
[NCBI]
|
1.62362e-05
|
|
|
ALG6
|
[NCBI]
|
1.62362e-05
|
|
|
PCDH7
|
[NCBI]
|
1.62362e-05
|
|
|
YPEL1
|
[NCBI]
|
1.62362e-05
|
|
|
S5
|
[NCBI]
|
1.62362e-05
|
|
|
TACC2
|
[NCBI]
|
1.62362e-05
|
|
|
GYG2
|
[NCBI]
|
1.62362e-05
|
|
|
sarcomeric muscle protein
|
[NCBI]
|
1.62362e-05
|
|
|
CDC42EP1
|
[NCBI]
|
1.62362e-05
|
|
|
AP3M1
|
[NCBI]
|
1.62362e-05
|
|
|
ARSF
|
[NCBI]
|
1.62362e-05
|
|
|
JAKMIP1
|
[NCBI]
|
1.62362e-05
|
|
|
NAP1L4
|
[NCBI]
|
1.62362e-05
|
|
|
SRPX2
|
[NCBI]
|
1.62362e-05
|
|
|
FSD1
|
[NCBI]
|
1.62362e-05
|
|
|
leucyl-trna synthetase, mitochondrial
|
[NCBI]
|
1.62362e-05
|
|
|
POMT2
|
[NCBI]
|
1.62362e-05
|
|
|
GPR48
|
[NCBI]
|
1.62362e-05
|
|
|
SAMD4A
|
[NCBI]
|
1.62362e-05
|
|
|
C3ORF28
|
[NCBI]
|
1.62362e-05
|
|
|
PRPSAP2
|
[NCBI]
|
1.62362e-05
|
|
|
NFKBIL2
|
[NCBI]
|
1.62362e-05
|
|
|
TPK1
|
[NCBI]
|
1.62362e-05
|
|
|
DGCR6
|
[NCBI]
|
1.62362e-05
|
|
|
LEO1
|
[NCBI]
|
1.62362e-05
|
|
|
ADAMTS4
|
[NCBI]
|
1.62362e-05
|
|
|
PECI
|
[NCBI]
|
1.62362e-05
|
|
|
NDUFA12L
|
[NCBI]
|
1.62362e-05
|
|
|
EPHA8
|
[NCBI]
|
1.62362e-05
|
|
|
RAPH1
|
[NCBI]
|
1.62362e-05
|
|
|
PLXNB3
|
[NCBI]
|
1.62362e-05
|
|
|
ACOT2
|
[NCBI]
|
1.62362e-05
|
|
|
CEMP1
|
[NCBI]
|
1.62362e-05
|
|
|
MESTIT1
|
[NCBI]
|
1.62362e-05
|
|
|
GYLTL1B
|
[NCBI]
|
1.62362e-05
|
|
|
COX7A2
|
[NCBI]
|
1.62362e-05
|
|
|
GMIP
|
[NCBI]
|
1.62362e-05
|
|
|
USP28
|
[NCBI]
|
1.62362e-05
|
|
|
PMP22
|
[NCBI]
|
1.62158e-05
|
|
|
PPARG
|
[NCBI]
|
1.61739e-05
|
|
|
PSACH
|
[NCBI]
|
1.58738e-05
|
|
|
SVAS
|
[NCBI]
|
1.56826e-05
|
|
|
MTATP6
|
[NCBI]
|
1.56343e-05
|
|
|
GK
|
[NCBI]
|
1.56343e-05
|
|
|
MAPK7
|
[NCBI]
|
1.56343e-05
|
|
|
GRP
|
[NCBI]
|
1.52831e-05
|
|
|
TD1
|
[NCBI]
|
1.50902e-05
|
|
|
CHH
|
[NCBI]
|
1.50902e-05
|
|
|
MPI
|
[NCBI]
|
1.50773e-05
|
|
|
PIN1
|
[NCBI]
|
1.50773e-05
|
|
|
TBK1
|
[NCBI]
|
1.50773e-05
|
|
|
BMI1
|
[NCBI]
|
1.50773e-05
|
|
|
PTS
|
[NCBI]
|
1.50773e-05
|
|
|
GADD45A
|
[NCBI]
|
1.50773e-05
|
|
|
SIX5
|
[NCBI]
|
1.50773e-05
|
|
|
ADSL
|
[NCBI]
|
1.50773e-05
|
|
|
LDLRAP1
|
[NCBI]
|
1.50773e-05
|
|
|
XBP1
|
[NCBI]
|
1.50773e-05
|
|
|
SMARCA4
|
[NCBI]
|
1.50773e-05
|
|
|
FANCD2
|
[NCBI]
|
1.50773e-05
|
|
|
CFB
|
[NCBI]
|
1.49656e-05
|
|
|
NBS1
|
[NCBI]
|
1.49656e-05
|
|
|
CAV1
|
[NCBI]
|
1.49656e-05
|
|
|
ACOX1
|
[NCBI]
|
1.49656e-05
|
|
|
atypical mycobacteriosis, familial
|
[NCBI]
|
1.4449e-05
|
|
|
COL7A1
|
[NCBI]
|
1.43304e-05
|
|
|
LCAT
|
[NCBI]
|
1.412e-05
|
|
|
GRB2
|
[NCBI]
|
1.4038e-05
|
|
|
ELN
|
[NCBI]
|
1.4038e-05
|
|
|
AP3B1
|
[NCBI]
|
1.40176e-05
|
|
|
ME2
|
[NCBI]
|
1.40176e-05
|
|
|
AL-A1
|
[NCBI]
|
1.40176e-05
|
|
|
PGD
|
[NCBI]
|
1.40176e-05
|
|
|
sulfocysteinuria
|
[NCBI]
|
1.40076e-05
|
|
|
epidermolysis bullosa dystrophica, pasini type
|
[NCBI]
|
1.40076e-05
|
|
|
noonan-like/multiple giant cell lesion syndrome
|
[NCBI]
|
1.40076e-05
|
|
|
CTLN2
|
[NCBI]
|
1.40076e-05
|
|
|
HRD
|
[NCBI]
|
1.40076e-05
|
|
|
TFPI2
|
[NCBI]
|
1.3726e-05
|
|
|
PML
|
[NCBI]
|
1.3726e-05
|
|
|
CLS
|
[NCBI]
|
1.35557e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
1.34552e-05
|
|
|
leber optic atrophy
|
[NCBI]
|
1.32355e-05
|
|
|
SIRT1
|
[NCBI]
|
1.31504e-05
|
|
|
AREG
|
[NCBI]
|
1.31504e-05
|
|
|
orotic aciduria i
|
[NCBI]
|
1.3059e-05
|
|
|
SPR
|
[NCBI]
|
1.3059e-05
|
|
|
APAF1
|
[NCBI]
|
1.3059e-05
|
|
|
GOT1
|
[NCBI]
|
1.3059e-05
|
|
|
PEPA
|
[NCBI]
|
1.3059e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
1.28669e-05
|
|
|
FGFR3
|
[NCBI]
|
1.26913e-05
|
|
|
PEX11A
|
[NCBI]
|
1.26647e-05
|
|
|
JUB
|
[NCBI]
|
1.26647e-05
|
|
|
SCO1
|
[NCBI]
|
1.26647e-05
|
|
|
IL3RA
|
[NCBI]
|
1.26647e-05
|
|
|
DYRK3
|
[NCBI]
|
1.26647e-05
|
|
|
jun dimerization protein 2
|
[NCBI]
|
1.26647e-05
|
|
|
NDUFA8
|
[NCBI]
|
1.26647e-05
|
|
|
EGLN3
|
[NCBI]
|
1.26647e-05
|
|
|
TMOD3
|
[NCBI]
|
1.26647e-05
|
|
|
lymphocyte cytosol polypeptide, 20-kd
|
[NCBI]
|
1.26647e-05
|
|
|
SOCS7
|
[NCBI]
|
1.26647e-05
|
|
|
ZBP1
|
[NCBI]
|
1.26647e-05
|
|
|
KIN
|
[NCBI]
|
1.26647e-05
|
|
|
NDUFB6
|
[NCBI]
|
1.26647e-05
|
|
|
PDLIM4
|
[NCBI]
|
1.26647e-05
|
|
|
PRKRA
|
[NCBI]
|
1.26647e-05
|
|
|
CUGBP1
|
[NCBI]
|
1.26647e-05
|
|
|
MNS1
|
[NCBI]
|
1.26647e-05
|
|
|
NFKBIL1
|
[NCBI]
|
1.26647e-05
|
|
|
LATS2
|
[NCBI]
|
1.26647e-05
|
|
|
TMEM15
|
[NCBI]
|
1.26647e-05
|
|
|
WISP1
|
[NCBI]
|
1.26647e-05
|
|
|
CNOT7
|
[NCBI]
|
1.26647e-05
|
|
|
RND1
|
[NCBI]
|
1.26647e-05
|
|
|
CCNE2
|
[NCBI]
|
1.26647e-05
|
|
|
SMURF2
|
[NCBI]
|
1.26647e-05
|
|
|
sds3, yeast, homolog of
|
[NCBI]
|
1.26647e-05
|
|
|
PLDN
|
[NCBI]
|
1.26647e-05
|
|
|
KCNK9
|
[NCBI]
|
1.26647e-05
|
|
|
GATM
|
[NCBI]
|
1.26647e-05
|
|
|
fructosamine 3-kinase
|
[NCBI]
|
1.26647e-05
|
|
|
MAGOH
|
[NCBI]
|
1.26647e-05
|
|
|
CHFR
|
[NCBI]
|
1.26647e-05
|
|
|
TPD52L1
|
[NCBI]
|
1.26647e-05
|
|
|
RHEB2
|
[NCBI]
|
1.26647e-05
|
|
|
vesicle amine transport protein 1
|
[NCBI]
|
1.26647e-05
|
|
|
KATNB1
|
[NCBI]
|
1.26647e-05
|
|
|
JAKMIP2
|
[NCBI]
|
1.26647e-05
|
|
|
HERC1
|
[NCBI]
|
1.26647e-05
|
|
|
MANBA
|
[NCBI]
|
1.26647e-05
|
|
|
QSCN6
|
[NCBI]
|
1.26647e-05
|
|
|
ALG12
|
[NCBI]
|
1.26647e-05
|
|
|
RPS20
|
[NCBI]
|
1.26647e-05
|
|
|
fuse-binding protein-interacting repressor
|
[NCBI]
|
1.26647e-05
|
|
|
CARD10
|
[NCBI]
|
1.26647e-05
|
|
|
ARPC5
|
[NCBI]
|
1.26647e-05
|
|
|
HYAL3
|
[NCBI]
|
1.26647e-05
|
|
|
DDT
|
[NCBI]
|
1.26647e-05
|
|
|
TUFM
|
[NCBI]
|
1.26647e-05
|
|
|
LARS
|
[NCBI]
|
1.26647e-05
|
|
|
SHROOM4
|
[NCBI]
|
1.26647e-05
|
|
|
LIMD1
|
[NCBI]
|
1.26647e-05
|
|
|
HERC3
|
[NCBI]
|
1.26647e-05
|
|
|
HARS
|
[NCBI]
|
1.26647e-05
|
|
|
ZBTB7
|
[NCBI]
|
1.26647e-05
|
|
|
SIRT4
|
[NCBI]
|
1.26647e-05
|
|
|
RRM2B
|
[NCBI]
|
1.26647e-05
|
|
|
LTBP4
|
[NCBI]
|
1.26647e-05
|
|
|
TRAM2
|
[NCBI]
|
1.26647e-05
|
