|
OMIM |
Link |
Information gain |
01 |
|
FTD
|
[NCBI]
|
0.00246555
|
|
|
DRPLA
|
[NCBI]
|
0.0023397
|
|
|
chorioretinal atrophy, progressive bifocal
|
[NCBI]
|
0.00203177
|
|
|
BZX
|
[NCBI]
|
0.00199147
|
|
|
cataract, congenital, with mental impairment and dentate gyrus atrophy
|
[NCBI]
|
0.00158695
|
|
|
diarrhea 2, with microvillous atrophy
|
[NCBI]
|
0.00137889
|
|
|
AD
|
[NCBI]
|
0.00133269
|
|
|
RA
|
[NCBI]
|
0.00128967
|
|
|
glaucoma-related pigment dispersion syndrome
|
[NCBI]
|
0.00118322
|
|
|
CORD7
|
[NCBI]
|
0.00106087
|
|
|
chorioretinal dystrophy, spinocerebellar ataxia, and hypogonadotropic hypogonadism
|
[NCBI]
|
0.000933496
|
|
|
spinocerebellar ataxia 29
|
[NCBI]
|
0.000808172
|
|
|
striae distensae, familial
|
[NCBI]
|
0.00079215
|
|
|
DYTCA
|
[NCBI]
|
0.00079215
|
|
|
SPAX3
|
[NCBI]
|
0.00079215
|
|
|
MCOPS10
|
[NCBI]
|
0.00079215
|
|
|
epilepsy, myoclonic, benign adult familial, type 1
|
[NCBI]
|
0.000720421
|
|
|
CACD
|
[NCBI]
|
0.000575205
|
|
|
brachial palsy, familial congenital
|
[NCBI]
|
0.000575205
|
|
|
CPD2
|
[NCBI]
|
0.000575205
|
|
|
polymicrogyria, unilateral
|
[NCBI]
|
0.000575205
|
|
|
PPCRA
|
[NCBI]
|
0.00057164
|
|
|
ornithine aminotransferase deficiency
|
[NCBI]
|
0.000544498
|
|
|
CF
|
[NCBI]
|
0.000520477
|
|
|
MJD
|
[NCBI]
|
0.000517368
|
|
|
pontocerebellar hypoplasia, type 2
|
[NCBI]
|
0.000493952
|
|
|
macrocephaly with multiple epiphyseal dysplasia and distinctive facies
|
[NCBI]
|
0.000493952
|
|
|
behr syndrome
|
[NCBI]
|
0.000493952
|
|
|
SCAR6
|
[NCBI]
|
0.000493952
|
|
|
CD
|
[NCBI]
|
0.00047339
|
|
|
spinal muscular atrophy, facioscapulohumeral type
|
[NCBI]
|
0.000441541
|
|
|
FPLD1
|
[NCBI]
|
0.000441541
|
|
|
CMT2B2
|
[NCBI]
|
0.000441541
|
|
|
malignant atrophic papulosis
|
[NCBI]
|
0.000372187
|
|
|
IOSCA
|
[NCBI]
|
0.000372187
|
|
|
cerebellar ataxia and hypogonadotropic hypogonadism
|
[NCBI]
|
0.000346875
|
|
|
peho syndrome
|
[NCBI]
|
0.000346875
|
|
|
wernicke-korsakoff syndrome
|
[NCBI]
|
0.000346875
|
|
|
sclerotylosis
|
[NCBI]
|
0.000346875
|
|
|
SLE
|
[NCBI]
|
0.00034358
|
|
|
CLN4A
|
[NCBI]
|
0.000325352
|
|
|
microcephaly, hiatus hernia, and nephrotic syndrome
|
[NCBI]
|
0.000306663
|
|
|
immune defect due to absence of thymus
|
[NCBI]
|
0.000306663
|
|
|
carnitine deficiency, myopathic
|
[NCBI]
|
0.000306663
|
|
|
DRPLA
|
[NCBI]
|
0.000292545
