|
OMIM |
Link |
Information gain |
01 |
|
IS1
|
[NCBI]
|
0.0203953
|
|
|
spondylometaphyseal dysplasia, corner fracture type
|
[NCBI]
|
0.00278544
|
|
|
SCDO1
|
[NCBI]
|
0.00205983
|
|
|
AIC
|
[NCBI]
|
0.00191663
|
|
|
spondyloepimetaphyseal dysplasia, sponastrime type
|
[NCBI]
|
0.00186312
|
|
|
GO
|
[NCBI]
|
0.00172726
|
|
|
spondyloenchondrodysplasia
|
[NCBI]
|
0.00172726
|
|
|
spondylometaphyseal dysplasia, kozlowski type
|
[NCBI]
|
0.00143002
|
|
|
costovertebral segmentation anomalies
|
[NCBI]
|
0.00123999
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.00111067
|
|
|
HFM
|
[NCBI]
|
0.00106942
|
|
|
klippel-feil syndrome, autosomal dominant
|
[NCBI]
|
0.00101241
|
|
|
acrodysostosis
|
[NCBI]
|
0.000933263
|
|
|
arthrogryposis-like disorder
|
[NCBI]
|
0.000926331
|
|
|
bone size quantitative trait locus 3
|
[NCBI]
|
0.000926331
|
|
|
vertebral ossification, defect in, with nephrogenic rests
|
[NCBI]
|
0.000926331
|
|
|
SPOAN
|
[NCBI]
|
0.000926331
|
|
|
SEMDIT
|
[NCBI]
|
0.000926331
|
|
|
DBQD
|
[NCBI]
|
0.00076095
|
|
|
spondylocarpotarsal synostosis syndrome
|
[NCBI]
|
0.000634493
|
|
|
acropectorovertebral dysplasia, f-form of
|
[NCBI]
|
0.00061896
|
|
|
otoonychoperoneal syndrome
|
[NCBI]
|
0.00061896
|
|
|
scheuermann disease
|
[NCBI]
|
0.00061896
|
|
|
BMND2
|
[NCBI]
|
0.00061896
|
|
|
three m syndrome
|
[NCBI]
|
0.000603335
|
|
|
OPLL
|
[NCBI]
|
0.000578253
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
0.000557176
|
|
|
microcephalic osteodysplastic primordial dwarfism, type iii
|
[NCBI]
|
0.000505201
|
|
|
bone size quantitative trait locus 1
|
[NCBI]
|
0.000505201
|
|
|
spondylometaphyseal dysplasia, sedaghatian type
|
[NCBI]
|
0.000505201
|
|
|
spondyloepiphyseal dysplasia tarda, autosomal dominant
|
[NCBI]
|
0.000505201
|
|
|
proteus syndrome
|
[NCBI]
|
0.000441493
|
|
|
HCH
|
[NCBI]
|
0.000436298
|
|
|
hypertrichotic osteochondrodysplasia
|
[NCBI]
|
0.000432597
|
|
|
klippel-feil syndrome, autosomal recessive
|
[NCBI]
|
0.000432597
|
|
|
SGM1
|
[NCBI]
|
0.000432597
|
|
|
spondyloepiphyseal dysplasia tarda, toledo type
|
[NCBI]
|
0.000432597
|
|
|
dyssegmental dysplasia, rolland-desbuquois type
|
[NCBI]
|
0.000432597
|
|
|
AOI
|
[NCBI]
|
0.000427595
|
|
|
vater association
|
[NCBI]
|
0.000412223
|
|
|
VDR
|
[NCBI]
|
0.000401519
|
|
|
ALGS1
|
[NCBI]
|
0.000397179
|
|
|
SLE
|
[NCBI]
|
0.000394488
|
|
|