|
|
DCLRE1A
|
[NCBI]
|
1.26647e-05
|
|
|
ADHFE1
|
[NCBI]
|
1.26647e-05
|
|
|
ISLR
|
[NCBI]
|
1.26647e-05
|
|
|
fructosamine 3-kinase-related protein
|
[NCBI]
|
1.26647e-05
|
|
|
C6ORF55
|
[NCBI]
|
1.26647e-05
|
|
|
PCNT2
|
[NCBI]
|
1.26647e-05
|
|
|
SDPR
|
[NCBI]
|
1.26647e-05
|
|
|
TIA1
|
[NCBI]
|
1.26647e-05
|
|
|
ANGPTL6
|
[NCBI]
|
1.26647e-05
|
|
|
ANKS1A
|
[NCBI]
|
1.26647e-05
|
|
|
MTHFD1L
|
[NCBI]
|
1.26647e-05
|
|
|
EGLN2
|
[NCBI]
|
1.26647e-05
|
|
|
NDUFS2
|
[NCBI]
|
1.26647e-05
|
|
|
retinoblastoma-associated factor 600
|
[NCBI]
|
1.26647e-05
|
|
|
IPW
|
[NCBI]
|
1.26647e-05
|
|
|
NSMAF
|
[NCBI]
|
1.26647e-05
|
|
|
DUSP7
|
[NCBI]
|
1.26647e-05
|
|
|
mitochondrial ribosomal protein s16: mrps16
|
[NCBI]
|
1.26647e-05
|
|
|
ALOX15
|
[NCBI]
|
1.26647e-05
|
|
|
MTTY
|
[NCBI]
|
1.26647e-05
|
|
|
MGAT2
|
[NCBI]
|
1.26647e-05
|
|
|
BRE
|
[NCBI]
|
1.26647e-05
|
|
|
LRDD
|
[NCBI]
|
1.26647e-05
|
|
|
MAN2C1
|
[NCBI]
|
1.26647e-05
|
|
|
MTSS1
|
[NCBI]
|
1.26647e-05
|
|
|
RND3
|
[NCBI]
|
1.26647e-05
|
|
|
ESA4
|
[NCBI]
|
1.26647e-05
|
|
|
CNO
|
[NCBI]
|
1.26647e-05
|
|
|
XPNPEP2
|
[NCBI]
|
1.26647e-05
|
|
|
SC5DL
|
[NCBI]
|
1.26647e-05
|
|
|
VGLL1
|
[NCBI]
|
1.26647e-05
|
|
|
TSFM
|
[NCBI]
|
1.26647e-05
|
|
|
MAP7
|
[NCBI]
|
1.26647e-05
|
|
|
CENTG2
|
[NCBI]
|
1.26647e-05
|
|
|
DRG2
|
[NCBI]
|
1.26647e-05
|
|
|
IFIT1
|
[NCBI]
|
1.26647e-05
|
|
|
G6PD
|
[NCBI]
|
1.26242e-05
|
|
|
MDM2
|
[NCBI]
|
1.26014e-05
|
|
|
GAMT
|
[NCBI]
|
1.26014e-05
|
|
|
CDKN1A
|
[NCBI]
|
1.26014e-05
|
|
|
GRPR
|
[NCBI]
|
1.26014e-05
|
|
|
THBS1
|
[NCBI]
|
1.21864e-05
|
|
|
PNPLA2
|
[NCBI]
|
1.21864e-05
|
|
|
DBT
|
[NCBI]
|
1.21864e-05
|
|
|
SLC6A8
|
[NCBI]
|
1.21864e-05
|
|
|
KLF5
|
[NCBI]
|
1.21864e-05
|
|
|
ACTB
|
[NCBI]
|
1.21864e-05
|
|
|
FANCC
|
[NCBI]
|
1.20773e-05
|
|
|
PSEN2
|
[NCBI]
|
1.20773e-05
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
1.20323e-05
|
|
|
CP
|
[NCBI]
|
1.18839e-05
|
|
|
MAOA
|
[NCBI]
|
1.16107e-05
|
|
|
CCL18
|
[NCBI]
|
1.13879e-05
|
|
|
GALK1
|
[NCBI]
|
1.13879e-05
|
|
|
DDR1
|
[NCBI]
|
1.13879e-05
|
|
|
JUN
|
[NCBI]
|
1.13879e-05
|
|
|
HMOX1
|
[NCBI]
|
1.13879e-05
|
|
|
XRCC9
|
[NCBI]
|
1.13879e-05
|
|
|
PPARBP
|
[NCBI]
|
1.13879e-05
|
|
|
RCC1
|
[NCBI]
|
1.13879e-05
|
|
|
GCH1
|
[NCBI]
|
1.13879e-05
|
|
|
EP300
|
[NCBI]
|
1.13879e-05
|
|
|
NMB
|
[NCBI]
|
1.13059e-05
|
|
|
KCS
|
[NCBI]
|
1.12735e-05
|
|
|
phosphoglycerate kinase 1 deficiency
|
[NCBI]
|
1.12735e-05
|
|
|
GS2
|
[NCBI]
|
1.12735e-05
|
|
|
bietti crystalline corneoretinal dystrophy
|
[NCBI]
|
1.12735e-05
|
|
|
LGMD1B
|
[NCBI]
|
1.12735e-05
|
|
|
fibromatosis, juvenile hyaline
|
[NCBI]
|
1.12735e-05
|
|
|
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus
|
[NCBI]
|
1.12735e-05
|
|
|
ABL
|
[NCBI]
|
1.12489e-05
|
|
|
ILK
|
[NCBI]
|
1.10307e-05
|
|
|
SPHK1
|
[NCBI]
|
1.06538e-05
|
|
|
TPM3
|
[NCBI]
|
1.06538e-05
|
|
|
ALPL
|
[NCBI]
|
1.06538e-05
|
|
|
CYP19A1
|
[NCBI]
|
1.05536e-05
|
|
|
B4GALT7
|
[NCBI]
|
1.04143e-05
|
|
|
LIN28
|
[NCBI]
|
1.04143e-05
|
|
|
UNG2
|
[NCBI]
|
1.04143e-05
|
|
|
CSRP3
|
[NCBI]
|
1.04143e-05
|
|
|
PHGDH
|
[NCBI]
|
1.04143e-05
|
|
|
AARS
|
[NCBI]
|
1.04143e-05
|
|
|
MYBBP1A
|
[NCBI]
|
1.04143e-05
|
|
|
ARPC4
|
[NCBI]
|
1.04143e-05
|
|
|
GTF2H5
|
[NCBI]
|
1.04143e-05
|
|
|
HYAL1
|
[NCBI]
|
1.04143e-05
|
|
|
CLN2
|
[NCBI]
|
1.04143e-05
|
|
|
ETFA
|
[NCBI]
|
1.04143e-05
|
|
|
ACAA1
|
[NCBI]
|
1.04143e-05
|
|
|
RHOG
|
[NCBI]
|
1.04143e-05
|
|
|
NEK3
|
[NCBI]
|
1.04143e-05
|
|
|
GCS1
|
[NCBI]
|
1.04143e-05
|
|
|
CITED1
|
[NCBI]
|
1.04143e-05
|
|
|
SCARB2
|
[NCBI]
|
1.04143e-05
|
|
|
NDUFV1
|
[NCBI]
|
1.04143e-05
|
|
|
NEUROD2
|
[NCBI]
|
1.04143e-05
|
|
|
BNIP3
|
[NCBI]
|
1.04143e-05
|
|
|
PUS1
|
[NCBI]
|
1.04143e-05
|
|
|
TLR8
|
[NCBI]
|
1.04143e-05
|
|
|
TRIM37
|
[NCBI]
|
1.04143e-05
|
|
|
proline-, glutamic acid-, and leucine-rich protein 1
|
[NCBI]
|
1.04143e-05
|
|
|
CPEB1
|
[NCBI]
|
1.04143e-05
|
|
|
MPDU1
|
[NCBI]
|
1.04143e-05
|
|
|
ca(2+)-promoted ras inactivator
|
[NCBI]
|
1.04143e-05
|
|
|
PMAIP1
|
[NCBI]
|
1.04143e-05
|
|
|
CSNK1E
|
[NCBI]
|
1.04143e-05
|
|
|
CEP2
|
[NCBI]
|
1.04143e-05
|
|
|
ATXN10
|
[NCBI]
|
1.04143e-05
|
|
|
rac- and cdc42-specific guanine nucleotide exchange factor
|
[NCBI]
|
1.04143e-05
|
|
|
MINPP1
|
[NCBI]
|
1.04143e-05
|
|
|
CXCL3
|
[NCBI]
|
1.04143e-05
|
|
|
ALDH4A1
|
[NCBI]
|
1.04143e-05
|
|
|
LIMS1
|
[NCBI]
|
1.04143e-05
|
|
|
CYFIP1
|
[NCBI]
|
1.04143e-05
|
|
|
SNAP29
|
[NCBI]
|
1.04143e-05
|
|
|
ADAMTS1
|
[NCBI]
|
1.04143e-05
|
|
|
RPE
|
[NCBI]
|
1.04143e-05
|
|
|
KLF12
|
[NCBI]
|
1.04143e-05
|
|
|
RFXANK
|
[NCBI]
|
1.04143e-05
|
|
|
TRIOBP
|
[NCBI]
|
1.04143e-05
|
|
|
XYLT1
|
[NCBI]
|
1.04143e-05
|
|
|
RAE1
|
[NCBI]
|
1.04143e-05
|
|
|
DPAGT1
|
[NCBI]
|
1.04143e-05
|
|
|
RASGRP1
|
[NCBI]
|
1.04143e-05
|
|
|
PAWR
|
[NCBI]
|
1.04143e-05
|
|
|
MTHFD2
|
[NCBI]
|
1.04143e-05
|
|
|
CKS1B
|
[NCBI]
|
1.04143e-05
|
|
|
ELAVL1
|
[NCBI]
|
1.04143e-05
|
|
|
PYCS
|
[NCBI]
|
1.04143e-05
|
|
|
STARD13
|
[NCBI]
|
1.04143e-05
|
|
|
FAP
|
[NCBI]
|
1.04143e-05
|
|
|
EIF3A
|
[NCBI]
|
1.04143e-05
|
|
|
SYBL1
|
[NCBI]
|
1.04143e-05
|
|
|
COIL
|
[NCBI]
|
1.04143e-05
|
|
|
ARPC3
|
[NCBI]
|
1.04143e-05
|
|
|
MNT
|
[NCBI]
|
1.04143e-05
|
|
|
JUND
|
[NCBI]
|
1.04143e-05
|
|
|
ARPC1B
|
[NCBI]
|
1.04143e-05
|
|
|
AP2M1
|
[NCBI]
|
1.04143e-05
|
|
|
GABRB1
|
[NCBI]
|
1.04143e-05
|
|
|
WAPAL
|
[NCBI]
|
1.04143e-05
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
1.02645e-05
|
|
|
PEDF
|
[NCBI]
|
1.02393e-05
|
|
|
HIF1A
|
[NCBI]
|
1.01999e-05
|
|
|
DMD
|
[NCBI]
|
1.01886e-05
|
|
|
ADM
|
[NCBI]
|
9.99434e-06
|
|
|
H2AFX
|
[NCBI]
|
9.97631e-06
|
|
|
tay-sachs disease, ab variant
|
[NCBI]
|
9.97631e-06
|
|
|
LGALS3
|
[NCBI]
|
9.97631e-06