|
|
|
spinal muscular atrophy, childhood, proximal, autosomal dominant
|
[NCBI]
|
0.000290172
|
|
|
amyotrophy, monomelic
|
[NCBI]
|
0.000290172
|
|
|
HD
|
[NCBI]
|
0.000264779
|
|
|
renal failure, progressive, with hypertension
|
[NCBI]
|
0.000262141
|
|
|
MYMY1
|
[NCBI]
|
0.00025004
|
|
|
FXTAS
|
[NCBI]
|
0.000242492
|
|
|
WDM
|
[NCBI]
|
0.000228725
|
|
|
SCA1
|
[NCBI]
|
0.000211151
|
|
|
LSA
|
[NCBI]
|
0.000210981
|
|
|
APOE
|
[NCBI]
|
0.000200247
|
|
|
SCA2
|
[NCBI]
|
0.000195895
|
|
|
MCDR1
|
[NCBI]
|
0.000187211
|
|
|
SCA7
|
[NCBI]
|
0.00018433
|
|
|
SCRA
|
[NCBI]
|
0.00017772
|
|
|
IBGC1
|
[NCBI]
|
0.00017389
|
|
|
AMVC
|
[NCBI]
|
0.000163186
|
|
|
PPAB
|
[NCBI]
|
0.000163186
|
|
|
AGS1
|
[NCBI]
|
0.00016252
|
|
|
GLUD1
|
[NCBI]
|
0.000159697
|
|
|
EAOH
|
[NCBI]
|
0.00015622
|
|
|
CJD
|
[NCBI]
|
0.000144402
|
|
|
FRNS
|
[NCBI]
|
0.000132284
|
|
|
COL17A1
|
[NCBI]
|
0.000124832
|
|
|
acrogeria, gottron type
|
[NCBI]
|
0.000118453
|
|
|
PCNA
|
[NCBI]
|
0.000118355
|
|
|
poland syndrome
|
[NCBI]
|
0.000116362
|
|
|
pick disease of brain
|
[NCBI]
|
0.000114936
|
|
|
glutaric acidemia i
|
[NCBI]
|
0.000112173
|
|
|
CMTC
|
[NCBI]
|
0.000110608
|
|
|
SCA17
|
[NCBI]
|
0.000104779
|
|
|
basal ganglia disease, adult-onset
|
[NCBI]
|
0.0001017
|
|
|
gliosis, familial progressive subcortical
|
[NCBI]
|
0.0001017
|
|
|
myoclonic epilepsy of unverricht and lundborg
|
[NCBI]
|
0.000100614
|
|
|
GCDH
|
[NCBI]
|
8.77863e-05
|
|
|
MSS
|
[NCBI]
|
8.64899e-05
|
|
|
FTD3
|
[NCBI]
|
8.29145e-05
|
|
|
neurologic disease, infantile multisystem, with osseous fragility
|
[NCBI]
|
8.15793e-05
|
|
|
muscular dystrophy, congenital, with cerebellar atrophy
|
[NCBI]
|
8.15793e-05
|
|
|
follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts
|
[NCBI]
|
8.15793e-05
|
|
|
diarrhea, chronic, with villous atrophy
|
[NCBI]
|
8.15793e-05
|
|
|
motor neuron disease with dementia and ophthalmoplegia
|
[NCBI]
|
8.15793e-05
|
|
|
encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts
|
[NCBI]
|
8.15793e-05
|
|
|
laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy
|
[NCBI]
|
8.15793e-05
|
|
|
SCAR1
|
[NCBI]
|
7.95917e-05
|
|
|
APC
|
[NCBI]
|
7.50196e-05
|
|
|
STGD3
|
[NCBI]
|
7.38757e-05
|
|
|
MAPT
|
[NCBI]
|
7.35811e-05
|
|
|
ALD
|
[NCBI]
|
7.18177e-05
|
|
|
ELOVL4
|
[NCBI]
|
7.17418e-05
|
|
|
