|
OMIM |
Link |
Information gain |
01 |
|
AOS
|
[NCBI]
|
0.00818887
|
|
|
FRNS
|
[NCBI]
|
0.00203817
|
|
|
campomelia, cumming type
|
[NCBI]
|
0.00182132
|
|
|
mesomelia-synostoses syndrome
|
[NCBI]
|
0.00144724
|
|
|
SHFM3
|
[NCBI]
|
0.00142372
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.00106854
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.00104681
|
|
|
nievergelt syndrome
|
[NCBI]
|
0.00101446
|
|
|
EEC1
|
[NCBI]
|
0.000993313
|
|
|
SHFM5
|
[NCBI]
|
0.000922877
|
|
|
acromelic frontonasal dysostosis
|
[NCBI]
|
0.000853061
|
|
|
SHH
|
[NCBI]
|
0.000792018
|
|
|
acropectoral syndrome
|
[NCBI]
|
0.000722776
|
|
|
geleophysic dysplasia
|
[NCBI]
|
0.000673032
|
|
|
DA5
|
[NCBI]
|
0.000673032
|
|
|
CDLS1
|
[NCBI]
|
0.000645931
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
0.000616723
|
|
|
POADS
|
[NCBI]
|
0.000586993
|
|
|
GDF5
|
[NCBI]
|
0.000521642
|
|
|
acromicric dysplasia
|
[NCBI]
|
0.000506401
|
|
|
trichoscyphodysplasia
|
[NCBI]
|
0.000506401
|
|
|
ODDD
|
[NCBI]
|
0.000454015
|
|
|
DA4
|
[NCBI]
|
0.000425718
|
|
|
spondylometaphyseal dysplasia, corner fracture type
|
[NCBI]
|
0.000425718
|
|
|
triphalangeal thumbs with brachyectrodactyly
|
[NCBI]
|
0.000425718
|
|
|
mesomelic dysplasia, kantaputra type
|
[NCBI]
|
0.000425718
|
|
|
HOS
|
[NCBI]
|
0.000380035
|
|
|
NLS
|
[NCBI]
|
0.00037633
|
|
|
omodysplasia
|
[NCBI]
|
0.000373879
|
|
|
chondrodysplasia, grebe type
|
[NCBI]
|
0.000363556
|
|
|
TP73L
|
[NCBI]
|
0.000340874
|
|
|
opsismodysplasia
|
[NCBI]
|
0.000335737
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.000335737
|
|
|
adult syndrome
|
[NCBI]
|
0.000335646
|
|
|
ROR2
|
[NCBI]
|
0.000312987
|
|
|
EEC3
|
[NCBI]
|
0.000309292
|
|
|
femur, unilateral bifid, with monodactylous ectrodactyly
|
[NCBI]
|
0.000305665
|
|
|
ATD1
|
[NCBI]
|
0.000286209
|
|
|
sclerotylosis
|
[NCBI]
|
0.000280923
|
|
|
SHFM2
|
[NCBI]
|
0.000280923
|
|
|
microphthalmia with limb anomalies
|
[NCBI]
|
0.000280923
|
|
|
peters-plus syndrome
|
[NCBI]
|
0.000280429
|
|
|
SHFM1
|
[NCBI]
|
0.000271878
|
|
|
cranioectodermal dysplasia
|
[NCBI]
|
0.000259971
|
|
|
popliteal pterygium syndrome, lethal type
|
[NCBI]
|
0.000259971
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000258467
|
|
|
omodysplasia, generalized form
|
[NCBI]
|
0.000241852
|
|
|
spondyloepimetaphyseal dysplasia, sponastrime type
|
[NCBI]
|
0.000241852