|
|
|
CTSB
|
[NCBI]
|
9.97631e-06
|
|
|
SREBF1
|
[NCBI]
|
9.97631e-06
|
|
|
RPS6KA1
|
[NCBI]
|
9.97631e-06
|
|
|
PDGFRA
|
[NCBI]
|
9.97631e-06
|
|
|
GCDH
|
[NCBI]
|
9.97631e-06
|
|
|
IL17A
|
[NCBI]
|
9.97631e-06
|
|
|
EBP
|
[NCBI]
|
9.97631e-06
|
|
|
CHM
|
[NCBI]
|
9.93118e-06
|
|
|
ACP5
|
[NCBI]
|
9.72626e-06
|
|
|
HPS
|
[NCBI]
|
9.6899e-06
|
|
|
PF4
|
[NCBI]
|
9.6756e-06
|
|
|
JAK2
|
[NCBI]
|
9.53541e-06
|
|
|
STAT5A
|
[NCBI]
|
9.47276e-06
|
|
|
ADRP
|
[NCBI]
|
9.3752e-06
|
|
|
CASP8
|
[NCBI]
|
9.34891e-06
|
|
|
TERF2
|
[NCBI]
|
9.34891e-06
|
|
|
DBI
|
[NCBI]
|
9.33081e-06
|
|
|
DBA
|
[NCBI]
|
9.30186e-06
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
9.24693e-06
|
|
|
NPS
|
[NCBI]
|
9.24693e-06
|
|
|
opitz syndrome
|
[NCBI]
|
9.04988e-06
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
9.04988e-06
|
|
|
gaucher disease, type ii
|
[NCBI]
|
9.04988e-06
|
|
|
homocysteinemia
|
[NCBI]
|
9.04988e-06
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
9.04988e-06
|
|
|
leiomyomatosis and renal cell cancer, hereditary
|
[NCBI]
|
9.04988e-06
|
|
|
complement factor h deficiency
|
[NCBI]
|
9.04988e-06
|
|
|
minicore myopathy with external ophthalmoplegia
|
[NCBI]
|
9.04988e-06
|
|
|
ERBB2
|
[NCBI]
|
8.98768e-06
|
|
|
methemoglobinemia due to deficiency of methemoglobin reductase
|
[NCBI]
|
8.98768e-06
|
|
|
OPA1
|
[NCBI]
|
8.92265e-06
|
|
|
ABP1
|
[NCBI]
|
8.89618e-06
|
|
|
AKR1B1
|
[NCBI]
|
8.79397e-06
|
|
|
RAD51L3
|
[NCBI]
|
8.79148e-06
|
|
|
SLC20A1
|
[NCBI]
|
8.79148e-06
|
|
|
ARPC2
|
[NCBI]
|
8.79148e-06
|
|
|
STC2
|
[NCBI]
|
8.79148e-06
|
|
|
DHCR24
|
[NCBI]
|
8.79148e-06
|
|
|
ARAF1
|
[NCBI]
|
8.79148e-06
|
|
|
SLC25A3
|
[NCBI]
|
8.79148e-06
|
|
|
IL17F
|
[NCBI]
|
8.79148e-06
|
|
|
PDGFD
|
[NCBI]
|
8.79148e-06
|
|
|
ADAM12
|
[NCBI]
|
8.79148e-06
|
|
|
COQ2
|
[NCBI]
|
8.79148e-06
|
|
|
PEX14
|
[NCBI]
|
8.79148e-06
|
|
|
MCAM
|
[NCBI]
|
8.79148e-06
|
|
|
UHRF1
|
[NCBI]
|
8.79148e-06
|
|
|
rapamycin-insensitive companion of mtor
|
[NCBI]
|
8.79148e-06
|
|
|
BAD
|
[NCBI]
|
8.79148e-06
|
|
|
jtv1 gene
|
[NCBI]
|
8.79148e-06
|
|
|
PTGES3
|
[NCBI]
|
8.79148e-06
|
|
|
CTBP2
|
[NCBI]
|
8.79148e-06
|
|
|
PDGFC
|
[NCBI]
|
8.79148e-06
|
|
|
NOL1
|
[NCBI]
|
8.79148e-06
|
|
|
CS
|
[NCBI]
|
8.79148e-06
|
|
|
RORB
|
[NCBI]
|
8.79148e-06
|
|
|
RING1
|
[NCBI]
|
8.79148e-06
|
|
|
ACTR3
|
[NCBI]
|
8.79148e-06
|
|
|
CSK
|
[NCBI]
|
8.79148e-06
|
|
|
IL17RA
|
[NCBI]
|
8.79148e-06
|
|
|
TRIM29
|
[NCBI]
|
8.79148e-06
|
|
|
HTRA2
|
[NCBI]
|
8.79148e-06
|
|
|
MCCC1
|
[NCBI]
|
8.79148e-06
|
|
|
CIZ1
|
[NCBI]
|
8.79148e-06
|
|
|
ZNF217
|
[NCBI]
|
8.79148e-06
|
|
|
BLVRA
|
[NCBI]
|
8.79148e-06
|
|
|
SAI1
|
[NCBI]
|
8.79148e-06
|
|
|
HAO1
|
[NCBI]
|
8.79148e-06
|
|
|
BCAP31
|
[NCBI]
|
8.79148e-06
|
|
|
PMS1
|
[NCBI]
|
8.79148e-06
|
|
|
SLC27A2
|
[NCBI]
|
8.79148e-06
|
|
|
FUCA2
|
[NCBI]
|
8.79148e-06
|
|
|
ATE1
|
[NCBI]
|
8.79148e-06
|
|
|
LMF1
|
[NCBI]
|
8.79148e-06
|
|
|
CASP7
|
[NCBI]
|
8.79148e-06
|
|
|
AKT3
|
[NCBI]
|
8.79148e-06
|
|
|
IGFBP7
|
[NCBI]
|
8.79148e-06
|
|
|
DLAT
|
[NCBI]
|
8.79148e-06
|
|
|
DPT
|
[NCBI]
|
8.79148e-06
|
|
|
SLC35C1
|
[NCBI]
|
8.79148e-06
|
|
|
IL11
|
[NCBI]
|
8.79148e-06
|
|
|
MTF1
|
[NCBI]
|
8.79148e-06
|
|
|
SLC27A4
|
[NCBI]
|
8.79148e-06
|
|
|
ZFP36L1
|
[NCBI]
|
8.79148e-06
|
|
|
HAS3
|
[NCBI]
|
8.79148e-06
|
|
|
USP6NL
|
[NCBI]
|
8.79148e-06
|
|
|
GFRA3
|
[NCBI]
|
8.79148e-06
|
|
|
PIAS4
|
[NCBI]
|
8.79148e-06
|
|
|
PHF9
|
[NCBI]
|
8.79148e-06
|
|
|
LDHA
|
[NCBI]
|
8.76617e-06
|
|
|
CARM1
|
[NCBI]
|
8.76617e-06
|
|
|
ALCAM
|
[NCBI]
|
8.76617e-06
|
|
|
APRT
|
[NCBI]
|
8.75709e-06
|
|
|
PTK2B
|
[NCBI]
|
8.67831e-06
|
|
|
HRAS
|
[NCBI]
|
8.61555e-06
|
|
|
TCOF
|
[NCBI]
|
8.57768e-06
|
|
|
hypertension, essential
|
[NCBI]
|
8.57768e-06
|
|
|
GHR
|
[NCBI]
|
8.41986e-06
|
|
|
PMD
|
[NCBI]
|
8.2524e-06
|
|
|
CHRNE
|
[NCBI]
|
8.2235e-06
|
|
|
C3
|
[NCBI]
|
8.2235e-06
|
|
|
ATR
|
[NCBI]
|
8.2235e-06
|
|
|
HMBS
|
[NCBI]
|
8.21921e-06
|
|
|
RBP1
|
[NCBI]
|
8.21106e-06
|
|
|
DSPP
|
[NCBI]
|
8.14625e-06
|
|
|
KDR
|
[NCBI]
|
8.07317e-06
|
|
|
TLR3
|
[NCBI]
|
7.88192e-06
|
|
|
MAPK8
|
[NCBI]
|
7.71697e-06
|
|
|
SFRP1
|
[NCBI]
|
7.71697e-06
|
|
|
CLOCK
|
[NCBI]
|
7.71697e-06
|
|
|
RECQL3
|
[NCBI]
|
7.71697e-06
|
|
|
TLR2
|
[NCBI]
|
7.63897e-06
|
|
|
CENPB
|
[NCBI]
|
7.53818e-06
|
|
|
SMC3
|
[NCBI]
|
7.53818e-06
|
|
|
SLC29A2
|
[NCBI]
|
7.53818e-06
|
|
|
ACAT2
|
[NCBI]
|
7.53818e-06
|
|
|
IL13RA2
|
[NCBI]
|
7.53818e-06
|
|
|
CKAP2
|
[NCBI]
|
7.53818e-06
|
|
|
PLEKHC1
|
[NCBI]
|
7.53818e-06
|
|
|
TEGT
|
[NCBI]
|
7.53818e-06
|
|
|
PHB2
|
[NCBI]
|
7.53818e-06
|
|
|
HAS1
|
[NCBI]
|
7.53818e-06
|
|
|
BAG1
|
[NCBI]
|
7.53818e-06
|
|
|
JAG2
|
[NCBI]
|
7.53818e-06
|
|
|
SRD5A2
|
[NCBI]
|
7.53818e-06
|
|
|
STUB1
|
[NCBI]
|
7.53818e-06
|
|
|
IL11RA
|
[NCBI]
|
7.53818e-06
|
|
|
VAMP8
|
[NCBI]
|
7.53818e-06
|
|
|
SUMF1
|
[NCBI]
|
7.53818e-06
|
|
|
NFIA
|
[NCBI]
|
7.53818e-06
|
|
|
RAB8A
|
[NCBI]
|
7.53818e-06
|
|
|
S100A4
|
[NCBI]
|
7.53818e-06
|
|
|
DPYSL2
|
[NCBI]
|
7.53818e-06
|
|
|
TACR2
|
[NCBI]
|
7.53818e-06
|
|
|
GNA13
|
[NCBI]
|
7.53818e-06
|
|
|
thyrotropin-releasing hormone deficiency
|
[NCBI]
|
7.53818e-06
|
|
|
MCRS1
|
[NCBI]
|
7.53818e-06
|
|
|
BIK
|
[NCBI]
|
7.53818e-06
|
|
|
KHSRP
|
[NCBI]
|
7.53818e-06
|
|
|
ABCG1
|
[NCBI]
|
7.53818e-06
|
|
|
PXF
|
[NCBI]
|
7.53818e-06
|
|
|
SLC9A1
|
[NCBI]
|
7.53818e-06
|
|
|
TICAM1
|
[NCBI]
|
7.53818e-06
|
|
|
RNF2
|
[NCBI]
|
7.53818e-06
|
|
|
HSPA6
|
[NCBI]
|
7.53818e-06
|
|
|
TOP3A
|
[NCBI]
|
7.53818e-06
|
|
|
switch-associated protein 70
|
[NCBI]
|
7.53818e-06
|
|
|
BACE2
|
[NCBI]
|
7.53818e-06
|
|
|
DIDO1
|
[NCBI]
|
7.53818e-06
|
|
|
PTPRE
|
[NCBI]
|
7.53818e-06
|
|
|
FUBP1
|
[NCBI]
|