microcephalic osteodysplastic primordial dwarfism, type i
|
[NCBI]
|
0.000379538
|
|
|
opsismodysplasia
|
[NCBI]
|
0.000379538
|
|
|
epiphyseal dysplasia, microcephaly, and nystagmus
|
[NCBI]
|
0.000379538
|
|
|
lateral meningocele syndrome
|
[NCBI]
|
0.000379538
|
|
|
spondyloperipheral dysplasia
|
[NCBI]
|
0.000356322
|
|
|
PPAC
|
[NCBI]
|
0.000341089
|
|
|
fibrochondrogenesis
|
[NCBI]
|
0.000337993
|
|
|
short rib-polydactyly syndrome, type i
|
[NCBI]
|
0.000337993
|
|
|
neuropathy, hereditary motor and sensory, russe type
|
[NCBI]
|
0.000337993
|
|
|
DLL3
|
[NCBI]
|
0.000332569
|
|
|
spondyloocular syndrome, autosomal recessive
|
[NCBI]
|
0.000300811
|
|
|
acroosteolysis with osteoporosis and changes in skull and mandible
|
[NCBI]
|
0.000251035
|
|
|
LRS1
|
[NCBI]
|
0.000228887
|
|
|
CF
|
[NCBI]
|
0.000226876
|
|
|
mucolipidosis iiia
|
[NCBI]
|
0.000223696
|
|
|
pseudodiastrophic dysplasia
|
[NCBI]
|
0.000222536
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
0.000222536
|
|
|
gracile bone dysplasia
|
[NCBI]
|
0.000222536
|
|
|
ACG1A
|
[NCBI]
|
0.000210841
|
|
|
TD1
|
[NCBI]
|
0.000209199
|
|
|
PTH
|
[NCBI]
|
0.000201976
|
|
|
OSCS
|
[NCBI]
|
0.000194048
|
|
|
BMND1
|
[NCBI]
|
0.000182857
|
|
|
acromesomelic dysplasia, hunter-thompson type
|
[NCBI]
|
0.000182857
|
|
|
ACH
|
[NCBI]
|
0.000179947
|
|
|
immunoosseous dysplasia, schimke type
|
[NCBI]
|
0.000166719
|
|
|
FOP
|
[NCBI]
|
0.000165785
|
|
|
rokitansky-kuster-hauser syndrome
|
[NCBI]
|
0.000160154
|
|
|
neural tube defects
|
[NCBI]
|
0.000154301
|
|
|
PAX1
|
[NCBI]
|
0.000150865
|
|
|
lethal short-limb skeletal dysplasia, al gazali type
|
[NCBI]
|
0.000150349
|
|
|
rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunction
|
[NCBI]
|
0.000150349
|
|
|
cholesterol pneumonia
|
[NCBI]
|
0.000150349
|
|
|
polydactyly, postaxial, with dental and vertebral anomalies
|
[NCBI]
|
0.000150349
|
|
|
SCDO2
|
[NCBI]
|
0.000150349
|
|
|
vertebral fusion, posterior lumbosacral, with blepharoptosis
|
[NCBI]
|
0.000150349
|
|
|
cervical vertebral bridge
|
[NCBI]
|
0.000150349
|
|
|
dwarfism with tall vertebrae
|
[NCBI]
|
0.000150349
|
|
|
spinal dysplasia, anhalt type
|
[NCBI]
|
0.000150349
|
|
|
brachyrachia
|
[NCBI]
|
0.000150349
|
|
|
spondyloepiphyseal dysplasia tarda with characteristic facies
|
[NCBI]
|
0.000150349
|
|
|
osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension
