|
OMIM |
Link |
Information gain |
01 |
|
chiari malformation type i
|
[NCBI]
|
0.00157791
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.00150788
|
|
|
HFM
|
[NCBI]
|
0.00119466
|
|
|
autism
|
[NCBI]
|
0.0011208
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.00110482
|
|
|
MENOQ1
|
[NCBI]
|
0.000934592
|
|
|
ANON1
|
[NCBI]
|
0.000877227
|
|
|
mammographic density
|
[NCBI]
|
0.000861524
|
|
|
3-@hydroxyisobutyric aciduria
|
[NCBI]
|
0.000861524
|
|
|
theophylline biotransformation
|
[NCBI]
|
0.000861524
|
|
|
amobarbital, deficient n-hydroxylation of
|
[NCBI]
|
0.000861524
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000784736
|
|
|
twinning, dizygotic
|
[NCBI]
|
0.000625691
|
|
|
hypertelorism, microtia, facial clefting syndrome
|
[NCBI]
|
0.000598424
|
|
|
bone size quantitative trait locus 1
|
[NCBI]
|
0.000500438
|
|
|
cerebellar atrophy with progressive microcephaly
|
[NCBI]
|
0.000500438
|
|
|
tune deafness
|
[NCBI]
|
0.000500438
|
|
|
astigmatism
|
[NCBI]
|
0.000500438
|
|
|
BWS
|
[NCBI]
|
0.000467137
|
|
|
twinning, monozygotic
|
[NCBI]
|
0.000450879
|
|
|
fibrochondrogenesis
|
[NCBI]
|
0.000437549
|
|
|
DYX6
|
[NCBI]
|
0.000437549
|
|
|
coronary heart disease, susceptibility to, 2
|
[NCBI]
|
0.000391328
|
|
|
holoprosencephaly
|
[NCBI]
|
0.0003896
|
|
|
corpus callosum, agenesis of, with facial anomalies and robin sequence
|
[NCBI]
|
0.000354925
|
|
|
immunoglobulin m, level of
|
[NCBI]
|
0.000354925
|
|
|
kabuki syndrome
|
[NCBI]
|
0.00034689
|
|
|
MAFD2
|
[NCBI]
|
0.000327888
|
|
|
achalasia, familial esophageal
|
[NCBI]
|
0.000325009
|
|
|
IH
|
[NCBI]
|
0.000325009
|
|
|
cluster headache, familial
|
[NCBI]
|
0.000325009
|
|
|
MNG1
|
[NCBI]
|
0.000325009
|
|
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.000318896
|
|
|
DMD
|
[NCBI]
|
0.000317225
|
|
|
RA
|
[NCBI]
|
0.000302594
|
|
|
gastroesophageal reflux
|
[NCBI]
|
0.000299704
|
|
|
CF
|
[NCBI]
|
0.00029276
|
|
|
wernicke-korsakoff syndrome
|
[NCBI]
|
0.000277847
|
|
|
FSHMD1A
|
[NCBI]
|
0.000264896
|
|
|
centralopathic epilepsy
|
[NCBI]
|
0.000258666
|
|
|
BULN1
|
[NCBI]
|
0.000258666
|
|
|
WM1
|
[NCBI]
|
0.000258666
|
|
|
ETL2
|
[NCBI]
|
0.000226328
|
|
|
mast cell disease
|
[NCBI]
|
0.00021503
|
|
|
dystonia, juvenile-onset
|
[NCBI]
|
0.000213663
|
|
|
neuronal intranuclear inclusion disease
|
[NCBI]
|
0.000213663
|
|
|
OFC1
|
[NCBI]
|
0.000203158
|
|
|
AIC
|
[NCBI]
|
0.000188322
|
|
|
PAND1
|
[NCBI]
|
0.000188322
|
|
|