7.53818e-06
|
|
|
SLC9A3R1
|
[NCBI]
|
7.53818e-06
|
|
|
DPYS
|
[NCBI]
|
7.53818e-06
|
|
|
THBS2
|
[NCBI]
|
7.53818e-06
|
|
|
EDG5
|
[NCBI]
|
7.53818e-06
|
|
|
MPG
|
[NCBI]
|
7.53818e-06
|
|
|
CUGBP2
|
[NCBI]
|
7.53818e-06
|
|
|
LAP3
|
[NCBI]
|
7.53818e-06
|
|
|
BAT1
|
[NCBI]
|
7.53818e-06
|
|
|
NDUFS1
|
[NCBI]
|
7.53818e-06
|
|
|
ANPEP
|
[NCBI]
|
7.53818e-06
|
|
|
S100A11
|
[NCBI]
|
7.53818e-06
|
|
|
CDC25B
|
[NCBI]
|
7.53818e-06
|
|
|
SMC1A
|
[NCBI]
|
7.53818e-06
|
|
|
MAP6
|
[NCBI]
|
7.53818e-06
|
|
|
CHAD
|
[NCBI]
|
7.53818e-06
|
|
|
SART3
|
[NCBI]
|
7.53818e-06
|
|
|
SDC4
|
[NCBI]
|
7.53818e-06
|
|
|
EEF1A2
|
[NCBI]
|
7.53818e-06
|
|
|
SOS1
|
[NCBI]
|
7.53818e-06
|
|
|
BMP4
|
[NCBI]
|
7.52661e-06
|
|
|
PSORS1
|
[NCBI]
|
7.28711e-06
|
|
|
LDHB
|
[NCBI]
|
7.24322e-06
|
|
|
MAP3K7
|
[NCBI]
|
7.24322e-06
|
|
|
MLH1
|
[NCBI]
|
7.24322e-06
|
|
|
PTX3
|
[NCBI]
|
7.24322e-06
|
|
|
buschke-ollendorff syndrome
|
[NCBI]
|
7.22261e-06
|
|
|
ISS
|
[NCBI]
|
7.22261e-06
|
|
|
sea-blue histiocyte disease
|
[NCBI]
|
7.22261e-06
|
|
|
periodic fever, familial, autosomal dominant
|
[NCBI]
|
7.22261e-06
|
|
|
PALS
|
[NCBI]
|
7.22261e-06
|
|
|
USH3
|
[NCBI]
|
7.22261e-06
|
|
|
BPP
|
[NCBI]
|
7.22261e-06
|
|
|
PRNP
|
[NCBI]
|
6.98841e-06
|
|
|
THRB
|
[NCBI]
|
6.96013e-06
|
|
|
F2R
|
[NCBI]
|
6.89506e-06
|
|
|
RBS
|
[NCBI]
|
6.84932e-06
|
|
|
DCK
|
[NCBI]
|
6.80914e-06
|
|
|
CACNA1C
|
[NCBI]
|
6.79932e-06
|
|
|
ACH
|
[NCBI]
|
6.73882e-06
|
|
|
COMP
|
[NCBI]
|
6.69262e-06
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
6.66738e-06
|
|
|
SCIDX1
|
[NCBI]
|
6.66738e-06
|
|
|
NFKB1
|
[NCBI]
|
6.66566e-06
|
|
|
ARF3
|
[NCBI]
|
6.52907e-06
|
|
|
CTCFL
|
[NCBI]
|
6.52907e-06
|
|
|
CLSPN
|
[NCBI]
|
6.52907e-06
|
|
|
EGR3
|
[NCBI]
|
6.52907e-06
|
|
|
RFX5
|
[NCBI]
|
6.52907e-06
|
|
|
LAMP1
|
[NCBI]
|
6.52907e-06
|
|
|
CASP9
|
[NCBI]
|
6.52907e-06
|
|
|
CSRP2
|
[NCBI]
|
6.52907e-06
|
|
|
DUSP1
|
[NCBI]
|
6.52907e-06
|
|
|
CCL7
|
[NCBI]
|
6.52907e-06
|
|
|
ABCD2
|
[NCBI]
|
6.52907e-06
|
|
|
GPR77
|
[NCBI]
|
6.52907e-06
|
|
|
RPL7
|
[NCBI]
|
6.52907e-06
|
|
|
CTNNA2
|
[NCBI]
|
6.52907e-06
|
|
|
SGCE
|
[NCBI]
|
6.52907e-06
|
|
|
SCO2
|
[NCBI]
|
6.52907e-06
|
|
|
SLC30A4
|
[NCBI]
|
6.52907e-06
|
|
|
SEPN1
|
[NCBI]
|
6.52907e-06
|
|
|
ACTR2
|
[NCBI]
|
6.52907e-06
|
|
|
SUFU
|
[NCBI]
|
6.52907e-06
|
|
|
DUT
|
[NCBI]
|
6.52907e-06
|
|
|
SLC19A2
|
[NCBI]
|
6.52907e-06
|
|
|
NSDHL
|
[NCBI]
|
6.52907e-06
|
|
|
SLC9A3R2
|
[NCBI]
|
6.52907e-06
|
|
|
M6PR
|
[NCBI]
|
6.52907e-06
|
|
|
BMP6
|
[NCBI]
|
6.52907e-06
|
|
|
TIMP2
|
[NCBI]
|
6.52907e-06
|
|
|
MAP2K4
|
[NCBI]
|
6.52907e-06
|
|
|
CUL3
|
[NCBI]
|
6.52907e-06
|
|
|
FXR2
|
[NCBI]
|
6.52907e-06
|
|
|
GFRA1
|
[NCBI]
|
6.52907e-06
|
|
|
CD1B
|
[NCBI]
|
6.52907e-06
|
|
|
PPP2CA
|
[NCBI]
|
6.52907e-06
|
|
|
SECISBP2
|
[NCBI]
|
6.52907e-06
|
|
|
RPA1
|
[NCBI]
|
6.52907e-06
|
|
|
TBX2
|
[NCBI]
|
6.52907e-06
|
|
|
ADRB1
|
[NCBI]
|
6.52907e-06
|
|
|
TICAM2
|
[NCBI]
|
6.52907e-06
|
|
|
EMILIN1
|
[NCBI]
|
6.52907e-06
|
|
|
CALR
|
[NCBI]
|
6.52907e-06
|
|
|
LUM
|
[NCBI]
|
6.52907e-06
|
|
|
EDG3
|
[NCBI]
|
6.52907e-06
|
|
|
COPS5
|
[NCBI]
|
6.52907e-06
|
|
|
GCLC
|
[NCBI]
|
6.52907e-06
|
|
|
MBD4
|
[NCBI]
|
6.52907e-06
|
|
|
PTPNS1
|
[NCBI]
|
6.52907e-06
|
|
|
GTF2I
|
[NCBI]
|
6.52907e-06
|
|
|
FANCB
|
[NCBI]
|
6.52907e-06
|
|
|
LOXL1
|
[NCBI]
|
6.52907e-06
|
|
|
VRK1
|
[NCBI]
|
6.52907e-06
|
|
|
RPS3A
|
[NCBI]
|
6.52907e-06
|
|
|
HSPA5
|
[NCBI]
|
6.52907e-06
|
|
|
HMGCS2
|
[NCBI]
|
6.52907e-06
|
|
|
THRSP
|
[NCBI]
|
6.52907e-06
|
|
|
IL1R1
|
[NCBI]
|
6.52907e-06
|
|
|
HES1
|
[NCBI]
|
6.52907e-06
|
|
|
RAB5A
|
[NCBI]
|
6.52907e-06
|
|
|
BTD
|
[NCBI]
|
6.52907e-06
|
|
|
VDR
|
[NCBI]
|
6.45737e-06
|
|
|
VEGF
|
[NCBI]
|
6.44751e-06
|
|
|
GLA
|
[NCBI]
|
6.38273e-06
|
|
|
INPP5D
|
[NCBI]
|
6.38273e-06
|
|
|
TAF1
|
[NCBI]
|
6.38273e-06
|
|
|
PRKDC
|
[NCBI]
|
6.38273e-06
|
|
|
MYD88
|
[NCBI]
|
6.38273e-06
|
|
|
SP7
|
[NCBI]
|
6.38273e-06
|
|
|
MMP9
|
[NCBI]
|
6.38211e-06
|
|
|
NF1
|
[NCBI]
|
6.34589e-06
|
|
|
GSR
|
[NCBI]
|
6.10902e-06
|
|
|
campomelic dysplasia
|
[NCBI]
|
6.06584e-06
|
|
|
FGF4
|
[NCBI]
|
5.99121e-06
|
|
|
EMD
|
[NCBI]
|
5.99121e-06
|
|
|
E2F1
|
[NCBI]
|
5.99121e-06
|
|
|
HDAC2
|
[NCBI]
|
5.99121e-06
|
|
|
BRCA2
|
[NCBI]
|
5.84593e-06
|
|
|
BMP2
|
[NCBI]
|
5.80493e-06
|
|
|
hypophosphatasia, adult type
|
[NCBI]
|
5.71193e-06
|
|
|
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
[NCBI]
|
5.71193e-06
|
|
|
ACG2
|
[NCBI]
|
5.71193e-06
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
5.71193e-06
|
|
|
NSEP1
|
[NCBI]
|
5.69353e-06
|
|
|
TYK2
|
[NCBI]
|
5.69353e-06
|
|
|
CENPE
|
[NCBI]
|
5.69353e-06
|
|
|
TBCE
|
[NCBI]
|
5.69353e-06
|
|
|
DDB2
|
[NCBI]
|
5.69353e-06
|
|
|
CD74
|
[NCBI]
|
5.69353e-06
|
|
|
NT5C
|
[NCBI]
|
5.69353e-06
|
|
|
DUSP6
|
[NCBI]
|
5.69353e-06
|
|
|
DAPK1
|
[NCBI]
|
5.69353e-06
|
|
|
ADRA1B
|
[NCBI]
|
5.69353e-06
|
|
|
PIP5K1C
|
[NCBI]
|
5.69353e-06
|
|
|
BTG2
|
[NCBI]
|
5.69353e-06
|
|
|
CLDN14
|
[NCBI]
|
5.69353e-06
|
|
|
LIM2
|
[NCBI]
|
5.69353e-06
|
|
|
PGM2
|
[NCBI]
|
5.69353e-06
|
|
|
CSPG2
|
[NCBI]
|
5.69353e-06
|
|
|
TACR3
|
[NCBI]
|
5.69353e-06
|
|
|
SKP1A
|
[NCBI]
|
5.69353e-06
|
|
|
ROBO1
|
[NCBI]
|
5.69353e-06
|
|
|
BCL3
|
[NCBI]
|
5.69353e-06
|
|
|
VCL
|
[NCBI]
|
5.69353e-06
|
|
|
JAM1
|
[NCBI]
|
5.69353e-06
|
|
|
RPL5
|
[NCBI]
|
5.69353e-06
|
|
|
ANXA7
|
[NCBI]
|
5.69353e-06
|
|
|
CYP27A1
|
[NCBI]
|
5.69353e-06
|
|
|
IGFBP5
|
[NCBI]
|
5.69353e-06
|
|
|
CDC18L
|
[NCBI]
|
5.69353e-06
|
|
|
LEFTY2
|
[NCBI]
|
5.69353e-06
|
|
|
PRMT1
|
[NCBI]
|
5.69353e-06
|
|
|
DGUOK
|
[NCBI]
|
5.69353e-06
|
|
|
G22P1
|
[NCBI]
|
5.69353e-06
|
|
|
GPD2
|
[NCBI]
|
5.69353e-06
|
|
|
CCS
|
[NCBI]
|
5.69353e-06
|
|
|