|
[NCBI]
|
0.000150349
|
|
|
aphalangy with hemivertebrae
|
[NCBI]
|
0.000150349
|
|
|
spondyloepiphyseal dysplasia, myopia, and sensorineural deafness
|
[NCBI]
|
0.000150349
|
|
|
polydactyly, imperforate anus, and vertebral anomalies
|
[NCBI]
|
0.000150349
|
|
|
spondyloepimetaphyseal dysplasia, micromelic
|
[NCBI]
|
0.000150349
|
|
|
dextrocardia with unusual facies and microphthalmia
|
[NCBI]
|
0.000150349
|
|
|
dyssegmental dysplasia with glaucoma
|
[NCBI]
|
0.000150349
|
|
|
FFS
|
[NCBI]
|
0.000149024
|
|
|
FMD
|
[NCBI]
|
0.000139816
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
0.000131175
|
|
|
chiari malformation type i
|
[NCBI]
|
0.000121604
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
0.000116354
|
|
|
mucopolysaccharidosis type vii
|
[NCBI]
|
0.000111229
|
|
|
neurofibromatosis, familial spinal
|
[NCBI]
|
0.000111213
|
|
|
SCDO3
|
[NCBI]
|
0.000111213
|
|
|
platyspondyly with amelogenesis imperfecta
|
[NCBI]
|
0.000111213
|
|
|
second metatarsal-metacarpal syndrome
|
[NCBI]
|
0.000111213
|
|
|
hydrocephalus, skeletal anomalies, and mental disturbance
|
[NCBI]
|
0.000111213
|
|
|
ulna metaphyseal dysplasia syndrome
|
[NCBI]
|
0.000111213
|
|
|
roifman syndrome
|
[NCBI]
|
0.000111213
|
|
|
larsen-like syndrome, lethal type
|
[NCBI]
|
0.000111213
|
|
|
spondylometaphyseal dysplasia, east african type
|
[NCBI]
|
0.000111213
|
|
|
chondrodysplasia punctata, tibia-metacarpal type
|
[NCBI]
|
0.000111213
|
|
|
BGLAP
|
[NCBI]
|
0.000103065
|
|
|
RSMD1
|
[NCBI]
|
0.000102317
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
9.83963e-05
|
|
|
alopecia-contractures-dwarfism mental retardation syndrome
|
[NCBI]
|
9.65283e-05
|
|
|
osteomesopyknosis
|
[NCBI]
|
9.65283e-05
|
|
|
camptodactyly, tall stature, and hearing loss syndrome
|
[NCBI]
|
9.65283e-05
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
9.65283e-05
|
|
|
spondylolisthesis
|
[NCBI]
|
9.65283e-05
|
|
|
gombo syndrome
|
[NCBI]
|
9.65283e-05
|
|
|
spondylocostal dysostosis with anal atresia and urogenital anomalies
|
[NCBI]
|
9.65283e-05
|
|
|
myeloma, multiple
|
[NCBI]
|
9.65283e-05
|
|
|
spondyloepimetaphyseal dysplasia, type ii
|
[NCBI]
|
9.65283e-05
|
|
|
AOIII
|
[NCBI]
|
9.65283e-05
|
|
|
ENPP1
|
[NCBI]
|
9.35143e-05
|
|
|
isotretinoin embryopathy-like syndrome
|
[NCBI]
|
8.70415e-05
|
|
|
CMT4H
|
[NCBI]
|
8.70415e-05
|
|
|
humerospinal dysostosis