myoclonic epilepsy, neonatal, with suppression-burst pattern
|
[NCBI]
|
7.13808e-05
|
|
|
SPS
|
[NCBI]
|
7.12755e-05
|
|
|
SFD
|
[NCBI]
|
6.90796e-05
|
|
|
VRNI
|
[NCBI]
|
6.50869e-05
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
6.30934e-05
|
|
|
VEGF
|
[NCBI]
|
6.26015e-05
|
|
|
FTLDU
|
[NCBI]
|
6.1344e-05
|
|
|
MAP3K7IP1
|
[NCBI]
|
6.06385e-05
|
|
|
IPO8
|
[NCBI]
|
6.06385e-05
|
|
|
PD
|
[NCBI]
|
6.02368e-05
|
|
|
ataxia-microcephaly-cataract syndrome
|
[NCBI]
|
5.92126e-05
|
|
|
OPCA V
|
[NCBI]
|
5.92126e-05
|
|
|
retinopathy, pericentral pigmentary, dominant
|
[NCBI]
|
5.92126e-05
|
|
|
cerebellar ataxia and hypergonadotropic hypogonadism
|
[NCBI]
|
5.92126e-05
|
|
|
microcephalic primordial dwarfism, toriello type
|
[NCBI]
|
5.92126e-05
|
|
|
cerebellar ataxia, deafness, and narcolepsy
|
[NCBI]
|
5.92126e-05
|
|
|
choroid plexus calcification and mental retardation
|
[NCBI]
|
5.92126e-05
|
|
|
retinopathy, pericentral pigmentary, autosomal recessive
|
[NCBI]
|
5.92126e-05
|
|
|
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis
|
[NCBI]
|
5.92126e-05
|
|
|
DDD
|
[NCBI]
|
5.66594e-05
|
|
|
AHR
|
[NCBI]
|
5.66328e-05
|
|
|
PTH
|
[NCBI]
|
5.56296e-05
|
|
|
GABEB
|
[NCBI]
|
5.52559e-05
|
|
|
canavan disease
|
[NCBI]
|
5.26447e-05
|
|
|
CLN1
|
[NCBI]
|
5.14263e-05
|
|
|
microcephaly, corpus callosum dysgenesis, and cleft lip/palate
|
[NCBI]
|
5.08364e-05
|
|
|
muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers
|
[NCBI]
|
5.08364e-05
|
|
|
BDNF
|
[NCBI]
|
4.92096e-05
|
|
|
STGD1
|
[NCBI]
|
4.80679e-05
|
|
|
TSNAX
|
[NCBI]
|
4.68801e-05
|
|
|
DIO1
|
[NCBI]
|
4.68801e-05
|
|
|
BOLL
|
[NCBI]
|
4.68801e-05
|
|
|
TAF4
|
[NCBI]
|
4.68801e-05
|
|
|
MTATP8
|
[NCBI]
|
4.68801e-05
|
|
|
polyposis, skin pigmentation, alopecia, and fingernail changes
|
[NCBI]
|
4.54341e-05
|
|
|
haw river syndrome
|
[NCBI]
|
4.54341e-05
|
|
|
CLN10
|
[NCBI]
|
4.54341e-05
|
|
|
SPG7
|
[NCBI]
|
4.54341e-05
|
|
|
MADB
|
[NCBI]
|
4.54341e-05
|
|
|
ASPA
|
[NCBI]
|
4.47417e-05
|
|
|
SMAX1
|
[NCBI]
|
4.42648e-05
|
|
|
GIP
|
[NCBI]
|
4.26915e-05
|
|
|
GPNMB
|
[NCBI]
|
4.17009e-05
|
|
|
PCM1
|
[NCBI]
|
4.17009e-05
|
|
|
RNF28
|
[NCBI]
|
4.17009e-05
|
|
|
SCA15
|
[NCBI]
|
4.14441e-05
|
|
|
barber-say syndrome
|
[NCBI]
|
4.14441e-05
|
|
|
CEACAM5
|
[NCBI]
|
4.14272e-05
|
|
|
CHAC
|
[NCBI]
|
4.0764e-05
|
|
|
CDPX2
|
[NCBI]
|
4.0764e-05
|
|
|
CADASIL
|