SEMA5A
|
[NCBI]
|
5.69353e-06
|
|
|
UBQLN1
|
[NCBI]
|
5.69353e-06
|
|
|
PDCD5
|
[NCBI]
|
5.69353e-06
|
|
|
HOXD3
|
[NCBI]
|
5.69353e-06
|
|
|
FCER2
|
[NCBI]
|
5.69353e-06
|
|
|
NEUROG1
|
[NCBI]
|
5.69353e-06
|
|
|
PPM1D
|
[NCBI]
|
5.69353e-06
|
|
|
FSTL1
|
[NCBI]
|
5.69353e-06
|
|
|
SDHA
|
[NCBI]
|
5.69353e-06
|
|
|
CBFB
|
[NCBI]
|
5.69353e-06
|
|
|
BCS1L
|
[NCBI]
|
5.69353e-06
|
|
|
HYAL2
|
[NCBI]
|
5.69353e-06
|
|
|
LFNG
|
[NCBI]
|
5.62279e-06
|
|
|
CCND1
|
[NCBI]
|
5.60424e-06
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
5.59521e-06
|
|
|
CFH
|
[NCBI]
|
5.59243e-06
|
|
|
TS
|
[NCBI]
|
5.50784e-06
|
|
|
ABCG2
|
[NCBI]
|
5.48683e-06
|
|
|
down syndrome
|
[NCBI]
|
5.48345e-06
|
|
|
GCPS
|
[NCBI]
|
5.48345e-06
|
|
|
MUC1
|
[NCBI]
|
5.45215e-06
|
|
|
GJB2
|
[NCBI]
|
5.43035e-06
|
|
|
FRAP1
|
[NCBI]
|
5.38277e-06
|
|
|
PIGR
|
[NCBI]
|
5.30477e-06
|
|
|
CES1
|
[NCBI]
|
5.27572e-06
|
|
|
TLR7
|
[NCBI]
|
5.27572e-06
|
|
|
TSC1
|
[NCBI]
|
5.27572e-06
|
|
|
GAPDH
|
[NCBI]
|
5.22697e-06
|
|
|
SLC2A4
|
[NCBI]
|
5.09106e-06
|
|
|
F3
|
[NCBI]
|
5.07172e-06
|
|
|
glutathionuria
|
[NCBI]
|
4.98776e-06
|
|
|
ACTG1
|
[NCBI]
|
4.98776e-06
|
|
|
TNFAIP3
|
[NCBI]
|
4.98776e-06
|
|
|
WWOX
|
[NCBI]
|
4.98776e-06
|
|
|
GCLM
|
[NCBI]
|
4.98776e-06
|
|
|
C1NH
|
[NCBI]
|
4.98776e-06
|
|
|
CCND2
|
[NCBI]
|
4.98776e-06
|
|
|
CBX1
|
[NCBI]
|
4.98776e-06
|
|
|
PXN
|
[NCBI]
|
4.98776e-06
|
|
|
PKP2
|
[NCBI]
|
4.98776e-06
|
|
|
RPS6KB1
|
[NCBI]
|
4.98776e-06
|
|
|
WNT4
|
[NCBI]
|
4.98776e-06
|
|
|
ARSE
|
[NCBI]
|
4.98776e-06
|
|
|
ABCA2
|
[NCBI]
|
4.98776e-06
|
|
|
GALE
|
[NCBI]
|
4.98776e-06
|
|
|
KRT7
|
[NCBI]
|
4.98776e-06
|
|
|
CENPC1
|
[NCBI]
|
4.98776e-06
|
|
|
MAPK6
|
[NCBI]
|
4.98776e-06
|
|
|
IDH2
|
[NCBI]
|
4.98776e-06
|
|
|
FADD
|
[NCBI]
|
4.98776e-06
|
|
|
OAS1
|
[NCBI]
|
4.98776e-06
|
|
|
IL1RL1
|
[NCBI]
|
4.98776e-06
|
|
|
BCL2L1
|
[NCBI]
|
4.98776e-06
|
|
|
PARP4
|
[NCBI]
|
4.98776e-06
|
|
|
GSS
|
[NCBI]
|
4.98776e-06
|
|
|
RAB7
|
[NCBI]
|
4.98776e-06
|
|
|
CCNB1
|
[NCBI]
|
4.98776e-06
|
|
|
MYF5
|
[NCBI]
|
4.98776e-06
|
|
|
LARGE
|
[NCBI]
|
4.98776e-06
|
|
|
FKHL16
|
[NCBI]
|
4.98776e-06
|
|
|
PLCG1
|
[NCBI]
|
4.98776e-06
|
|
|
MTTI
|
[NCBI]
|
4.98776e-06
|
|
|
SLC34A1
|
[NCBI]
|
4.98776e-06
|
|
|
CHEK1
|
[NCBI]
|
4.98776e-06
|
|
|
SFN
|
[NCBI]
|
4.98776e-06
|
|
|
TPO
|
[NCBI]
|
4.96963e-06
|
|
|
BCR
|
[NCBI]
|
4.93594e-06
|
|
|
BRRS
|
[NCBI]
|
4.92124e-06
|
|
|
CLN3
|
[NCBI]
|
4.92124e-06
|
|
|
porphyria variegata
|
[NCBI]
|
4.92124e-06
|
|
|
hemophilia a
|
[NCBI]
|
4.88565e-06
|
|
|
IL4
|
[NCBI]
|
4.8097e-06
|
|
|
PLG
|
[NCBI]
|
4.72977e-06
|
|
|
MCP
|
[NCBI]
|
4.685e-06
|
|
|
GNAS
|
[NCBI]
|
4.66682e-06
|
|
|
CRY1
|
[NCBI]
|
4.6396e-06
|
|
|
KLRK1
|
[NCBI]
|
4.6396e-06
|
|
|
IKBKG
|
[NCBI]
|
4.6396e-06
|
|
|
CFLAR
|
[NCBI]
|
4.6396e-06
|
|
|
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to
|
[NCBI]
|
4.46003e-06
|
|
|
paget disease, juvenile
|
[NCBI]
|
4.46003e-06
|
|
|
CMT4A
|
[NCBI]
|
4.46003e-06
|
|
|
USH1C
|
[NCBI]
|
4.46003e-06
|
|
|
CMT2A1
|
[NCBI]
|
4.46003e-06
|
|
|
seckel syndrome 1
|
[NCBI]
|
4.46003e-06
|
|
|
FED
|
[NCBI]
|
4.46003e-06
|
|
|
HHS
|
[NCBI]
|
4.46003e-06
|
|
|
succinic semialdehyde dehydrogenase deficiency
|
[NCBI]
|
4.46003e-06
|
|
|
HSAN2
|
[NCBI]
|
4.46003e-06
|
|
|
kniest dysplasia
|
[NCBI]
|
4.46003e-06
|
|
|
SCCMS
|
[NCBI]
|
4.46003e-06
|
|
|
bladder cancer
|
[NCBI]
|
4.46003e-06
|
|
|
LPI
|
[NCBI]
|
4.4499e-06
|
|
|
NCOR1
|
[NCBI]
|
4.38272e-06
|
|
|
SFTPC
|
[NCBI]
|
4.38272e-06
|
|
|
SLC17A5
|
[NCBI]
|
4.38272e-06
|
|
|
ERN1
|
[NCBI]
|
4.38272e-06
|
|
|
DPP4
|
[NCBI]
|
4.38272e-06
|
|
|
EDG1
|
[NCBI]
|
4.38272e-06
|
|
|
BCAR1
|
[NCBI]
|
4.38272e-06
|
|
|
CCL5
|
[NCBI]
|
4.38272e-06
|
|
|
CDC25A
|
[NCBI]
|
4.38272e-06
|
|
|
LMNB1
|
[NCBI]
|
4.38272e-06
|
|
|
FXR1
|
[NCBI]
|
4.38272e-06
|
|
|
CDKN2B
|
[NCBI]
|
4.38272e-06
|
|
|
PDCD4
|
[NCBI]
|
4.38272e-06
|
|
|
METAP2
|
[NCBI]
|
4.38272e-06
|
|
|
AMFR
|
[NCBI]
|
4.38272e-06
|
|
|
SPTLC1
|
[NCBI]
|
4.38272e-06
|
|
|
RANBP2
|
[NCBI]
|
4.38272e-06
|
|
|
SFRP4
|
[NCBI]
|
4.38272e-06
|
|
|
GPX4
|
[NCBI]
|
4.38272e-06
|
|
|
OGN
|
[NCBI]
|
4.38272e-06
|
|
|
SMAD7
|
[NCBI]
|
4.38272e-06
|
|
|
POT1
|
[NCBI]
|
4.38272e-06
|
|
|
RAPSN
|
[NCBI]
|
4.38272e-06
|
|
|
PPBP
|
[NCBI]
|
4.38272e-06
|
|
|
YY1
|
[NCBI]
|
4.38272e-06
|
|
|
NFE2L2
|
[NCBI]
|
4.38272e-06
|
|
|
PICK1
|
[NCBI]
|
4.38272e-06
|
|
|
NFAT5
|
[NCBI]
|
4.38272e-06
|
|
|
RORA
|
[NCBI]
|
4.38272e-06
|
|
|
MIRN155
|
[NCBI]
|
4.38272e-06
|
|
|
STAT1
|
[NCBI]
|
4.37715e-06
|
|
|
REN
|
[NCBI]
|
4.3479e-06
|
|
|
CDK6
|
[NCBI]
|
4.3479e-06
|
|
|
RPS6KA3
|
[NCBI]
|
4.3479e-06
|
|
|
NSF
|
[NCBI]
|
4.32703e-06
|
|
|
PLAUR
|
[NCBI]
|
4.30066e-06
|
|
|
CDC2
|
[NCBI]
|
4.25239e-06
|
|
|
KITLG
|
[NCBI]
|
4.18317e-06
|
|
|
PPARA
|
[NCBI]
|
4.08547e-06
|
|
|
CDH1
|
[NCBI]
|
4.07224e-06
|
|
|
PSIP1
|
[NCBI]
|
4.07224e-06
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
4.07224e-06
|
|
|
GPX1
|
[NCBI]
|
4.07224e-06
|
|
|
FOXO1A
|
[NCBI]
|
4.07224e-06
|
|
|
PPIA
|
[NCBI]
|
3.97382e-06
|
|
|
SLC1A5
|
[NCBI]
|
3.85815e-06
|
|
|
ENAH
|
[NCBI]
|
3.85815e-06
|
|
|
HMGA1
|
[NCBI]
|
3.85815e-06
|
|
|
DSC1
|
[NCBI]
|
3.85815e-06
|
|
|
TRPA1
|
[NCBI]
|
3.85815e-06
|
|
|
CKM
|
[NCBI]
|
3.85815e-06
|
|
|
MEST
|
[NCBI]
|
3.85815e-06
|
|
|
CRP
|
[NCBI]
|
3.85815e-06
|
|
|
SGK
|
[NCBI]
|
3.85815e-06
|
|
|
EZH2
|
[NCBI]
|
3.85815e-06
|
|
|
PYCARD
|
[NCBI]
|
3.85815e-06
|
|
|
B4GALT1
|
[NCBI]
|
3.85815e-06
|
|
|
MCPH1
|
[NCBI]
|
3.85815e-06
|
|
|
DAP3
|
[NCBI]
|
3.85815e-06
|
|
|
HPS1
|
[NCBI]
|
3.85815e-06
|
|
|
PMS2
|
[NCBI]
|
3.85815e-06
|
|
|
farber lipogranulomatosis
|
[NCBI]
|
3.85815e-06
|
|
|
TIMM8A
|
[NCBI]
|
3.85815e-06
|
|
|