|
|
|
acrodysostosis
|
[NCBI]
|
0.000241852
|
|
|
LMS
|
[NCBI]
|
0.000239915
|
|
|
RBS
|
[NCBI]
|
0.000237334
|
|
|
acrorenal-mandibular syndrome
|
[NCBI]
|
0.000230764
|
|
|
camptomelic syndrome, long-limb type
|
[NCBI]
|
0.000230764
|
|
|
OPD2
|
[NCBI]
|
0.000230663
|
|
|
gordon syndrome
|
[NCBI]
|
0.000225933
|
|
|
ear, patella, short stature syndrome
|
[NCBI]
|
0.000225933
|
|
|
tibia, hypoplasia of, with polydactyly
|
[NCBI]
|
0.000225933
|
|
|
PHS
|
[NCBI]
|
0.000224931
|
|
|
GCPS
|
[NCBI]
|
0.000223045
|
|
|
BDA2
|
[NCBI]
|
0.000217942
|
|
|
SLOS
|
[NCBI]
|
0.000213758
|
|
|
kyphomelic dysplasia
|
[NCBI]
|
0.00021177
|
|
|
SALL1
|
[NCBI]
|
0.000202586
|
|
|
SHFLD1
|
[NCBI]
|
0.000199043
|
|
|
microcephalic osteodysplastic primordial dwarfism, type ii
|
[NCBI]
|
0.000199043
|
|
|
limb deficiencies, distal, with micrognathia
|
[NCBI]
|
0.000190084
|
|
|
TBX5
|
[NCBI]
|
0.00018911
|
|
|
vater association
|
[NCBI]
|
0.000181104
|
|
|
AMCN
|
[NCBI]
|
0.000176993
|
|
|
FMN
|
[NCBI]
|
0.000175286
|
|
|
BMPR1B
|
[NCBI]
|
0.000175286
|
|
|
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
[NCBI]
|
0.000167808
|
|
|
SYM1
|
[NCBI]
|
0.000167808
|
|
|
ACG1A
|
[NCBI]
|
0.00016734
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.00016734
|
|
|
COH1
|
[NCBI]
|
0.000166481
|
|
|
campomelic dysplasia
|
[NCBI]
|
0.000166481
|
|
|
spondylometaepiphyseal dysplasia, short limb-hand type
|
[NCBI]
|
0.000159175
|
|
|
genitopalatocardiac syndrome
|
[NCBI]
|
0.000159175
|
|
|
BDA6
|
[NCBI]
|
0.000159175
|
|
|
SRS
|
[NCBI]
|
0.000138651
|
|
|
aprosencephaly syndrome
|
[NCBI]
|
0.000135673
|
|
|
MADA
|
[NCBI]
|
0.000135544
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
0.000135374
|
|
|
SALL4
|
[NCBI]
|
0.000132082
|
|
|
aglossia-adactylia
|
[NCBI]
|
0.000128358
|
|
|
syndactyly, type iii
|
[NCBI]
|
0.000128358
|
|
|
valproate embryopathy, susceptibility to
|
[NCBI]
|
0.000122426
|
|
|
pseudodiastrophic dysplasia
|
[NCBI]
|
0.000122426
|
|
|
JAG2
|
[NCBI]
|
0.000120098
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.000116504
|
|
|
acromesomelic dysplasia, hunter-thompson type
|
[NCBI]
|
0.000113124
|
|
|
BDA1
|
[NCBI]
|
0.000109334
|
|
|
FGF8
|
[NCBI]
|
0.000108131
|
|
|
CMTC
|
[NCBI]
|
0.000107415
|
|
|
AMDM
|
[NCBI]
|
0.000105951
|
|
|
EN1
|
[NCBI]
|
0.000105647
|
|
|
PMX1
|
[NCBI]
|
0.000105647
|
|
|
NSDHL
|
[NCBI]
|