[NCBI]
|
3.99813e-05
|
|
|
SPG3A
|
[NCBI]
|
3.84859e-05
|
|
|
CTF1
|
[NCBI]
|
3.83453e-05
|
|
|
NFAT5
|
[NCBI]
|
3.83453e-05
|
|
|
PITPN
|
[NCBI]
|
3.83453e-05
|
|
|
COQ2
|
[NCBI]
|
3.83453e-05
|
|
|
NHLH2
|
[NCBI]
|
3.83453e-05
|
|
|
azoospermia due to perturbations of meiosis
|
[NCBI]
|
3.8286e-05
|
|
|
HDL1
|
[NCBI]
|
3.8286e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
3.64521e-05
|
|
|
DPYS
|
[NCBI]
|
3.58559e-05
|
|
|
PDC
|
[NCBI]
|
3.58559e-05
|
|
|
RB1CC1
|
[NCBI]
|
3.58559e-05
|
|
|
SMAD7
|
[NCBI]
|
3.58559e-05
|
|
|
GJD2
|
[NCBI]
|
3.58559e-05
|
|
|
cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome
|
[NCBI]
|
3.56776e-05
|
|
|
3-@methylglutaconic aciduria, type iii
|
[NCBI]
|
3.56776e-05
|
|
|
ALS4
|
[NCBI]
|
3.56776e-05
|
|
|
sulfocysteinuria
|
[NCBI]
|
3.56776e-05
|
|
|
niemann-pick disease, type c2
|
[NCBI]
|
3.56776e-05
|
|
|
hypotension, orthostatic
|
[NCBI]
|
3.56776e-05
|
|
|
FDH
|
[NCBI]
|
3.51035e-05
|
|
|
WFS1
|
[NCBI]
|
3.44806e-05
|
|
|
CHRNB2
|
[NCBI]
|
3.38766e-05
|
|
|
CCL25
|
[NCBI]
|
3.38766e-05
|
|
|
GAN
|
[NCBI]
|
3.38766e-05
|
|
|
SCA6
|
[NCBI]
|
3.38738e-05
|
|
|
APBD
|
[NCBI]
|
3.34599e-05
|
|
|
HDL2
|
[NCBI]
|
3.34599e-05
|
|
|
l-2-hydroxyglutaric aciduria
|
[NCBI]
|
3.34599e-05
|
|
|
WARBM
|
[NCBI]
|
3.34599e-05
|
|
|
pancreatic cancer, susceptibility to, 1
|
[NCBI]
|
3.34599e-05
|
|
|
MPD1
|
[NCBI]
|
3.34599e-05
|
|
|
FFI
|
[NCBI]
|
3.33468e-05
|
|
|
CDC25A
|
[NCBI]
|
3.22343e-05
|
|
|
SLN
|
[NCBI]
|
3.22343e-05
|
|
|
PIN1
|
[NCBI]
|
3.22343e-05
|
|
|
ZMPSTE24
|
[NCBI]
|
3.22343e-05
|
|
|
SYCP3
|
[NCBI]
|
3.22343e-05
|
|
|
PWS
|
[NCBI]
|
3.20654e-05
|
|
|
EGF
|
[NCBI]
|
3.16249e-05
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
3.15342e-05
|
|
|
TRS
|
[NCBI]
|
3.15342e-05
|
|
|
whistling face syndrome, recessive form
|
[NCBI]
|
3.15342e-05
|
|
|
peters-plus syndrome
|
[NCBI]
|
3.15342e-05
|
|
|
martsolf syndrome
|
[NCBI]
|
3.15342e-05
|
|
|
VLDLRCH
|
[NCBI]
|
3.15342e-05
|
|
|
JMJD6
|
[NCBI]
|
3.08316e-05
|
|
|
NPC2
|
[NCBI]
|
3.08316e-05
|
|
|
UBB
|
[NCBI]
|
3.08316e-05
|
|
|
DM2
|
[NCBI]
|
3.05335e-05
|
|
|
CHM
|
[NCBI]
|
3.00218e-05
|
|
|
MTTL1
|
[NCBI]
|
2.98422e-05
|
|
|
SCZD9
|
[NCBI]
|
2.98353e-05
|
|
|
AKT2
|
[NCBI]
|
2.96081e-05
|
|
|
FGF7
|
[NCBI]
|
2.86605e-05
|
|
|
CRB1
|
[NCBI]
|
2.85235e-05
|
|
|
de sanctis-cacchione syndrome
|
[NCBI]