alopecia areata 1
|
[NCBI]
|
0.000188322
|
|
|
MS
|
[NCBI]
|
0.000184095
|
|
|
RSTS
|
[NCBI]
|
0.000168517
|
|
|
caudal duplication anomaly
|
[NCBI]
|
0.000158309
|
|
|
SRS
|
[NCBI]
|
0.000154033
|
|
|
aromatic l-amino acid decarboxylase deficiency
|
[NCBI]
|
0.000146536
|
|
|
JBTS1
|
[NCBI]
|
0.000142237
|
|
|
LIP
|
[NCBI]
|
0.000141445
|
|
|
SCDO1
|
[NCBI]
|
0.000141445
|
|
|
EHBA
|
[NCBI]
|
0.000137536
|
|
|
oeis complex
|
[NCBI]
|
0.000137536
|
|
|
DYX1
|
[NCBI]
|
0.000136513
|
|
|
TD1
|
[NCBI]
|
0.000135997
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.0001278
|
|
|
CPI
|
[NCBI]
|
0.000124579
|
|
|
IDD
|
[NCBI]
|
0.000124115
|
|
|
breast cancer
|
[NCBI]
|
0.000123562
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
0.000116887
|
|
|
GBD1
|
[NCBI]
|
0.000114184
|
|
|
myeloma, multiple
|
[NCBI]
|
0.000110043
|
|
|
osteochondrosis deformans tibiae, familial infantile type
|
[NCBI]
|
0.000106803
|
|
|
folate level in erythrocytes
|
[NCBI]
|
0.000106803
|
|
|
colonic atresia
|
[NCBI]
|
0.000106803
|
|
|
dysphasia, familial developmental
|
[NCBI]
|
0.000106803
|
|
|
bile duct cysts
|
[NCBI]
|
0.000106803
|
|
|
lip prints
|
[NCBI]
|
0.000106803
|
|
|
subependymoma
|
[NCBI]
|
0.000106803
|
|
|
facial dysmorphism, selective tooth agenesis, and choroid calcification
|
[NCBI]
|
0.000106803
|
|
|
myoclonus, cerebellar ataxia, and deafness
|
[NCBI]
|
0.000106803
|
|
|
PPAB
|
[NCBI]
|
0.000106803
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
0.000102911
|
|
|
FRNS
|
[NCBI]
|
9.84139e-05
|
|
|
HMS1
|
[NCBI]
|
9.69151e-05
|
|
|
bare lymphocyte syndrome, type ii
|
[NCBI]
|
9.23412e-05
|
|
|
HD
|
[NCBI]
|
8.88909e-05
|
|
|
SLE
|
[NCBI]
|
8.46014e-05
|
|
|
DWS
|
[NCBI]
|
8.42705e-05
|
|
|
ETM1
|
[NCBI]
|
8.31868e-05
|
|
|
lithium transport
|
[NCBI]
|
7.91262e-05
|
|
|
acne, adult
|
[NCBI]
|
7.91262e-05
|
|
|
arachnoid cysts, intracranial
|
[NCBI]
|
7.91262e-05
|
|
|
colchicine resistance
|
[NCBI]
|
7.91262e-05
|
|
|
periodontitis, chronic
|
[NCBI]
|
7.91262e-05
|
|
|
craniosynostosis with ectopia lentis
|
[NCBI]
|
7.91262e-05
|
|
|
langerhans cell histiocytosis
|
[NCBI]
|
7.91262e-05
|
|
|
osteoporosis
|
[NCBI]
|
7.7873e-05
|
|
|
lung cancer
|
[NCBI]
|
7.47236e-05
|
|
|
RTT
|
[NCBI]
|
6.96127e-05
|
|
|
NRCLP1
|
[NCBI]
|
6.9161e-05
|
|
|
tracheobronchial stenosis, congenital
|
[NCBI]
|
6.87401e-05
|
|
|
HSAN5
|
[NCBI]
|
6.87401e-05
|
|
|
ovarian teratoma
|
[NCBI]
|
6.87401e-05
|
|
|
say syndrome
|
[NCBI]
|
6.87401e-05
|
|
|
