|
OMIM |
Link |
Information gain |
01 |
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.003485038
|
|
|
CORD1
|
[NCBI]
|
0.003035821
|
|
|
dermatoglyphics--fingerprint pattern
|
[NCBI]
|
0.003035821
|
|
|
noonan syndrome 2
|
[NCBI]
|
0.00287142
|
|
|
cataract, central saccular, with sutural opacities
|
[NCBI]
|
0.002414172
|
|
|
RIEG2
|
[NCBI]
|
0.00234952
|
|
|
CTAA1
|
[NCBI]
|
0.002301536
|
|
|
cataract, autosomal recessive, early-onset, pulverulent
|
[NCBI]
|
0.002218052
|
|
|
CTPP1
|
[NCBI]
|
0.002105416
|
|
|
CTAA2
|
[NCBI]
|
0.00202652
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.00202652
|
|
|
MCDU
|
[NCBI]
|
0.00185791
|
|
|
CCA1
|
[NCBI]
|
0.00184638
|
|
|
OTSC1
|
[NCBI]
|
0.001724259
|
|
|
pygmy
|
[NCBI]
|
0.001448543
|
|
|
glaucoma-related pigment dispersion syndrome
|
[NCBI]
|
0.001428822
|
|
|
holoprosencephaly
|
[NCBI]
|
0.001350424
|
|
|
hemophagocytic lymphohistiocytosis, familial, 1
|
[NCBI]
|
0.001020563
|
|
|
OFC1
|
[NCBI]
|
0.000744356
|
|
|
RENT1
|
[NCBI]
|
0.000463722
|
|
|
three m syndrome
|
[NCBI]
|
0.000373228
|
|
|
WAS
|
[NCBI]
|
0.000345457
|
|
|
RTT
|
[NCBI]
|
0.000309272
|
|
|
BCNS
|
[NCBI]
|
0.000308994
|
|
|
CCM3
|
[NCBI]
|
0.000286666
|
|
|
SYNS1
|
[NCBI]
|
0.000275237
|
|
|
CF
|
[NCBI]
|
0.000274107
|
|
|
PXE
|
[NCBI]
|
0.000258324
|
|
|
MCPH5
|
[NCBI]
|
0.000255333
|
|
|
BCPM
|
[NCBI]
|
0.000253457
|
|
|
SMEI
|
[NCBI]
|
0.000245503
|
|
|
CMT4A
|
[NCBI]
|
0.00024144
|
|
|
NETH
|
[NCBI]
|
0.000231249
|
|
|
ASD4
|
[NCBI]
|
0.000228274
|
|
|
ciliary dyskinesia, primary, 6
|
[NCBI]
|
0.000228274
|
|
|
RCD4
|
[NCBI]
|
0.000228274
|
|
|
RCD3B
|
[NCBI]
|
0.000228274
|
|
|
ARB
|
[NCBI]
|
0.000228274
|
|
|
oligodontia-colorectal cancer syndrome
|
[NCBI]
|
0.000228274
|
|
|
aphakia, congenital primary
|
[NCBI]
|
0.000228274
|
|
|
skin fragility-woolly hair syndrome
|
[NCBI]
|
0.000228274
|
|
|
APC
|
[NCBI]
|
0.0002273711
|
|
|
EVR1
|
[NCBI]
|
0.0002268486
|
|
|
UMS
|
[NCBI]
|
0.0002220474
|
|
|
HOS
|
[NCBI]
|
0.0002185451
|
|
|
ichthyosis congenita, harlequin fetus type
|
[NCBI]
|
0.0002178074
|
|
|
EV
|
[NCBI]
|
0.0002014781
|
|
|
filaminopathy, autosomal dominant
|
[NCBI]
|
0.0002005906
|
|
|
MRXS14
|
[NCBI]
|
0.0002005906
|
|
|
hyperlipoproteinemia, type v
|
[NCBI]
|
0.0001968002
|
|
|
FBS
|
[NCBI]
|
0.0001911123
|
|
|
stapes ankylosis with broad thumb and toes
|
[NCBI]
|