|
2.83176e-05
|
|
|
amyloidosis vii
|
[NCBI]
|
2.83176e-05
|
|
|
spinocerebellar ataxia, 16q22-linked
|
[NCBI]
|
2.83176e-05
|
|
|
KLRK1
|
[NCBI]
|
2.75501e-05
|
|
|
SCN8A
|
[NCBI]
|
2.75501e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
2.71796e-05
|
|
|
kindler syndrome
|
[NCBI]
|
2.69478e-05
|
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
[NCBI]
|
2.69478e-05
|
|
|
PG
|
[NCBI]
|
2.6947e-05
|
|
|
CFH
|
[NCBI]
|
2.63891e-05
|
|
|
CACNA1F
|
[NCBI]
|
2.58604e-05
|
|
|
E2F1
|
[NCBI]
|
2.58604e-05
|
|
|
ACCPN
|
[NCBI]
|
2.57014e-05
|
|
|
MERRF
|
[NCBI]
|
2.57014e-05
|
|
|
renal cysts and diabetes syndrome
|
[NCBI]
|
2.57014e-05
|
|
|
NGFB
|
[NCBI]
|
2.53029e-05
|
|
|
indifference to pain, congenital, autosomal recessive
|
[NCBI]
|
2.45592e-05
|
|
|
alsin
|
[NCBI]
|
2.44289e-05
|
|
|
TIMP1
|
[NCBI]
|
2.44289e-05
|
|
|
ATXN3
|
[NCBI]
|
2.44289e-05
|
|
|
ABP1
|
[NCBI]
|
2.37093e-05
|
|
|
FA
|
[NCBI]
|
2.35691e-05
|
|
|
CDS
|
[NCBI]
|
2.35063e-05
|
|
|
WGN1
|
[NCBI]
|
2.35063e-05
|
|
|
ALS2
|
[NCBI]
|
2.35063e-05
|
|
|
DSMA1
|
[NCBI]
|
2.35063e-05
|
|
|
KL
|
[NCBI]
|
2.31885e-05
|
|
|
DISC1
|
[NCBI]
|
2.31885e-05
|
|
|
SPG7
|
[NCBI]
|
2.26257e-05
|
|
|
coenzyme q10 deficiency
|
[NCBI]
|
2.25308e-05
|
|
|
COFS1
|
[NCBI]
|
2.25308e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.24642e-05
|
|
|
MAP2
|
[NCBI]
|
2.19695e-05
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
2.1623e-05
|
|
|
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
[NCBI]
|
2.1623e-05
|
|
|
TTN
|
[NCBI]
|
2.15943e-05
|
|
|
GDNF
|
[NCBI]
|
2.11595e-05
|
|
|
3-@hydroxy-3-methylglutaryl-coa lyase deficiency
|
[NCBI]
|
2.11194e-05
|
|
|
RBP4
|
[NCBI]
|
2.11194e-05
|
|
|
PYGM
|
[NCBI]
|
2.11194e-05
|
|
|
EIG
|
[NCBI]
|
2.08889e-05
|
|
|
carbamoyl phosphate synthetase i deficiency, hyperammonemia due to
|
[NCBI]
|
2.07749e-05
|
|
|
INAD1
|
[NCBI]
|
2.07749e-05
|
|
|
CORD2
|
[NCBI]
|
2.07749e-05
|
|
|
LPI
|
[NCBI]
|
2.07702e-05
|
|
|
AGTR1
|
[NCBI]
|
2.06681e-05
|
|
|
XK
|
[NCBI]
|
2.06681e-05
|
|
|
FTL
|
[NCBI]
|
2.02384e-05
|
|
|
HNF1B
|
[NCBI]
|
2.02384e-05
|
|
|
TBP
|
[NCBI]
|
2.02384e-05
|
|
|
APTX
|
[NCBI]
|
2.02384e-05
|
|
|
VED
|
[NCBI]
|
1.99799e-05
|
|
|
KFSD
|
[NCBI]
|
1.99799e-05
|
|
|
CCL21
|
[NCBI]
|
1.98284e-05
|
|
|
AKT1
|
[NCBI]
|
1.87007e-05
|
|
|
RTD
|
[NCBI]
|
1.85274e-05
|
|
|
FGF1
|
[NCBI]
|