coloboma of optic nerve
|
[NCBI]
|
6.87401e-05
|
|
|
bile acid synthesis defect, congenital, 2
|
[NCBI]
|
6.87401e-05
|
|
|
androstenone, ability to smell
|
[NCBI]
|
6.87401e-05
|
|
|
rokitansky-kuster-hauser syndrome
|
[NCBI]
|
6.87401e-05
|
|
|
sodium-potassium-atpase activity of red cell
|
[NCBI]
|
6.87401e-05
|
|
|
barraquer-simons syndrome
|
[NCBI]
|
6.87401e-05
|
|
|
keratitis, hereditary
|
[NCBI]
|
6.87401e-05
|
|
|
aprosencephaly syndrome
|
[NCBI]
|
6.87401e-05
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
6.84477e-05
|
|
|
AXIN1
|
[NCBI]
|
6.52743e-05
|
|
|
CDLS1
|
[NCBI]
|
6.37515e-05
|
|
|
EEG
|
[NCBI]
|
6.20294e-05
|
|
|
hair whorl
|
[NCBI]
|
6.20294e-05
|
|
|
brachydactyly-ectrodactyly with fibular aplasia or hypoplasia
|
[NCBI]
|
6.20294e-05
|
|
|
tongue curling, folding, or rolling
|
[NCBI]
|
6.20294e-05
|
|
|
goodpasture syndrome
|
[NCBI]
|
6.20294e-05
|
|
|
oncocytoma
|
[NCBI]
|
6.20294e-05
|
|
|
femur-fibula-ulna syndrome
|
[NCBI]
|
6.20294e-05
|
|
|
atrioventricular conduction time
|
[NCBI]
|
6.20294e-05
|
|
|
respiratory underresponsiveness to hypoxia and hypercapnia
|
[NCBI]
|
6.20294e-05
|
|
|
hand clasping pattern
|
[NCBI]
|
6.20294e-05
|
|
|
FMR1
|
[NCBI]
|
6.1923e-05
|
|
|
PPR
|
[NCBI]
|
6.16078e-05
|
|
|
CDG1A
|
[NCBI]
|
6.11721e-05
|
|
|
EPHX2
|
[NCBI]
|
6.04278e-05
|
|
|
PCOS1
|
[NCBI]
|
5.84205e-05
|
|
|
SMEI
|
[NCBI]
|
5.82546e-05
|
|
|
lichen planus, familial
|
[NCBI]
|
5.70643e-05
|
|
|
respiratory distress syndrome in premature infants
|
[NCBI]
|
5.70643e-05
|
|
|
TINU
|
[NCBI]
|
5.70643e-05
|
|
|
ACTB
|
[NCBI]
|
5.4352e-05
|
|
|
sotos syndrome
|
[NCBI]
|
5.39043e-05
|
|
|
OCA1B
|
[NCBI]
|
5.31273e-05
|
|
|
nonarteritic anterior ischemic optic neuropathy, susceptibility to
|
[NCBI]
|
5.31273e-05
|
|
|
gastroschisis
|
[NCBI]
|
5.31273e-05
|
|
|
creatine phosphokinase, elevated serum
|
[NCBI]
|
5.31273e-05
|
|
|
HPE4
|
[NCBI]
|
5.31273e-05
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
5.24704e-05
|
|
|
GTS
|
[NCBI]
|
5.06687e-05
|
|
|
TD2
|
[NCBI]
|
4.98696e-05
|
|
|
pneumothorax, primary spontaneous
|
[NCBI]
|
4.98696e-05
|
|
|
FHL2
|
[NCBI]
|
4.98696e-05
|
|
|
HSR
|
[NCBI]
|
4.87813e-05
|
|
|
IS1
|
[NCBI]
|
4.83506e-05
|
|
|
VWS
|
[NCBI]
|
4.73178e-05
|
|
|
OPLL
|
[NCBI]
|
4.70948e-05
|
|
|
takayasu arteritis
|
[NCBI]
|
4.70948e-05
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
4.70385e-05
|
|
|
EIG
|
[NCBI]
|
4.54595e-05
|
|
|
RHN
|
[NCBI]
|
4.4681e-05
|
|
|