0.000101143
|
|
|
costello syndrome
|
[NCBI]
|
9.9739e-05
|
|
|
HFM
|
[NCBI]
|
9.95708e-05
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
9.75606e-05
|
|
|
BDC
|
[NCBI]
|
9.51995e-05
|
|
|
thoracomelic dysplasia
|
[NCBI]
|
9.50102e-05
|
|
|
mesomelic limb shortening and bowing
|
[NCBI]
|
9.50102e-05
|
|
|
diaphragmatic defects, limb deficiencies, and ossification defects of skull
|
[NCBI]
|
9.50102e-05
|
|
|
chondrodysplasia, acromesomelic, with genital anomalies
|
[NCBI]
|
9.50102e-05
|
|
|
craniosynostosis with ocular abnormalities and hallucal defects
|
[NCBI]
|
9.50102e-05
|
|
|
cortical blindness, retardation, and postaxial polydactyly
|
[NCBI]
|
9.50102e-05
|
|
|
cervical ribs, sprengel anomaly, anal atresia, and urethral obstruction
|
[NCBI]
|
9.50102e-05
|
|
|
microcephaly, facial abnormalities, micromelia, and mental retardation
|
[NCBI]
|
9.50102e-05
|
|
|
cardioskeletal syndrome, kuwaiti type
|
[NCBI]
|
9.50102e-05
|
|
|
rudiger syndrome
|
[NCBI]
|
9.50102e-05
|
|
|
ventricular extrasystoles with syncope, perodactyly, and robin sequence
|
[NCBI]
|
9.50102e-05
|
|
|
acrocephalopolysyndactyly type iii
|
[NCBI]
|
9.50102e-05
|
|
|
acrocraniofacial dysostosis
|
[NCBI]
|
9.50102e-05
|
|
|
growth retardation, small and puffy hands and feet, and eczema
|
[NCBI]
|
9.50102e-05
|
|
|
laryngeal atresia, encephalocele, and limb deformities
|
[NCBI]
|
9.50102e-05
|
|
|
SPD1
|
[NCBI]
|
9.30051e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
9.30051e-05
|
|
|
CHUK
|
[NCBI]
|
9.17437e-05
|
|
|
coffin-siris syndrome
|
[NCBI]
|
9.15679e-05
|
|
|
DMC
|
[NCBI]
|
9.09557e-05
|
|
|
LMBR1
|
[NCBI]
|
8.94001e-05
|
|
|
DRRS
|
[NCBI]
|
8.90338e-05
|
|
|
HOXA13
|
[NCBI]
|
8.73066e-05
|
|
|
IHH
|
[NCBI]
|
8.57878e-05
|
|
|
UMS
|
[NCBI]
|
8.55159e-05
|
|
|
RHS
|
[NCBI]
|
8.38974e-05
|
|
|
HOXD13
|
[NCBI]
|
7.92721e-05
|
|
|
PPS
|
[NCBI]
|
7.81661e-05
|
|
|
NKX2E
|
[NCBI]
|
7.4603e-05
|
|
|
b-cell immunodeficiency, distal limb anomalies, and urogenital malformations
|
[NCBI]
|
7.25837e-05
|
|
|
renal dysplasia-limb defects syndrome
|
[NCBI]
|
7.25837e-05
|
|
|
acrofacial dysostosis, catania type
|
[NCBI]
|
7.25837e-05
|
|
|
pelvic hypoplasia with lower-limb arthrogryposis
|
[NCBI]
|
7.25837e-05
|
|
|
arthrogryposis-like hand anomaly and sensorineural deafness
|
[NCBI]
|
7.25837e-05
|
|
|
deafness, autosomal recessive
|
[NCBI]
|
7.25837e-05
|