1.83548e-05
|
|
|
MICA
|
[NCBI]
|
1.83548e-05
|
|
|
EGFR
|
[NCBI]
|
1.80988e-05
|
|
|
ARX
|
[NCBI]
|
1.8022e-05
|
|
|
SCD
|
[NCBI]
|
1.8022e-05
|
|
|
EPS
|
[NCBI]
|
1.78612e-05
|
|
|
menkes disease
|
[NCBI]
|
1.78214e-05
|
|
|
ATF3
|
[NCBI]
|
1.73923e-05
|
|
|
GRN
|
[NCBI]
|
1.73923e-05
|
|
|
GSD
|
[NCBI]
|
1.72302e-05
|
|
|
PBD
|
[NCBI]
|
1.72302e-05
|
|
|
PDE6B
|
[NCBI]
|
1.70938e-05
|
|
|
pancreatic carcinoma
|
[NCBI]
|
1.66311e-05
|
|
|
DRD2
|
[NCBI]
|
1.62563e-05
|
|
|
TNFRSF6
|
[NCBI]
|
1.62563e-05
|
|
|
TNF
|
[NCBI]
|
1.60728e-05
|
|
|
GAN1
|
[NCBI]
|
1.60615e-05
|
|
|
cutis laxa, x-linked
|
[NCBI]
|
1.60615e-05
|
|
|
EA2
|
[NCBI]
|
1.60615e-05
|
|
|
NDP
|
[NCBI]
|
1.59946e-05
|
|
|
FRAP1
|
[NCBI]
|
1.56685e-05
|
|
|
AVP
|
[NCBI]
|
1.56682e-05
|
|
|
PSNP1
|
[NCBI]
|
1.55189e-05
|
|
|
MADA
|
[NCBI]
|
1.55189e-05
|
|
|
VWM
|
[NCBI]
|
1.55189e-05
|
|
|
AEZ
|
[NCBI]
|
1.55189e-05
|
|
|
temporal arteritis
|
[NCBI]
|
1.51296e-05
|
|
|
MELAS
|
[NCBI]
|
1.50013e-05
|
|
|
POF1
|
[NCBI]
|
1.50013e-05
|
|
|
FSHMD1A
|
[NCBI]
|
1.49809e-05
|
|
|
ETM1
|
[NCBI]
|
1.45068e-05
|
|
|
GFAP
|
[NCBI]
|
1.41178e-05
|
|
|
HMI
|
[NCBI]
|
1.37503e-05
|
|
|
NPHP1
|
[NCBI]
|
1.35807e-05
|
|
|
CACNA1A
|
[NCBI]
|
1.31824e-05
|
|
|
AMACR
|
[NCBI]
|
1.31824e-05
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
1.31463e-05
|
|
|
MBP
|
[NCBI]
|
1.28848e-05
|
|
|
mucolipidosis iv
|
[NCBI]
|
1.27293e-05
|
|
|
MYH7
|
[NCBI]
|
1.26526e-05
|
|
|
GPT
|
[NCBI]
|
1.23185e-05
|
|
|
MPO
|
[NCBI]
|
1.22449e-05
|
|
|
HGF
|
[NCBI]
|
1.20139e-05
|
|
|
FPLD2
|
[NCBI]
|
1.19434e-05
|
|
|
B2M
|
[NCBI]
|
1.1843e-05
|
|
|
KLK3
|
[NCBI]
|
1.17233e-05
|
|
|
FRDA
|
[NCBI]
|
1.12971e-05
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
1.12154e-05
|
|
|
usher syndrome, type i
|
[NCBI]
|
1.12154e-05
|
|
|
glycogen storage disease v
|
[NCBI]
|
1.12154e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
1.08711e-05
|
|
|
IL10
|
[NCBI]
|
1.07049e-05
|
|
|
CCK
|
[NCBI]
|
1.02773e-05
|
|
|
DFSP
|
[NCBI]
|
8.95691e-06
|
|
|
VMD
|
[NCBI]
|
8.50666e-06
|
|
|
SLC6A4
|
[NCBI]
|
8.27804e-06
|
|
|
NEM3
|
[NCBI]
|
8.00605e-06
|
|
|
melanoma, uveal
|
[NCBI]
|
7.76717e-06
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
7.53547e-06
|
|
|
CDG1A
|
[NCBI]
|
7.53547e-06
|
|
|
TNFSF6
|
[NCBI]
|
7.33114e-06
|
|
|
ADHD
|
[NCBI]
|
7.31067e-06
|
|
|
CNTF
|
[NCBI]
|