tobacco addiction, susceptibility to
|
[NCBI]
|
4.4681e-05
|
|
|
macular dystrophy, vitelliform, adult-onset
|
[NCBI]
|
4.4681e-05
|
|
|
SHBG
|
[NCBI]
|
4.34996e-05
|
|
|
NETH
|
[NCBI]
|
4.25474e-05
|
|
|
WZS
|
[NCBI]
|
4.25474e-05
|
|
|
aryl hydrocarbon hydroxylase inducibility
|
[NCBI]
|
4.25474e-05
|
|
|
hematopoietic stem cell kinetics, control of
|
[NCBI]
|
4.25474e-05
|
|
|
SVAS
|
[NCBI]
|
4.24591e-05
|
|
|
CYP1A1
|
[NCBI]
|
4.24492e-05
|
|
|
HPE2
|
[NCBI]
|
3.89108e-05
|
|
|
SHEP1
|
[NCBI]
|
3.73364e-05
|
|
|
BMND1
|
[NCBI]
|
3.73364e-05
|
|
|
OPPG
|
[NCBI]
|
3.73364e-05
|
|
|
heart block, congenital
|
[NCBI]
|
3.73364e-05
|
|
|
acyl-coa dehydrogenase, short-chain, deficiency of
|
[NCBI]
|
3.73364e-05
|
|
|
parkinson disease, mitochondrial
|
[NCBI]
|
3.73364e-05
|
|
|
PI
|
[NCBI]
|
3.66738e-05
|
|
|
PPS
|
[NCBI]
|
3.58908e-05
|
|
|
SCZD9
|
[NCBI]
|
3.58908e-05
|
|
|
BHD
|
[NCBI]
|
3.58908e-05
|
|
|
ADLTE
|
[NCBI]
|
3.45556e-05
|
|
|
aging
|
[NCBI]
|
3.45556e-05
|
|
|
CFTD
|
[NCBI]
|
3.45556e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
3.45556e-05
|
|
|
HPE3
|
[NCBI]
|
3.45556e-05
|
|
|
AD
|
[NCBI]
|
3.41215e-05
|
|
|
kiaa0442
|
[NCBI]
|
3.37088e-05
|
|
|
ST3GAL6
|
[NCBI]
|
3.37088e-05
|
|
|
PFM
|
[NCBI]
|
3.33161e-05
|
|
|
CSID
|
[NCBI]
|
3.33161e-05
|
|
|
helicobacter pylori infection, susceptibility to
|
[NCBI]
|
3.33161e-05
|
|
|
VDR
|
[NCBI]
|
3.32967e-05
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
3.29945e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
3.29729e-05
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
3.21602e-05
|
|
|
longevity
|
[NCBI]
|
3.21602e-05
|
|
|
thyroid hormonogenesis, genetic defect in, 2a
|
[NCBI]
|
3.21602e-05
|
|
|
RSMD1
|
[NCBI]
|
3.21602e-05
|
|
|
LEPR
|
[NCBI]
|
3.21431e-05
|
|
|
MAS
|
[NCBI]
|
3.18664e-05
|
|
|
TSNAX
|
[NCBI]
|
3.16902e-05
|
|
|
ACTG2
|
[NCBI]
|
3.16902e-05
|
|
|
BGS
|
[NCBI]
|
3.10781e-05
|
|
|
OFD1
|
[NCBI]
|
3.10781e-05
|
|
|
APOB
|
[NCBI]
|
3.04794e-05
|
|
|
GLS
|
[NCBI]
|
3.019e-05
|
|
|
BFLS
|
[NCBI]
|
3.00615e-05
|
|
|
stroke, ischemic
|
[NCBI]
|
2.91037e-05
|
|
|
mucopolysaccharidosis type iiib
|
[NCBI]
|
2.91037e-05
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
2.91037e-05
|
|
|
polycythemia vera
|
[NCBI]
|
2.91037e-05
|
|
|
ACE
|
[NCBI]
|
2.85612e-05
|
|
|
krabbe disease
|
[NCBI]
|
2.83283e-05
|
|
|
EDMD2
|
[NCBI]
|
2.81986e-05
|
|
|
aortic aneurysm, abdominal
|
[NCBI]
|
2.73413e-05
|
|
|
pulmonary fibrosis, idiopathic
|
[NCBI]
|