XG
|
[NCBI]
|
3.85815e-06
|
|
|
TSHB
|
[NCBI]
|
3.85815e-06
|
|
|
IGLC1
|
[NCBI]
|
3.85815e-06
|
|
|
FLNB
|
[NCBI]
|
3.85815e-06
|
|
|
DHCR7
|
[NCBI]
|
3.85815e-06
|
|
|
CTSG
|
[NCBI]
|
3.85815e-06
|
|
|
CXCL2
|
[NCBI]
|
3.85815e-06
|
|
|
FMOD
|
[NCBI]
|
3.85815e-06
|
|
|
HTR2A
|
[NCBI]
|
3.85815e-06
|
|
|
GNB3
|
[NCBI]
|
3.85815e-06
|
|
|
COL5A1
|
[NCBI]
|
3.85815e-06
|
|
|
PKM2
|
[NCBI]
|
3.85815e-06
|
|
|
LAMB3
|
[NCBI]
|
3.85815e-06
|
|
|
IRF4
|
[NCBI]
|
3.85815e-06
|
|
|
CCND3
|
[NCBI]
|
3.85815e-06
|
|
|
HADH
|
[NCBI]
|
3.85815e-06
|
|
|
MDH1
|
[NCBI]
|
3.85815e-06
|
|
|
MBTPS2
|
[NCBI]
|
3.85815e-06
|
|
|
CCL22
|
[NCBI]
|
3.85786e-06
|
|
|
BWS
|
[NCBI]
|
3.82479e-06
|
|
|
KRAS
|
[NCBI]
|
3.81158e-06
|
|
|
IL8
|
[NCBI]
|
3.81158e-06
|
|
|
PGM1
|
[NCBI]
|
3.81158e-06
|
|
|
PRG4
|
[NCBI]
|
3.81158e-06
|
|
|
MTCYB
|
[NCBI]
|
3.81158e-06
|
|
|
breast cancer
|
[NCBI]
|
3.74402e-06
|
|
|
LAT
|
[NCBI]
|
3.62871e-06
|
|
|
PRLR
|
[NCBI]
|
3.62871e-06
|
|
|
BGLAP
|
[NCBI]
|
3.62375e-06
|
|
|
INCENP
|
[NCBI]
|
3.56501e-06
|
|
|
JAK1
|
[NCBI]
|
3.56501e-06
|
|
|
SCD
|
[NCBI]
|
3.51558e-06
|
|
|
DFSP
|
[NCBI]
|
3.45054e-06
|
|
|
PLTP
|
[NCBI]
|
3.44007e-06
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
3.42362e-06
|
|
|
dent disease 1
|
[NCBI]
|
3.42362e-06
|
|
|
SMA2
|
[NCBI]
|
3.42362e-06
|
|
|
CDG2C
|
[NCBI]
|
3.42362e-06
|
|
|
CRS1
|
[NCBI]
|
3.42362e-06
|
|
|
methionine adenosyltransferase deficiency
|
[NCBI]
|
3.42362e-06
|
|
|
LCA1
|
[NCBI]
|
3.42362e-06
|
|
|
pancreatic carcinoma
|
[NCBI]
|
3.42362e-06
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
3.42362e-06
|
|
|
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
[NCBI]
|
3.42362e-06
|
|
|
TRPV1
|
[NCBI]
|
3.40343e-06
|
|
|
virus-induced signaling adaptor
|
[NCBI]
|
3.39935e-06
|
|
|
CHST3
|
[NCBI]
|
3.39935e-06
|
|
|
UGDH
|
[NCBI]
|
3.39935e-06
|
|
|
CDC25C
|
[NCBI]
|
3.39935e-06
|
|
|
GNL3
|
[NCBI]
|
3.39935e-06
|
|
|
RASSF1
|
[NCBI]
|
3.39935e-06
|
|
|
DDX58
|
[NCBI]
|
3.39935e-06
|
|
|
MTP
|
[NCBI]
|
3.39935e-06
|
|
|
MCF2
|
[NCBI]
|
3.39935e-06
|
|
|
HLA-DPA1
|
[NCBI]
|
3.39935e-06
|
|
|
CX3CL1
|
[NCBI]
|
3.39935e-06
|
|
|
SNN
|
[NCBI]
|
3.39935e-06
|
|
|
GABRB3
|
[NCBI]
|
3.39935e-06
|
|
|
oncogene dj1
|
[NCBI]
|
3.39935e-06
|
|
|
pta deficiency
|
[NCBI]
|
3.39935e-06
|
|
|
PTPN6
|
[NCBI]
|
3.39935e-06
|
|
|
HIC1
|
[NCBI]
|
3.39935e-06
|
|
|
WNT3A
|
[NCBI]
|
3.39935e-06
|
|
|
TFAP2A
|
[NCBI]
|
3.39935e-06
|
|
|
PRDX5
|
[NCBI]
|
3.39935e-06
|
|
|
DYT1
|
[NCBI]
|
3.39935e-06
|
|
|
MEG3
|
[NCBI]
|
3.39935e-06
|
|
|
ZNF9
|
[NCBI]
|
3.39935e-06
|
|
|
LSA
|
[NCBI]
|
3.36743e-06
|
|
|
TFPI
|
[NCBI]
|
3.35674e-06
|
|
|
TIMP1
|
[NCBI]
|
3.33169e-06
|
|
|
CUTL1
|
[NCBI]
|
3.33169e-06
|
|
|
SOD1
|
[NCBI]
|
3.17847e-06
|
|
|
APP
|
[NCBI]
|
3.15617e-06
|
|
|
AHC
|
[NCBI]
|
3.14952e-06
|
|
|
TLR4
|
[NCBI]
|
3.05868e-06
|
|
|
AGER
|
[NCBI]
|
2.99532e-06
|
|
|
FTCD
|
[NCBI]
|
2.99531e-06
|
|
|
IDH1
|
[NCBI]
|
2.99531e-06
|
|
|
PMM2
|
[NCBI]
|
2.99531e-06
|
|
|
SKI
|
[NCBI]
|
2.99531e-06
|
|
|
PAPPA
|
[NCBI]
|
2.99531e-06
|
|
|
RPS3
|
[NCBI]
|
2.99531e-06
|
|
|
TBX3
|
[NCBI]
|
2.99531e-06
|
|
|
PZP
|
[NCBI]
|
2.99531e-06
|
|
|
TNFRSF10C
|
[NCBI]
|
2.99531e-06
|
|
|
INVS
|
[NCBI]
|
2.99531e-06
|
|
|
ASNS
|
[NCBI]
|
2.99531e-06
|
|
|
PAK3
|
[NCBI]
|
2.99531e-06
|
|
|
LRE1
|
[NCBI]
|
2.99531e-06
|
|
|
FOXE1
|
[NCBI]
|
2.99531e-06
|
|
|
PEG3
|
[NCBI]
|
2.99531e-06
|
|
|
PRKCZ
|
[NCBI]
|
2.99531e-06
|
|
|
SLPI
|
[NCBI]
|
2.90881e-06
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
2.90178e-06
|
|
|
DMPK
|
[NCBI]
|
2.90178e-06
|
|
|
LPO
|
[NCBI]
|
2.85832e-06
|
|
|
ASS
|
[NCBI]
|
2.75261e-06
|
|
|
IFNA1
|
[NCBI]
|
2.72058e-06
|
|
|
FGF10
|
[NCBI]
|
2.70383e-06
|
|
|
PJS
|
[NCBI]
|
2.6889e-06
|
|
|
ADA
|
[NCBI]
|
2.6609e-06
|
|
|
SLC11A2
|
[NCBI]
|
2.64807e-06
|
|
|
IL3
|
[NCBI]
|
2.64807e-06
|
|
|
CMPK1
|
[NCBI]
|
2.6376e-06
|
|
|
MEF2A
|
[NCBI]
|
2.6376e-06
|
|
|
SNX1
|
[NCBI]
|
2.6376e-06
|
|
|
RAB27A
|
[NCBI]
|
2.6376e-06
|
|
|
LIMK1
|
[NCBI]
|
2.6376e-06
|
|
|
SOAT1
|
[NCBI]
|
2.6376e-06
|
|
|
ITGAV
|
[NCBI]
|
2.6376e-06
|
|
|
SEMA3F
|
[NCBI]
|
2.6376e-06
|
|
|
RHOA
|
[NCBI]
|
2.6376e-06
|
|
|
GPHN
|
[NCBI]
|
2.6376e-06
|
|
|
SRA2
|
[NCBI]
|
2.6376e-06
|
|
|
MTHFR
|
[NCBI]
|
2.6376e-06
|
|
|
ANTXR1
|
[NCBI]
|
2.6376e-06
|
|
|
CEBPA
|
[NCBI]
|
2.6376e-06
|
|
|
MADHIP
|
[NCBI]
|
2.6376e-06
|
|
|
ETS2
|
[NCBI]
|
2.6376e-06
|
|
|
COFS1
|
[NCBI]
|
2.56943e-06
|
|
|
chromosome 5q deletion syndrome
|
[NCBI]
|
2.56943e-06
|
|
|
MVA
|
[NCBI]
|
2.56943e-06
|
|
|
ALMS
|
[NCBI]
|
2.56943e-06
|
|
|
UCP1
|
[NCBI]
|
2.48931e-06
|
|
|
TNFRSF1A
|
[NCBI]
|
2.44263e-06
|
|
|
GPI
|
[NCBI]
|
2.36622e-06
|
|
|
MVP
|
[NCBI]
|
2.34178e-06
|
|
|
ASL
|
[NCBI]
|
2.339e-06
|
|
|
PLP1
|
[NCBI]
|
2.339e-06
|
|
|
PFKL
|
[NCBI]
|
2.31956e-06
|
|
|
UBE1
|
[NCBI]
|
2.31956e-06
|
|
|
LEF1
|
[NCBI]
|
2.31956e-06
|
|
|
CDK7
|
[NCBI]
|
2.31956e-06
|
|
|
EPB41
|
[NCBI]
|
2.31956e-06
|
|
|
PER2
|
[NCBI]
|
2.31956e-06
|
|
|
DNMT3A
|
[NCBI]
|
2.31956e-06
|
|
|
POLD1
|
[NCBI]
|
2.31956e-06
|
|
|
HSF1
|
[NCBI]
|
2.31956e-06
|
|
|
EPOR
|
[NCBI]
|
2.30232e-06
|
|
|
SERPINA6
|
[NCBI]
|
2.30232e-06
|
|
|
CLU
|
[NCBI]
|
2.24224e-06
|
|
|
KIT
|
[NCBI]
|
2.17105e-06
|
|
|
SCP2
|
[NCBI]
|
2.17105e-06
|
|
|
MAP3K5
|
[NCBI]
|
2.09105e-06
|
|
|
STC1
|
[NCBI]
|
2.04719e-06
|
|
|
CDPX2
|
[NCBI]
|
2.04205e-06
|
|
|
UBE3A
|
[NCBI]
|
2.0359e-06
|
|
|
JARID2
|
[NCBI]
|
2.0359e-06
|
|
|
ENO1
|
[NCBI]
|
2.0359e-06
|
|
|
IRF7
|
[NCBI]
|
2.0359e-06
|
|
|
FTH1
|
[NCBI]
|
2.0359e-06
|
|
|
MAPK9
|
[NCBI]
|
2.0359e-06
|
|
|
TAZ
|
[NCBI]
|
2.0359e-06
|
|
|
TERF1
|
[NCBI]
|
2.0359e-06
|
|
|
PLAT
|
[NCBI]
|
2.0359e-06
|
|
|
PTTG1
|
[NCBI]
|
2.0359e-06