|
[NCBI]
|
8.70415e-05
|
|
|
LFNG
|
[NCBI]
|
8.66093e-05
|
|
|
MBS
|
[NCBI]
|
8.33817e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
8.24872e-05
|
|
|
SMC
|
[NCBI]
|
8.00232e-05
|
|
|
HCA2
|
[NCBI]
|
8.00232e-05
|
|
|
encephalopathy, ethylmalonic
|
[NCBI]
|
8.00232e-05
|
|
|
MLRD
|
[NCBI]
|
8.00232e-05
|
|
|
SMAX1
|
[NCBI]
|
7.7645e-05
|
|
|
MESP2
|
[NCBI]
|
7.53419e-05
|
|
|
enchondromatosis, multiple
|
[NCBI]
|
7.44589e-05
|
|
|
chromosome 18p deletion syndrome
|
[NCBI]
|
7.44589e-05
|
|
|
fibromatosis, gingival, with hypertrichosis
|
[NCBI]
|
7.44589e-05
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
7.44589e-05
|
|
|
OSMED
|
[NCBI]
|
7.44589e-05
|
|
|
keutel syndrome
|
[NCBI]
|
7.44589e-05
|
|
|
avascular necrosis of femoral head, primary
|
[NCBI]
|
7.44589e-05
|
|
|
MCDS
|
[NCBI]
|
7.44589e-05
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
7.44589e-05
|
|
|
boomerang dysplasia
|
[NCBI]
|
7.44589e-05
|
|
|
oeis complex
|
[NCBI]
|
7.44589e-05
|
|
|
FGFR3
|
[NCBI]
|
7.3077e-05
|
|
|
COL2A1
|
[NCBI]
|
7.11505e-05
|
|
|
ACP5
|
[NCBI]
|
7.06647e-05
|
|
|
CMT4B2
|
[NCBI]
|
6.98553e-05
|
|
|
TD2
|
[NCBI]
|
6.59345e-05
|
|
|
CMT4B1
|
[NCBI]
|
6.59345e-05
|
|
|
CMT4C
|
[NCBI]
|
6.59345e-05
|
|
|
FLNB
|
[NCBI]
|
6.53135e-05
|
|
|
HMN2A
|
[NCBI]
|
6.25242e-05
|
|
|
multiple pterygium syndrome, lethal type
|
[NCBI]
|
6.25242e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
6.25242e-05
|
|
|
RNS
|
[NCBI]
|
6.25242e-05
|
|
|
morquio syndrome b
|
[NCBI]
|
6.25242e-05
|
|
|
AMDM
|
[NCBI]
|
6.25242e-05
|
|
|
CMT4D
|
[NCBI]
|
6.25242e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
5.95102e-05
|
|
|
osteoporosis
|
[NCBI]
|
5.95102e-05
|
|
|
DLL1
|
[NCBI]
|
5.76947e-05
|
|
|
SYNS1
|
[NCBI]
|
5.68128e-05
|
|
|
CMT4A
|
[NCBI]
|
5.43742e-05
|
|
|
DMC
|
[NCBI]
|
5.43742e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
5.21808e-05
|
|
|
osteogenesis imperfecta, type iii
|
[NCBI]
|
5.2151e-05
|
|
|
osteogenesis imperfecta, type iv
|
[NCBI]
|
5.2151e-05
|
|
|
currarino syndrome
|
[NCBI]
|
5.011e-05
|
|
|
OPD2
|
[NCBI]
|
5.011e-05
|
|
|
diabetes insipidus, neurohypophyseal type
|
[NCBI]
|
5.011e-05
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
5.011e-05
|
|
|
TNFRSF1B
|
[NCBI]
|
4.9582e-05
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
4.82251e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
4.82251e-05