2.73413e-05
|
|
|
fraser syndrome
|
[NCBI]
|
2.73413e-05
|
|
|
ADHD
|
[NCBI]
|
2.70461e-05
|
|
|
VHL
|
[NCBI]
|
2.67362e-05
|
|
|
CHNG2
|
[NCBI]
|
2.65274e-05
|
|
|
hodgkin lymphoma
|
[NCBI]
|
2.65274e-05
|
|
|
sudden infant death syndrome
|
[NCBI]
|
2.65274e-05
|
|
|
ALD
|
[NCBI]
|
2.58579e-05
|
|
|
AMT
|
[NCBI]
|
2.57502e-05
|
|
|
CFD
|
[NCBI]
|
2.51573e-05
|
|
|
GYS1
|
[NCBI]
|
2.51573e-05
|
|
|
MG
|
[NCBI]
|
2.51338e-05
|
|
|
MRXHF1
|
[NCBI]
|
2.50152e-05
|
|
|
charge syndrome
|
[NCBI]
|
2.50152e-05
|
|
|
ZNF9
|
[NCBI]
|
2.46188e-05
|
|
|
RFX5
|
[NCBI]
|
2.46188e-05
|
|
|
osteoarthritis
|
[NCBI]
|
2.43107e-05
|
|
|
LCA1
|
[NCBI]
|
2.43107e-05
|
|
|
SULT1A1
|
[NCBI]
|
2.41255e-05
|
|
|
SFTPD
|
[NCBI]
|
2.41255e-05
|
|
|
RNR1
|
[NCBI]
|
2.32481e-05
|
|
|
SPDA1
|
[NCBI]
|
2.29919e-05
|
|
|
HSAS
|
[NCBI]
|
2.29919e-05
|
|
|
NAGLU
|
[NCBI]
|
2.28542e-05
|
|
|
IRF6
|
[NCBI]
|
2.24852e-05
|
|
|
CYP1A2
|
[NCBI]
|
2.24852e-05
|
|
|
mycobacterium tuberculosis, susceptibility to
|
[NCBI]
|
2.23734e-05
|
|
|
testicular tumors
|
[NCBI]
|
2.23734e-05
|
|
|
KCNQ1OT1
|
[NCBI]
|
2.21381e-05
|
|
|
FGB
|
[NCBI]
|
2.21381e-05
|
|
|
RBS
|
[NCBI]
|
2.12086e-05
|
|
|
SGBS1
|
[NCBI]
|
2.06593e-05
|
|
|
SCN1A
|
[NCBI]
|
1.96963e-05
|
|
|
CMD1A
|
[NCBI]
|
1.96201e-05
|
|
|
ALDH1A1
|
[NCBI]
|
1.9479e-05
|
|
|
PCTT
|
[NCBI]
|
1.91279e-05
|
|
|
SJS1
|
[NCBI]
|
1.91279e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
1.91279e-05
|
|
|
ETV6
|
[NCBI]
|
1.88721e-05
|
|
|
DISC1
|
[NCBI]
|
1.88721e-05
|
|
|
GCDH
|
[NCBI]
|
1.86831e-05
|
|
|
GCPS
|
[NCBI]
|
1.86525e-05
|
|
|
kartagener syndrome
|
[NCBI]
|
1.86525e-05
|
|
|
malaria, susceptibility to
|
[NCBI]
|
1.86525e-05
|
|
|
CETP
|
[NCBI]
|
1.85002e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
1.85002e-05
|
|
|
COH1
|
[NCBI]
|
1.8193e-05
|
|
|
CBD
|
[NCBI]
|
1.7984e-05
|
|
|
PIGA
|
[NCBI]
|
1.78218e-05
|
|
|
ALDH2
|
[NCBI]
|
1.75105e-05
|
|
|
JAG1
|
[NCBI]
|
1.7361e-05
|
|
|
EDN1
|
[NCBI]
|
1.70732e-05
|
|
|
POAG
|
[NCBI]
|
1.69018e-05
|
|
|
HLA-DRA
|
[NCBI]
|
1.67992e-05
|
|
|
ADIPOQ
|
[NCBI]
|
1.66671e-05
|
|
|
LPA
|
[NCBI]
|
1.66671e-05
|
|
|
IGER
|
[NCBI]
|
1.64979e-05
|
|
|
KAL1
|
[NCBI]
|
1.64116e-05
|
|
|
COL7A1
|
[NCBI]
|
1.60487e-05
|
|
|
LI1
|
[NCBI]
|
1.57264e-05
|
|
|
DM2
|
[NCBI]
|
1.53576e-05
|
|
|
F2
|
[NCBI]
|
1.50822e-05
|
|
|
REN
|
[NCBI]
|
1.50822e-05
|
|
|
ALGS1
|
[NCBI]
|
1.49993e-05
|
|
|
MTND4
|
[NCBI]
|
1.47009e-05
|
|
|
FA
|
[NCBI]
|
1.46615e-05