|
|
|
IKZF1
|
[NCBI]
|
2.0359e-06
|
|
|
PHB
|
[NCBI]
|
2.0359e-06
|
|
|
JMJD6
|
[NCBI]
|
2.0359e-06
|
|
|
BMP1
|
[NCBI]
|
2.0359e-06
|
|
|
BTRC
|
[NCBI]
|
2.0359e-06
|
|
|
RELA
|
[NCBI]
|
2.0359e-06
|
|
|
adipocyte-derived leucine aminopeptidase
|
[NCBI]
|
2.0359e-06
|
|
|
MYH11
|
[NCBI]
|
2.01212e-06
|
|
|
AHR
|
[NCBI]
|
2.00163e-06
|
|
|
AHO
|
[NCBI]
|
1.88115e-06
|
|
|
EDMD2
|
[NCBI]
|
1.87138e-06
|
|
|
mulibrey nanism
|
[NCBI]
|
1.87138e-06
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
1.87138e-06
|
|
|
myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|
[NCBI]
|
1.87138e-06
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
1.87138e-06
|
|
|
AEZ
|
[NCBI]
|
1.87138e-06
|
|
|
TNFSF11
|
[NCBI]
|
1.86695e-06
|
|
|
AKT1
|
[NCBI]
|
1.86177e-06
|
|
|
LHCGR
|
[NCBI]
|
1.86177e-06
|
|
|
FGF8
|
[NCBI]
|
1.85779e-06
|
|
|
BRCA1
|
[NCBI]
|
1.84955e-06
|
|
|
FMR1
|
[NCBI]
|
1.84087e-06
|
|
|
TF
|
[NCBI]
|
1.81718e-06
|
|
|
MYO5A
|
[NCBI]
|
1.78231e-06
|
|
|
PTGS1
|
[NCBI]
|
1.78231e-06
|
|
|
BMP7
|
[NCBI]
|
1.78231e-06
|
|
|
HSPCA
|
[NCBI]
|
1.78231e-06
|
|
|
CHRNA1
|
[NCBI]
|
1.78231e-06
|
|
|
MICA
|
[NCBI]
|
1.78231e-06
|
|
|
SMAD2
|
[NCBI]
|
1.78231e-06
|
|
|
RXRA
|
[NCBI]
|
1.78231e-06
|
|
|
IL1A
|
[NCBI]
|
1.78231e-06
|
|
|
PAK2
|
[NCBI]
|
1.78231e-06
|
|
|
DKC1
|
[NCBI]
|
1.78231e-06
|
|
|
EPHB2
|
[NCBI]
|
1.78231e-06
|
|
|
GJB3
|
[NCBI]
|
1.78231e-06
|
|
|
GLUD1
|
[NCBI]
|
1.78231e-06
|
|
|
CLDN11
|
[NCBI]
|
1.78231e-06
|
|
|
CD1D
|
[NCBI]
|
1.78231e-06
|
|
|
RASA1
|
[NCBI]
|
1.75827e-06
|
|
|
ITGB3
|
[NCBI]
|
1.71958e-06
|
|
|
NGFR
|
[NCBI]
|
1.71634e-06
|
|
|
CBX5
|
[NCBI]
|
1.68965e-06
|
|
|
PAX6
|
[NCBI]
|
1.67435e-06
|
|
|
ARNT
|
[NCBI]
|
1.67435e-06
|
|
|
costello syndrome
|
[NCBI]
|
1.65879e-06
|
|
|
MITF
|
[NCBI]
|
1.58051e-06
|
|
|
POLR2A
|
[NCBI]
|
1.55524e-06
|
|
|
MIF
|
[NCBI]
|
1.55524e-06
|
|
|
WIPF1
|
[NCBI]
|
1.55524e-06
|
|
|
TSIX
|
[NCBI]
|
1.55524e-06
|
|
|
DLL1
|
[NCBI]
|
1.55524e-06
|
|
|
OPA1
|
[NCBI]
|
1.55524e-06
|
|
|
ACTA1
|
[NCBI]
|
1.55524e-06
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
1.54585e-06
|
|
|
LBP
|
[NCBI]
|
1.49724e-06
|
|
|
ZFP36
|
[NCBI]
|
1.4331e-06
|
|
|
WT1
|
[NCBI]
|
1.43082e-06
|
|
|
NOTCH1
|
[NCBI]
|
1.41118e-06
|
|
|
FGFR1
|
[NCBI]
|
1.37748e-06
|
|
|
FOP
|
[NCBI]
|
1.36416e-06
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
1.36416e-06
|
|
|
PPARD
|
[NCBI]
|
1.35175e-06
|
|
|
ID2
|
[NCBI]
|
1.35175e-06
|
|
|
FUS
|
[NCBI]
|
1.35175e-06
|
|
|
GSK3B
|
[NCBI]
|
1.35175e-06
|
|
|
P4HB
|
[NCBI]
|
1.35175e-06
|
|
|
KRT20
|
[NCBI]
|
1.32686e-06
|
|
|
IGFALS
|
[NCBI]
|
1.32686e-06
|
|
|
HDAC1
|
[NCBI]
|
1.31215e-06
|
|
|
GACI
|
[NCBI]
|
1.3086e-06
|
|
|
HSAN3
|
[NCBI]
|
1.30814e-06
|
|
|
SJS1
|
[NCBI]
|
1.30814e-06
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
1.30814e-06
|
|
|
PTN
|
[NCBI]
|
1.27779e-06
|
|
|
phenylketonuria
|
[NCBI]
|
1.24432e-06
|
|
|
APOD
|
[NCBI]
|
1.22543e-06
|
|
|
DNTT
|
[NCBI]
|
1.22543e-06
|
|
|
FTL
|
[NCBI]
|
1.16935e-06
|
|
|
MAP2K1
|
[NCBI]
|
1.16935e-06
|
|
|
PTPN1
|
[NCBI]
|
1.16935e-06
|
|
|
MAP4
|
[NCBI]
|
1.16935e-06
|
|
|
PPID
|
[NCBI]
|
1.16935e-06
|
|
|
FOS
|
[NCBI]
|
1.16935e-06
|
|
|
ATP2A2
|
[NCBI]
|
1.16935e-06
|
|
|
MTND5
|
[NCBI]
|
1.16935e-06
|
|
|
TNFRSF10A
|
[NCBI]
|
1.16935e-06
|
|
|
ITGB4
|
[NCBI]
|
1.16935e-06
|
|
|
UNG
|
[NCBI]
|
1.16935e-06
|
|
|
BRAF
|
[NCBI]
|
1.16935e-06
|
|
|
TRIM27
|
[NCBI]
|
1.16935e-06
|
|
|
CEACAM1
|
[NCBI]
|
1.16363e-06
|
|
|
LCN2
|
[NCBI]
|
1.16363e-06
|
|
|
CASR
|
[NCBI]
|
1.12356e-06
|
|
|
DFFB
|
[NCBI]
|
1.11895e-06
|
|
|
CALCRL
|
[NCBI]
|
1.07152e-06
|
|
|
TNFSF10
|
[NCBI]
|
1.06805e-06
|
|
|
SHH
|
[NCBI]
|
1.03985e-06
|
|
|
PLK1
|
[NCBI]
|
1.03725e-06
|
|
|
LAM
|
[NCBI]
|
1.02698e-06
|
|
|
MTTL1
|
[NCBI]
|
1.01873e-06
|
|
|
TSHR
|
[NCBI]
|
1.01873e-06
|
|
|
CD36
|
[NCBI]
|
1.00802e-06
|
|
|
TYR
|
[NCBI]
|
1.00802e-06
|
|
|
BTC
|
[NCBI]
|
1.00802e-06
|
|
|
AICDA
|
[NCBI]
|
1.00593e-06
|
|
|
RPS19
|
[NCBI]
|
1.00593e-06
|
|
|
GSTP1
|
[NCBI]
|
1.00593e-06
|
|
|
MTND6
|
[NCBI]
|
1.00593e-06
|
|
|
KLF6
|
[NCBI]
|
1.00593e-06
|
|
|
DNM1L
|
[NCBI]
|
1.00593e-06
|
|
|
COL4A1
|
[NCBI]
|
1.00593e-06
|
|
|
EEF2
|
[NCBI]
|
1.00593e-06
|
|
|
GJA1
|
[NCBI]
|
9.46489e-07
|
|
|
LBR
|
[NCBI]
|
9.33235e-07
|
|
|
GCCR
|
[NCBI]
|
9.24506e-07
|
|
|
LPG
|
[NCBI]
|
8.6414e-07
|
|
|
lynch syndrome i
|
[NCBI]
|
8.6414e-07
|
|
|
aortic aneurysm, abdominal
|
[NCBI]
|
8.6414e-07
|
|
|
GABEB
|
[NCBI]
|
8.6414e-07
|
|
|
danon disease
|
[NCBI]
|
8.6414e-07
|
|
|
septooptic dysplasia
|
[NCBI]
|
8.6414e-07
|
|
|
HD
|
[NCBI]
|
8.62578e-07
|
|
|
CASP3
|
[NCBI]
|
8.59678e-07
|
|
|
TSG101
|
[NCBI]
|
8.59678e-07
|
|
|
PGP
|
[NCBI]
|
8.59678e-07
|
|
|
TYRP1
|
[NCBI]
|
8.59678e-07
|
|
|
ADK
|
[NCBI]
|
8.59678e-07
|
|
|
CRY2
|
[NCBI]
|
8.59678e-07
|
|
|
EBF
|
[NCBI]
|
8.59678e-07
|
|
|
KLF2
|
[NCBI]
|
8.59678e-07
|
|
|
HAS2
|
[NCBI]
|
8.59678e-07
|
|
|
PER1
|
[NCBI]
|
8.59678e-07
|
|
|
SKP2
|
[NCBI]
|
8.59678e-07
|
|
|
MMP2
|
[NCBI]
|
7.53137e-07
|
|
|
ND
|
[NCBI]
|
7.4785e-07
|
|
|
FGFR2
|
[NCBI]
|
7.29602e-07
|
|
|
IL2RG
|
[NCBI]
|
7.29031e-07
|
|
|
TMOD
|
[NCBI]
|
7.29031e-07
|
|
|
FSTL3
|
[NCBI]
|
7.29031e-07
|
|
|
SLC25A4
|
[NCBI]
|
7.29031e-07
|
|
|
ITGB1
|
[NCBI]
|
7.29031e-07
|
|
|
HBEGF
|
[NCBI]
|
7.29031e-07
|
|
|
ADRB2
|
[NCBI]
|
7.29031e-07
|
|
|
HSPA1A
|
[NCBI]
|
7.29031e-07
|
|
|
DDIT3
|
[NCBI]
|
7.29031e-07
|
|
|
HMGA2
|
[NCBI]
|
7.29031e-07
|
|
|
BCL2
|
[NCBI]
|
7.21819e-07
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
7.14244e-07
|
|
|
INS
|
[NCBI]
|
7.03003e-07
|
|
|
PTGS2
|
[NCBI]
|
6.79555e-07
|
|
|
COL2A1
|
[NCBI]
|
6.75555e-07
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
6.71286e-07
|
|