|
|
|
feingold syndrome
|
[NCBI]
|
4.82251e-05
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
4.82251e-05
|
|
|
GACI
|
[NCBI]
|
4.64755e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
4.48442e-05
|
|
|
poland syndrome
|
[NCBI]
|
4.42278e-05
|
|
|
ATD1
|
[NCBI]
|
4.42278e-05
|
|
|
BCNS
|
[NCBI]
|
4.39816e-05
|
|
|
asplenia with cardiovascular anomalies
|
[NCBI]
|
4.33172e-05
|
|
|
STL1
|
[NCBI]
|
4.1883e-05
|
|
|
mesoderm posterior 1
|
[NCBI]
|
4.14109e-05
|
|
|
MNS
|
[NCBI]
|
4.05317e-05
|
|
|
SEDC
|
[NCBI]
|
4.05317e-05
|
|
|
ESR1
|
[NCBI]
|
3.93059e-05
|
|
|
MKKS
|
[NCBI]
|
3.8046e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
3.8046e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
3.8046e-05
|
|
|
SH3TC2
|
[NCBI]
|
3.76484e-05
|
|
|
PFM
|
[NCBI]
|
3.68984e-05
|
|
|
HOXB8
|
[NCBI]
|
3.5207e-05
|
|
|
NFIX
|
[NCBI]
|
3.5207e-05
|
|
|
TBX18
|
[NCBI]
|
3.5207e-05
|
|
|
BGS
|
[NCBI]
|
3.47665e-05
|
|
|
OKS
|
[NCBI]
|
3.47665e-05
|
|
|
COH1
|
[NCBI]
|
3.37736e-05
|
|
|
CHX10
|
[NCBI]
|
3.3393e-05
|
|
|
NPR2
|
[NCBI]
|
3.3393e-05
|
|
|
GUSB
|
[NCBI]
|
3.33465e-05
|
|
|
FGFR2
|
[NCBI]
|
3.27752e-05
|
|
|
FAM20C
|
[NCBI]
|
3.19486e-05
|
|
|
FDH
|
[NCBI]
|
3.10438e-05
|
|
|
SJS1
|
[NCBI]
|
3.10438e-05
|
|
|
SEPN1
|
[NCBI]
|
3.07485e-05
|
|
|
frank-ter haar syndrome
|
[NCBI]
|
3.07485e-05
|
|
|
NCSTN
|
[NCBI]
|
3.07485e-05
|
|
|
FANCB
|
[NCBI]
|
3.07485e-05
|
|
|
PHS
|
[NCBI]
|
3.02073e-05
|
|
|
XPA
|
[NCBI]
|
3.02073e-05
|
|
|
SIM2
|
[NCBI]
|
2.97218e-05
|
|
|
NOTCH2
|
[NCBI]
|
2.97218e-05
|
|
|
MSD
|
[NCBI]
|
2.94033e-05
|
|
|
LWD
|
[NCBI]
|
2.94033e-05
|
|
|
RCDP1
|
[NCBI]
|
2.86299e-05
|
|
|
NCOR1
|
[NCBI]
|
2.80289e-05
|
|
|
CALCR
|
[NCBI]
|
2.80289e-05
|
|
|
NDRG1
|
[NCBI]
|
2.73132e-05
|
|
|
TLX1
|
[NCBI]
|
2.73132e-05
|
|
|
hypophosphatemic rickets, x-linked dominant
|
[NCBI]
|
2.7167e-05
|
|
|
COL11A2
|
[NCBI]
|
2.66633e-05
|
|
|
AEBP1
|
[NCBI]
|
2.66633e-05
|
|
|
BMI1
|
[NCBI]
|
2.66633e-05
|
|
|
CDX2
|
[NCBI]
|
2.60682e-05
|
|
|
GDAP1
|
[NCBI]
|
2.60682e-05
|
|
|
SHH
|
[NCBI]
|
2.60241e-05
|
|
|
SCS
|
[NCBI]
|
2.58052e-05
|
|
|
ETS2
|
[NCBI]
|
2.55194e-05
|
|
|
MTMR2
|
[NCBI]
|
2.55194e-05
|
|
|
ROR2
|
[NCBI]
|
2.50103e-05
|
|
|
COL10A1
|
[NCBI]
|
2.50103e-05
|
|
|
MMP13
|
[NCBI]
|
2.50103e-05
|
|
|
NF1
|
[NCBI]
|
2.46993e-05
|
|
|
EGF
|
[NCBI]
|
2.44699e-05
|
|
|
FOXC2
|
[NCBI]
|
2.40908e-05
|
|
|
PDGFRA