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
1.46095e-05
|
|
|
BIRC1
|
[NCBI]
|
1.4344e-05
|
|
|
CSA
|
[NCBI]
|
1.43127e-05
|
|
|
TGFB1
|
[NCBI]
|
1.42582e-05
|
|
|
IL10
|
[NCBI]
|
1.38483e-05
|
|
|
TSC2
|
[NCBI]
|
1.37699e-05
|
|
|
obesity
|
[NCBI]
|
1.36632e-05
|
|
|
HNPP
|
[NCBI]
|
1.36632e-05
|
|
|
TNF
|
[NCBI]
|
1.34957e-05
|
|
|
VEGF
|
[NCBI]
|
1.33898e-05
|
|
|
OCP
|
[NCBI]
|
1.33515e-05
|
|
|
WBS
|
[NCBI]
|
1.31106e-05
|
|
|
HRG
|
[NCBI]
|
1.311e-05
|
|
|
BTK
|
[NCBI]
|
1.25214e-05
|
|
|
ED1
|
[NCBI]
|
1.2464e-05
|
|
|
GH1
|
[NCBI]
|
1.18795e-05
|
|
|
ARMD1
|
[NCBI]
|
1.13813e-05
|
|
|
COMT
|
[NCBI]
|
1.09563e-05
|
|
|
IGFALS
|
[NCBI]
|
1.05279e-05
|
|
|
DDC
|
[NCBI]
|
1.01983e-05
|
|
|
FTD
|
[NCBI]
|
9.74549e-06
|
|
|
LEP
|
[NCBI]
|
9.38816e-06
|
|
|
CMT1A
|
[NCBI]
|
9.2942e-06
|
|
|
hemophilia a
|
[NCBI]
|
8.96438e-06
|
|
|
FMF
|
[NCBI]
|
8.6993e-06
|
|
|
IDDM
|
[NCBI]
|
8.57481e-06
|
|
|
COMP
|
[NCBI]
|
7.87683e-06
|
|
|
APRT
|
[NCBI]
|
6.99313e-06
|
|
|
MDD
|
[NCBI]
|
5.89577e-06
|
|
|
MBL2
|
[NCBI]
|
5.54928e-06
|
|
|
APOE
|
[NCBI]
|
5.54404e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
5.21466e-06
|
|
|
WT1
|
[NCBI]
|
5.12297e-06
|
|
|
SCA1
|
[NCBI]
|
4.76817e-06
|
|
|
PD
|
[NCBI]
|
4.20418e-06
|
|
|
MB
|
[NCBI]
|
4.14175e-06
|
|
|
SCZD
|
[NCBI]
|
4.118e-06
|
|
|
TS
|
[NCBI]
|
4.08471e-06
|
|
|
hypercholesterolemia, autosomal dominant
|
[NCBI]
|
3.82028e-06
|
|
|
ACP5
|
[NCBI]
|
2.89288e-06
|
|
|
KSS
|
[NCBI]
|
2.71343e-06
|
|
|
NPY
|
[NCBI]
|
2.4793e-06
|
|
|
PCD
|
[NCBI]
|
2.3576e-06
|
|
|
LPL
|
[NCBI]
|
2.15239e-06
|
|
|
TTR
|
[NCBI]
|
1.96684e-06
|
|
|
PMD
|
[NCBI]
|
1.63732e-06
|
|
|
MBP
|
[NCBI]
|
1.60857e-06
|
|
|
TH
|
[NCBI]
|
1.23462e-06
|
|
|
AVP
|
[NCBI]
|
1.20738e-06
|
|
|
DRPLA
|
[NCBI]
|
9.62661e-07
|
|
|
AIS
|
[NCBI]
|
9.25457e-07
|
|
|
AR
|
[NCBI]
|
8.76667e-07
|
|
|
WAS
|
[NCBI]
|
7.77428e-07
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
6.00911e-07
|
|
|
PJS
|
[NCBI]
|
5.45801e-07
|
|
|
CEACAM5
|
[NCBI]
|
5.24929e-07
|
|
|
PTH
|
[NCBI]
|
4.5719e-07
|
|
|
CD
|
[NCBI]
|
3.9674e-07
|
|
|
PRL
|
[NCBI]
|
3.65669e-07
|
|
|
EPO
|
[NCBI]
|
2.99155e-07
|
|
|
DGS
|
[NCBI]
|
2.77259e-07
|
|
|
leber optic atrophy
|
[NCBI]
|
1.94525e-07
|
|
|
AFP
|
[NCBI]
|
7.37228e-08
|
|
|
ACHE
|
[NCBI]
|
4.92841e-08
|
|
|
GIST
|
[NCBI]
|
3.16146e-08
|
|
|
NPPA
|
[NCBI]
|
2.97787e-08
|
|
|
MODY
|
[NCBI]
|
2.14937e-08
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.7331e-08
|
|
|
CFTR
|
[NCBI]
|
6.28875e-10
|
|