|
von willebrand disease
|
[NCBI]
|
6.55918e-07
|
|
|
MYO7A
|
[NCBI]
|
6.12631e-07
|
|
|
MYCN
|
[NCBI]
|
6.12631e-07
|
|
|
NUP98
|
[NCBI]
|
6.12631e-07
|
|
|
GSN
|
[NCBI]
|
6.12631e-07
|
|
|
ETS1
|
[NCBI]
|
6.12631e-07
|
|
|
HK1
|
[NCBI]
|
6.12631e-07
|
|
|
TIMP3
|
[NCBI]
|
6.12631e-07
|
|
|
COL17A1
|
[NCBI]
|
6.12631e-07
|
|
|
NOS2A
|
[NCBI]
|
6.12631e-07
|
|
|
HLA-A
|
[NCBI]
|
6.03103e-07
|
|
|
ESD
|
[NCBI]
|
5.36248e-07
|
|
|
HEMB
|
[NCBI]
|
5.35595e-07
|
|
|
usher syndrome, type i
|
[NCBI]
|
5.24065e-07
|
|
|
uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to
|
[NCBI]
|
5.24065e-07
|
|
|
glutaric acidemia i
|
[NCBI]
|
5.24065e-07
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
5.24065e-07
|
|
|
asplenia with cardiovascular anomalies
|
[NCBI]
|
5.24065e-07
|
|
|
PRKAR1A
|
[NCBI]
|
5.09291e-07
|
|
|
PIAS1
|
[NCBI]
|
5.09291e-07
|
|
|
HDAC4
|
[NCBI]
|
5.09291e-07
|
|
|
FANCA
|
[NCBI]
|
5.09291e-07
|
|
|
GPC3
|
[NCBI]
|
5.09291e-07
|
|
|
HSPB1
|
[NCBI]
|
5.09291e-07
|
|
|
IGKC
|
[NCBI]
|
5.09291e-07
|
|
|
FSHR
|
[NCBI]
|
4.73143e-07
|
|
|
PVR
|
[NCBI]
|
4.73143e-07
|
|
|
EGFR
|
[NCBI]
|
4.52396e-07
|
|
|
PDCD8
|
[NCBI]
|
4.41299e-07
|
|
|
CD59
|
[NCBI]
|
4.17964e-07
|
|
|
HGFAC
|
[NCBI]
|
4.17964e-07
|
|
|
GZMB
|
[NCBI]
|
4.17964e-07
|
|
|
PPARGC1A
|
[NCBI]
|
4.17964e-07
|
|
|
SHOX
|
[NCBI]
|
4.17964e-07
|
|
|
CDC42
|
[NCBI]
|
4.17964e-07
|
|
|
IGHG1
|
[NCBI]
|
4.17964e-07
|
|
|
PPIB
|
[NCBI]
|
4.17964e-07
|
|
|
FOXO3A
|
[NCBI]
|
4.17964e-07
|
|
|
TNFRSF6B
|
[NCBI]
|
4.17964e-07
|
|
|
ATF4
|
[NCBI]
|
4.17964e-07
|
|
|
MAP1B
|
[NCBI]
|
4.17518e-07
|
|
|
TFRC
|
[NCBI]
|
3.64718e-07
|
|
|
DCT
|
[NCBI]
|
3.64718e-07
|
|
|
ATF3
|
[NCBI]
|
3.60993e-07
|
|
|
STK11
|
[NCBI]
|
3.37727e-07
|
|
|
CDKN1B
|
[NCBI]
|
3.37727e-07
|
|
|
IRS2
|
[NCBI]
|
3.37727e-07
|
|
|
PTHR1
|
[NCBI]
|
3.37727e-07
|
|
|
RLBP1
|
[NCBI]
|
3.1486e-07
|
|
|
PARG
|
[NCBI]
|
3.1486e-07
|
|
|
APOE
|
[NCBI]
|
3.07114e-07
|
|
|
NRG1
|
[NCBI]
|
2.94878e-07
|
|
|
MAP2
|
[NCBI]
|
2.69151e-07
|
|
|
IRS1
|
[NCBI]
|
2.68065e-07
|
|
|
MLL
|
[NCBI]
|
2.68065e-07
|
|
|
A2M
|
[NCBI]
|
2.67756e-07
|
|
|
coproporphyria
|
[NCBI]
|
2.67756e-07
|
|
|
CYBB
|
[NCBI]
|
2.67756e-07
|
|
|
DSG1
|
[NCBI]
|
2.67756e-07
|
|
|
IP
|
[NCBI]
|
2.51322e-07
|
|
|
UMOD
|
[NCBI]
|
2.07319e-07
|
|
|
NCOA3
|
[NCBI]
|
2.07319e-07
|
|
|
ALDH1A2
|
[NCBI]
|
2.07319e-07
|
|
|
FPRL1
|
[NCBI]
|
2.07319e-07
|
|
|
H6PD
|
[NCBI]
|
2.07319e-07
|
|
|
ICAM1
|
[NCBI]
|
2.07319e-07
|
|
|
UBTF
|
[NCBI]
|
1.87588e-07
|
|
|
RET
|
[NCBI]
|
1.87588e-07
|
|
|
SLC6A6
|
[NCBI]
|
1.84195e-07
|
|
|
PI
|
[NCBI]
|
1.70901e-07
|
|
|
EDMD
|
[NCBI]
|
1.623e-07
|
|
|
ED1
|
[NCBI]
|
1.623e-07
|
|
|
IKBKB
|
[NCBI]
|
1.55758e-07
|
|
|
HDGF
|
[NCBI]
|
1.55758e-07
|
|
|
STAT5B
|
[NCBI]
|
1.55758e-07
|
|
|
HMI
|
[NCBI]
|
1.55758e-07
|
|
|
REST
|
[NCBI]
|
1.47408e-07
|
|
|
DAZ
|
[NCBI]
|
1.47408e-07
|
|
|
GCK
|
[NCBI]
|
1.47408e-07
|
|
|
DCC
|
[NCBI]
|
1.47408e-07
|
|
|
WT1
|
[NCBI]
|
1.47408e-07
|
|
|
HMGB1
|
[NCBI]
|
1.47408e-07
|
|
|
RELN
|
[NCBI]
|
1.47408e-07
|
|
|
CMD1A
|
[NCBI]
|
1.35531e-07
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
1.35531e-07
|
|
|
TYMS
|
[NCBI]
|
1.19343e-07
|
|
|
ARF6
|
[NCBI]
|
1.1426e-07
|
|
|
HBG1
|
[NCBI]
|
1.1248e-07
|
|
|
TNFRSF1B
|
[NCBI]
|
1.1248e-07
|
|
|
TNFSF13B
|
[NCBI]
|
1.1248e-07
|
|
|
OA1
|
[NCBI]
|
1.1248e-07
|
|
|
aHUS
|
[NCBI]
|
1.12442e-07
|
|
|
SEDC
|
[NCBI]
|
1.12442e-07
|
|
|
HAE
|
[NCBI]
|
1.12442e-07
|
|
|
UMS
|
[NCBI]
|
1.12442e-07
|
|
|
EFE
|
[NCBI]
|
1.12442e-07
|
|
|
ARF1
|
[NCBI]
|
8.492e-08
|
|
|
CHGA
|
[NCBI]
|
7.69512e-08
|
|
|
AGTR1
|
[NCBI]
|
7.69512e-08
|
|
|
CTSC
|
[NCBI]
|
7.69512e-08
|
|
|
apc gene
|
[NCBI]
|
7.68239e-08
|
|
|
AQP1
|
[NCBI]
|
7.68239e-08
|
|
|
SOCS3
|
[NCBI]
|
7.42918e-08
|
|
|
MAPK1
|
[NCBI]
|
6.46593e-08
|
|
|
GH1
|
[NCBI]
|
5.957e-08
|
|
|
SOCS1
|
[NCBI]
|
4.86868e-08
|
|
|
TPI1
|
[NCBI]
|
4.86868e-08
|
|
|
GALT
|
[NCBI]
|
4.86868e-08
|
|
|
BACE1
|
[NCBI]
|
4.86868e-08
|
|
|
CXCL12
|
[NCBI]
|
4.86868e-08
|
|
|
CHNG2
|
[NCBI]
|
4.01013e-08
|
|
|
MELAS
|
[NCBI]
|
4.01013e-08
|
|
|
MST1
|
[NCBI]
|
3.84043e-08
|
|
|
SPARC
|
[NCBI]
|
3.79232e-08
|
|
|
DNMT1
|
[NCBI]
|
3.7755e-08
|
|
|
RUNX2
|
[NCBI]
|
2.72463e-08
|
|
|
LIFR
|
[NCBI]
|
2.72463e-08
|
|
|
SNRPN
|
[NCBI]
|
2.72463e-08
|
|
|
IL13
|
[NCBI]
|
2.72463e-08
|
|
|
GDXY
|
[NCBI]
|
2.72463e-08
|
|
|
PTHLH
|
[NCBI]
|
2.6519e-08
|
|
|
AN2
|
[NCBI]
|
2.62072e-08
|
|
|
thrombocythemia, essential
|
[NCBI]
|
2.28119e-08
|
|
|
MSS
|
[NCBI]
|
2.28119e-08
|
|
|
DSTN
|
[NCBI]
|
2.16323e-08
|
|
|
BGN
|
[NCBI]
|
2.16323e-08
|
|
|
LIPC
|
[NCBI]
|
1.89621e-08
|
|
|
APOB
|
[NCBI]
|
1.59414e-08
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
1.22284e-08
|
|
|
PAFAH1B1
|
[NCBI]
|
1.22284e-08
|
|
|
VLDLR
|
[NCBI]
|
1.22284e-08
|
|
|
TPT1
|
[NCBI]
|
9.47924e-09
|
|
|
IFNG
|
[NCBI]
|
9.47924e-09
|
|
|
KAL1
|
[NCBI]
|
9.47924e-09
|
|
|
SMA1
|
[NCBI]
|
7.48015e-09
|
|
|
FXN
|
[NCBI]
|
3.26583e-09
|
|
|
TSC2
|
[NCBI]
|
3.26583e-09
|
|
|
ANG
|
[NCBI]
|
3.26583e-09
|
|
|
ATF2
|
[NCBI]
|
3.26583e-09
|
|
|
CHS
|
[NCBI]
|
2.24645e-09
|
|
|
DES
|
[NCBI]
|
2.18824e-09
|
|
|
TACR1
|
[NCBI]
|
2.18824e-09
|
|
|
STAT3
|
[NCBI]
|
1.42107e-09
|
|
|
sickle cell anemia
|
[NCBI]
|
7.47021e-10
|
|
|
PRKCM
|
[NCBI]
|
4.7316e-10
|
|
|
TLR9
|
[NCBI]
|
4.7316e-10
|
|
|
KSS
|
[NCBI]
|
3.11942e-10
|
|
|
FGF2
|
[NCBI]
|
8.87745e-11
|
|
|
STAT6
|
[NCBI]
|
4.43708e-11
|
|
|
NF2
|
[NCBI]
|
2.21813e-11
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
2.21813e-11
|
|
|
CXCR4
|
[NCBI]
|
2.21813e-11
|
|
|
BAX
|
[NCBI]
|
2.21813e-11
|
|
|
INHBA
|
[NCBI]
|
2.21813e-11
|
|
|
FABP3
|
[NCBI]
|
2.21813e-11
|
|
|
MTND1
|
[NCBI]
|
2.21813e-11
|
|