7.15503e-06
|
|
|
CVID
|
[NCBI]
|
7.07872e-06
|
|
|
GNRH1
|
[NCBI]
|
6.89608e-06
|
|
|
CDK2
|
[NCBI]
|
6.80021e-06
|
|
|
CSA
|
[NCBI]
|
6.67496e-06
|
|
|
CHAT
|
[NCBI]
|
6.66141e-06
|
|
|
CTNS
|
[NCBI]
|
6.47514e-06
|
|
|
TH
|
[NCBI]
|
6.45027e-06
|
|
|
CTGF
|
[NCBI]
|
6.4033e-06
|
|
|
KSS
|
[NCBI]
|
6.3487e-06
|
|
|
CDK4
|
[NCBI]
|
6.24534e-06
|
|
|
SST
|
[NCBI]
|
5.80141e-06
|
|
|
AFP
|
[NCBI]
|
5.72586e-06
|
|
|
MB
|
[NCBI]
|
5.68103e-06
|
|
|
TF
|
[NCBI]
|
5.63012e-06
|
|
|
amyloidosis vi
|
[NCBI]
|
5.53738e-06
|
|
|
HMBS
|
[NCBI]
|
5.50547e-06
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
5.22422e-06
|
|
|
RP
|
[NCBI]
|
4.36256e-06
|
|
|
LNS
|
[NCBI]
|
4.32775e-06
|
|
|
AR
|
[NCBI]
|
4.21569e-06
|
|
|
ND
|
[NCBI]
|
4.19186e-06
|
|
|
AMC
|
[NCBI]
|
4.05953e-06
|
|
|
PEDF
|
[NCBI]
|
4.0286e-06
|
|
|
SPINK1
|
[NCBI]
|
3.98678e-06
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
3.93066e-06
|
|
|
ADM
|
[NCBI]
|
3.86375e-06
|
|
|
OSM
|
[NCBI]
|
3.62826e-06
|
|
|
IAPP
|
[NCBI]
|
3.3347e-06
|
|
|
HGPS
|
[NCBI]
|
3.22478e-06
|
|
|
FMR1
|
[NCBI]
|
2.96564e-06
|
|
|
NPPA
|
[NCBI]
|
2.88883e-06
|
|
|
PRL
|
[NCBI]
|
2.7937e-06
|
|
|
MG
|
[NCBI]
|
2.70261e-06
|
|
|
ALS1
|
[NCBI]
|
2.62165e-06
|
|
|
CHS
|
[NCBI]
|
2.53997e-06
|
|
|
CYP1A1
|
[NCBI]
|
2.49165e-06
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
2.44082e-06
|
|
|
PRNP
|
[NCBI]
|
2.43712e-06
|
|
|
TYMS
|
[NCBI]
|
2.31267e-06
|
|
|
VDR
|
[NCBI]
|
1.98171e-06
|
|
|
STAT3
|
[NCBI]
|
1.94277e-06
|
|
|
GHRH
|
[NCBI]
|
1.92031e-06
|
|
|
TTR
|
[NCBI]
|
1.5906e-06
|
|
|
VIP
|
[NCBI]
|
1.56487e-06
|
|
|
PXE
|
[NCBI]
|
1.5531e-06
|
|
|
SOD1
|
[NCBI]
|
1.49252e-06
|
|
|
LPL
|
[NCBI]
|
9.72514e-07
|
|
|
MDD
|
[NCBI]
|
9.34648e-07
|
|
|
wilson disease
|
[NCBI]
|
7.63993e-07
|
|
|
CAT
|
[NCBI]
|
7.11757e-07
|
|
|
SHBG
|
[NCBI]
|
6.27191e-07
|
|
|
WBS
|
[NCBI]
|
6.11787e-07
|
|
|
RTT
|
[NCBI]
|
6.09261e-07
|
|
|
SLC6A3
|
[NCBI]
|
4.80516e-07
|
|
|
TSD
|
[NCBI]
|
4.71982e-07
|
|
|
SHH
|
[NCBI]
|
4.1412e-07
|
|
|
GAPDH
|
[NCBI]
|
4.1412e-07
|
|
|
leber optic atrophy
|
[NCBI]
|
3.28916e-07
|
|
|
TLR4
|
[NCBI]
|
2.32063e-07
|
|
|
ACPP
|
[NCBI]
|
1.47529e-07
|
|
|
OPMD
|
[NCBI]
|
1.39953e-07
|
|
|
CRH
|
[NCBI]
|
9.78435e-08
|
|
|
ACP5
|
[NCBI]
|
9.35911e-08
|
|
|
AS
|
[NCBI]
|
9.2769e-08
|
|
|
AT
|
[NCBI]
|
9.2769e-08
|
|
|
ACHE
|
[NCBI]
|
2.04267e-08
|
|