|
|
spondylometaphyseal dysplasia, east african type
|
[NCBI]
|
7.25837e-05
|
|
|
pterygium syndrome, multiple, autosomal dominant
|
[NCBI]
|
7.25837e-05
|
|
|
ZWINT
|
[NCBI]
|
6.94983e-05
|
|
|
HOXD1
|
[NCBI]
|
6.94983e-05
|
|
|
ZW10
|
[NCBI]
|
6.94983e-05
|
|
|
GDF7
|
[NCBI]
|
6.94983e-05
|
|
|
MBS
|
[NCBI]
|
6.90132e-05
|
|
|
DA2A
|
[NCBI]
|
6.73287e-05
|
|
|
FGFR2
|
[NCBI]
|
6.6894e-05
|
|
|
TBS
|
[NCBI]
|
6.5567e-05
|
|
|
hydrocephalus with cerebellar agenesis
|
[NCBI]
|
6.41476e-05
|
|
|
preaxial deficiency, postaxial polydactyly, and hypospadias
|
[NCBI]
|
6.41476e-05
|
|
|
fibular hypoplasia and complex brachydactyly
|
[NCBI]
|
6.41476e-05
|
|
|
rhizomelic syndrome
|
[NCBI]
|
6.41476e-05
|
|
|
acrocephalopolydactylous dysplasia
|
[NCBI]
|
6.41476e-05
|
|
|
metaphyseal anadysplasia
|
[NCBI]
|
6.41476e-05
|
|
|
limb defects, distal transverse, with mental retardation and spasticity
|
[NCBI]
|
6.41476e-05
|
|
|
rapadilino syndrome
|
[NCBI]
|
6.41476e-05
|
|
|
camera-marugo-cohen syndrome
|
[NCBI]
|
6.41476e-05
|
|
|
ACFD
|
[NCBI]
|
6.41476e-05
|
|
|
fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
|
[NCBI]
|
6.41476e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
6.20444e-05
|
|
|
GJA1
|
[NCBI]
|
6.06028e-05
|
|
|
oroacral syndrome, verloes-koulischer type
|
[NCBI]
|
5.86855e-05
|
|
|
coloboma of macula with type b brachydactyly
|
[NCBI]
|
5.86855e-05
|
|
|
TS
|
[NCBI]
|
5.86855e-05
|
|
|
weill-marchesani syndrome, autosomal dominant
|
[NCBI]
|
5.86855e-05
|
|
|
metachondromatosis
|
[NCBI]
|
5.86855e-05
|
|
|
MADB
|
[NCBI]
|
5.86855e-05
|
|
|
LWD
|
[NCBI]
|
5.80781e-05
|
|
|
SLC35D1
|
[NCBI]
|
5.57267e-05
|
|
|
PRRX2
|
[NCBI]
|
5.57267e-05
|
|
|
splenogonadal fusion with limb defects and micrognathia
|
[NCBI]
|
5.46356e-05
|
|
|
cerebellar vermis aplasia with associated features suggesting smith-lemli-opitz syndrome and meckel syndrome
|
[NCBI]
|
5.46356e-05
|
|
|
SPS
|
[NCBI]
|
5.14177e-05
|
|
|
SMC
|
[NCBI]
|
5.14177e-05
|
|
|
weyers acrofacial dysostosis
|
[NCBI]
|
5.14177e-05
|
|
|
SHFM4
|
[NCBI]
|
5.14177e-05
|
|
|
TRPS3
|
[NCBI]
|
5.14177e-05
|
|
|
GDF6
|
[NCBI]
|
5.05343e-05
|
|
|
SOX14
|
[NCBI]
|
5.05343e-05
|
|
|
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
|
[NCBI]
|
4.87494e-05
|
|
|
cerebrofrontofacial syndrome
|
[NCBI]
|
4.87494e-05
|
|
|
carpenter syndrome
|
[NCBI]
|
4.87494e-05
|
|
|