|
[NCBI]
|
2.36727e-05
|
|
|
EGR2
|
[NCBI]
|
2.36727e-05
|
|
|
PRX
|
[NCBI]
|
2.36727e-05
|
|
|
TRPS2
|
[NCBI]
|
2.33427e-05
|
|
|
CRMO
|
[NCBI]
|
2.33427e-05
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
2.33427e-05
|
|
|
HIP1
|
[NCBI]
|
2.32781e-05
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
2.29046e-05
|
|
|
SRS
|
[NCBI]
|
2.20976e-05
|
|
|
adenylyl cyclase, soluble
|
[NCBI]
|
2.10066e-05
|
|
|
PTHR1
|
[NCBI]
|
2.07353e-05
|
|
|
JAG1
|
[NCBI]
|
2.04742e-05
|
|
|
COL6A1
|
[NCBI]
|
1.998e-05
|
|
|
GDF5
|
[NCBI]
|
1.9519e-05
|
|
|
IGF1
|
[NCBI]
|
1.86809e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
1.86597e-05
|
|
|
CLS
|
[NCBI]
|
1.83555e-05
|
|
|
BPES
|
[NCBI]
|
1.83555e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
1.79295e-05
|
|
|
CHH
|
[NCBI]
|
1.75146e-05
|
|
|
PSACH
|
[NCBI]
|
1.71104e-05
|
|
|
PAX3
|
[NCBI]
|
1.62284e-05
|
|
|
mucolipidosis ii
|
[NCBI]
|
1.59581e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
1.55928e-05
|
|
|
COL1A1
|
[NCBI]
|
1.52151e-05
|
|
|
NOTCH1
|
[NCBI]
|
1.45462e-05
|
|
|
PD
|
[NCBI]
|
1.3228e-05
|
|
|
MAS
|
[NCBI]
|
1.26715e-05
|
|
|
FMF
|
[NCBI]
|
1.21449e-05
|
|
|
CASR
|
[NCBI]
|
1.11749e-05
|
|
|
PTHLH
|
[NCBI]
|
1.00489e-05
|
|
|
STAT1
|
[NCBI]
|
9.51242e-06
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
8.73159e-06
|
|
|
RA
|
[NCBI]
|
8.72816e-06
|
|
|
VEGF
|
[NCBI]
|
8.13017e-06
|
|
|
IHH
|
[NCBI]
|
7.83315e-06
|
|
|
GHR
|
[NCBI]
|
7.69732e-06
|
|
|
TH
|
[NCBI]
|
7.00768e-06
|
|
|
CD
|
[NCBI]
|
5.68123e-06
|
|
|
TNF
|
[NCBI]
|
5.42169e-06
|
|
|
GFAP
|
[NCBI]
|
5.19013e-06
|
|
|
ALB
|
[NCBI]
|
5.17663e-06
|
|
|
FA
|
[NCBI]
|
4.39644e-06
|
|
|
AVP
|
[NCBI]
|
4.26424e-06
|
|
|
COMT
|
[NCBI]
|
2.90548e-06
|
|
|
CTGF
|
[NCBI]
|
2.16031e-06
|
|
|
MFS
|
[NCBI]
|
2.14641e-06
|
|
|
MPO
|
[NCBI]
|
1.99328e-06
|
|
|
EPO
|
[NCBI]
|
1.68651e-06
|
|
|
ACHE
|
[NCBI]
|
9.40852e-07
|
|
|
CEACAM5
|
[NCBI]
|
6.86843e-07
|
|
|
AHR
|
[NCBI]
|
6.62428e-07
|
|
|
GNRH1
|
[NCBI]
|
6.39043e-07
|
|
|
SPP1
|
[NCBI]
|
4.47319e-07
|
|
|
DGS
|
[NCBI]
|
4.39577e-07
|
|
|
AT
|
[NCBI]
|
3.22001e-07
|
|
|
CAT
|
[NCBI]
|
3.15169e-07
|
|
|
CFTR
|
[NCBI]
|
1.65763e-07
|
|
|
KLK3
|
[NCBI]
|
1.56154e-07
|
|
|
temporal arteritis
|
[NCBI]
|
1.0488e-07
|
|
|
HGF
|
[NCBI]
|
8.45813e-08
|
|
|
AFP
|
[NCBI]
|
2.59754e-08
|
|
|
APOE
|
[NCBI]
|
6.44393e-09
|
|
|
CVID
|
[NCBI]
|
4.86298e-09
|
|