acrofacial dysostosis syndrome of rodriguez
|
[NCBI]
|
4.87494e-05
|
|
|
schneckenbecken dysplasia
|
[NCBI]
|
4.87494e-05
|
|
|
CLS
|
[NCBI]
|
4.8198e-05
|
|
|
INCENP
|
[NCBI]
|
4.71656e-05
|
|
|
SHOX2
|
[NCBI]
|
4.71656e-05
|
|
|
PITX1
|
[NCBI]
|
4.71656e-05
|
|
|
FBXW4
|
[NCBI]
|
4.71656e-05
|
|
|
SLC12A2
|
[NCBI]
|
4.71656e-05
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
4.64719e-05
|
|
|
gastroschisis
|
[NCBI]
|
4.64719e-05
|
|
|
rokitansky-kuster-hauser syndrome
|
[NCBI]
|
4.64719e-05
|
|
|
lujan-fryns syndrome
|
[NCBI]
|
4.64719e-05
|
|
|
chondrodysplasia punctata, tibia-metacarpal type
|
[NCBI]
|
4.64719e-05
|
|
|
NPS
|
[NCBI]
|
4.64163e-05
|
|
|
FGFR1
|
[NCBI]
|
4.54049e-05
|
|
|
CDAN1
|
[NCBI]
|
4.4663e-05
|
|
|
HOXD3
|
[NCBI]
|
4.4663e-05
|
|
|
MODY2
|
[NCBI]
|
4.44864e-05
|
|
|
whistling face syndrome, recessive form
|
[NCBI]
|
4.44864e-05
|
|
|
BDB1
|
[NCBI]
|
4.27276e-05
|
|
|
trismus-pseudocamptodactyly syndrome
|
[NCBI]
|
4.27276e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
4.27276e-05
|
|
|
EN2
|
[NCBI]
|
4.26705e-05
|
|
|
TD1
|
[NCBI]
|
4.24278e-05
|
|
|
DA1
|
[NCBI]
|
4.115e-05
|
|
|
ankyloblepharon-ectodermal defects-cleft lip/palate
|
[NCBI]
|
4.115e-05
|
|
|
omphalocele
|
[NCBI]
|
4.115e-05
|
|
|
EVC2
|
[NCBI]
|
4.10151e-05
|
|
|
PPD2
|
[NCBI]
|
3.97204e-05
|
|
|
FFS
|
[NCBI]
|
3.97204e-05
|
|
|
frank-ter haar syndrome
|
[NCBI]
|
3.95992e-05
|
|
|
PAPSS2
|
[NCBI]
|
3.95992e-05
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
3.86959e-05
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
3.84141e-05
|
|
|
acheiropody
|
[NCBI]
|
3.84141e-05
|
|
|
RNS
|
[NCBI]
|
3.84141e-05
|
|
|
LADD
|
[NCBI]
|
3.84141e-05
|
|
|
GINGF
|
[NCBI]
|
3.84141e-05
|
|
|
SYNS1
|
[NCBI]
|
3.84141e-05
|
|
|
CACNA1C
|
[NCBI]
|
3.83625e-05
|
|
|
TRPS1
|
[NCBI]
|
3.83625e-05
|
|
|
FGF10
|
[NCBI]
|
3.83625e-05
|
|
|
TBX3
|
[NCBI]
|
3.83625e-05
|
|
|
PAX9
|
[NCBI]
|
3.72648e-05
|
|
|
DA2B
|
[NCBI]
|
3.72121e-05
|
|
|
PTEN
|
[NCBI]
|
3.67984e-05
|
|
|
RAI1
|
[NCBI]
|
3.53823e-05
|
|
|
proteus syndrome
|
[NCBI]
|
3.49682e-05
|
|
|
LMX1B
|
[NCBI]
|
3.45621e-05
|
|
|
papillorenal syndrome
|
[NCBI]
|
3.31884e-05
|
|
|
anemia, dyserythropoietic congenital, type i
|
[NCBI]
|
3.31884e-05
|
|
|
SLC26A2
|
[NCBI]
|
3.31042e-05
|
|
|
EBP
|
[NCBI]
|
3.24501e-05
|
|
|
MCDS
|
[NCBI]
|
3.23335e-05
|
|
|
IRF6
|
[NCBI]
|
3.18376e-05
|
|
|
MSX1
|
[NCBI]
|
3.18376e-05
|
|
|
CD
|
[NCBI]
|
3.13086e-05
|
|
|
PHOX2B
|
[NCBI]
|
3.07182e-05
|
|
|
ORW2
|
[NCBI]
|
3.00353e-05
|
|
|
DHCR7
|
[NCBI]
|
2.97157e-05
|
|
|
NOG
|
[NCBI]
|
2.97157e-05
|
|
|
TRPS1
|
[NCBI]
|
2.93444e-05
|
|
|
PAX2
|
[NCBI]
|
2.88084e-05
|
|
|
NPHS1
|
[NCBI]
|
2.86855e-05
|
|
|
UCMD
|
[NCBI]
|
2.86855e-05
|
|
|
HSS
|
[NCBI]
|
2.86855e-05
|
|
|
GLI3
|
[NCBI]
|
2.83852e-05
|
|
|
ACVRL1
|
[NCBI]
|
2.798e-05
|
|
|
PHA
|
[NCBI]
|
2.74536e-05
|
|
|
ACLS
|
[NCBI]
|
2.74536e-05
|
|
|
diastrophic dysplasia
|
[NCBI]
|
2.74536e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
2.68761e-05
|
|
|
COL10A1
|
[NCBI]
|
2.68589e-05
|
|
|
OFD1
|
[NCBI]
|
2.63217e-05
|
|
|
RIEG1
|
[NCBI]
|
2.63217e-05
|
|
|
BMP4
|
[NCBI]
|
2.55453e-05
|
|
|
OKS
|
[NCBI]
|
2.52759e-05
|
|
|
CFNS
|
[NCBI]
|
2.52759e-05
|
|
|
ABS
|
[NCBI]
|
2.52759e-05
|
|
|
MKKS
|
[NCBI]
|
2.47816e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
2.47816e-05
|
|
|
CTNNB1
|
[NCBI]
|
2.41262e-05
|
|
|
SHOX
|
[NCBI]
|
2.41262e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
2.38443e-05
|
|
|
PKS
|
[NCBI]
|
2.38443e-05
|
|
|
HCH
|
[NCBI]
|
2.29684e-05
|
|
|
COL7A1
|
[NCBI]
|
2.2229e-05
|
|
|
RCDP1
|
[NCBI]
|
2.21472e-05
|
|
|
CDPX2
|
[NCBI]
|
2.21472e-05
|
|
|
apert syndrome
|
[NCBI]
|
2.21472e-05
|
|
|
PAX3
|
[NCBI]
|
1.93215e-05
|
|
|
SCS
|
[NCBI]
|
1.93038e-05
|
|
|
JPS
|
[NCBI]
|
1.67334e-05
|
|
|
MTTL1
|
[NCBI]
|
1.66646e-05
|
|
|
GNAS
|
[NCBI]
|
1.6551e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
1.63282e-05
|
|
|
RTS
|
[NCBI]
|
1.62308e-05
|
|
|
sotos syndrome
|
[NCBI]
|
1.62308e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
1.52873e-05
|
|
|
MKS1
|
[NCBI]
|
1.52873e-05
|
|
|
LMNA
|
[NCBI]
|
1.51983e-05
|
|
|
WS1
|
[NCBI]
|
1.50633e-05
|
|
|
FBN1
|
[NCBI]
|
1.39527e-05
|
|
|
TCOF
|
[NCBI]
|
1.38075e-05
|
|
|
AMC
|
[NCBI]
|
1.34196e-05
|
|
|
PTH
|
[NCBI]
|
1.30644e-05
|
|
|
SDS
|
[NCBI]
|
9.92077e-06
|
|
|
SMS
|
[NCBI]
|
8.12768e-06
|
|
|
ZS
|
[NCBI]
|
6.75464e-06
|
|
|
ACH
|
[NCBI]
|
6.66577e-06
|
|
|
BBS
|
[NCBI]
|
6.0739e-06
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
5.51819e-06
|
|
|
AFP
|
[NCBI]
|
3.8972e-06
|
|
|
BCNS
|
[NCBI]
|
3.35052e-06
|
|
|
FA
|
[NCBI]
|
2.41781e-06
|
|
|
CPI
|
[NCBI]
|
2.0421e-06
|
|
|
MFS
|
[NCBI]
|
7.96312e-07
|
|
|
HGF
|
[NCBI]
|
6.66706e-07
|
|
|
polycystic kidneys
|
[NCBI]
|
7.0653e-08
|
|