0.0001901981
|
|
|
OODD
|
[NCBI]
|
0.0001901981
|
|
|
SCA11
|
[NCBI]
|
0.0001901981
|
|
|
CCD
|
[NCBI]
|
0.000189603
|
|
|
UPF2
|
[NCBI]
|
0.0001877824
|
|
|
EGF
|
[NCBI]
|
0.0001844939
|
|
|
UPF3B
|
[NCBI]
|
0.0001811561
|
|
|
MFS
|
[NCBI]
|
0.0001763445
|
|
|
hyperekplexia, hereditary
|
[NCBI]
|
0.0001730753
|
|
|
CDG2H
|
[NCBI]
|
0.0001691168
|
|
|
autism, x-linked, susceptibility to, 3
|
[NCBI]
|
0.0001691168
|
|
|
MCOP3
|
[NCBI]
|
0.0001691168
|
|
|
amish infantile epilepsy syndrome
|
[NCBI]
|
0.0001691168
|
|
|
deafness, autosomal dominant nonsyndromic sensorineural, due to mutation in myo1a
|
[NCBI]
|
0.0001691168
|
|
|
ehlers-danlos syndrome, autosomal recessive, cardiac valvular form
|
[NCBI]
|
0.0001691168
|
|
|
ECM1
|
[NCBI]
|
0.0001672251
|
|
|
STGD1
|
[NCBI]
|
0.0001629256
|
|
|
glycogen storage disease iii
|
[NCBI]
|
0.0001628968
|
|
|
ARVD11
|
[NCBI]
|
0.0001587243
|
|
|
methylmalonyl-coa epimerase deficiency
|
[NCBI]
|
0.0001573102
|
|
|
SLC22A5
|
[NCBI]
|
0.0001541915
|
|
|
MRT2
|
[NCBI]
|
0.0001520072
|
|
|
hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration
|
[NCBI]
|
0.0001496841
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
0.0001477067
|
|
|
hypospadias, x-linked
|
[NCBI]
|
0.0001469177
|
|
|
ehlers-danlos-like syndrome due to tenascin-x deficiency
|
[NCBI]
|
0.0001469177
|
|
|
FEB4
|
[NCBI]
|
0.0001469177
|
|
|
MECP2
|
[NCBI]
|
0.0001439315
|
|
|
GLC1A
|
[NCBI]
|
0.0001434126
|
|
|
ATS
|
[NCBI]
|
0.0001428165
|
|
|
ABCC6
|
[NCBI]
|
0.0001410604
|
|
|
LCA5
|
[NCBI]
|
0.0001402006
|
|
|
papilloma of choroid plexus
|
[NCBI]
|
0.0001402006
|
|
|
charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive
|
[NCBI]
|
0.0001402006
|
|
|
DPR
|
[NCBI]
|
0.0001402006
|
|
|
hypotrichosis simplex of scalp
|
[NCBI]
|
0.0001398281
|
|
|
MRX59
|
[NCBI]
|
0.0001352291
|
|
|
LCA2
|
[NCBI]
|
0.0001352291
|
|
|
witkop syndrome
|
[NCBI]
|
0.0001352291
|
|
|
BPES
|
[NCBI]
|
0.0001343932
|
|
|
LGMD2K
|
[NCBI]
|
0.0001325745
|
|
|
FHL4
|
[NCBI]
|
0.0001325745
|
|
|
lipase deficiency, combined
|
[NCBI]
|
0.0001325745
|
|
|
DJS
|
[NCBI]
|
0.0001319596
|
|
|
goldberg-shprintzen megacolon syndrome
|
[NCBI]
|
0.0001312856
|
|
|
polydactyly, preaxial iv
|
[NCBI]
|
0.0001312856
|
|
|
RP
|
[NCBI]
|
0.0001292834
|
|
|
RCD3A
|
[NCBI]
|
0.000127603
|
|
|
CCZS
|
[NCBI]
|
0.000127603
|
|
|
CTPP3
|
[NCBI]
|
0.000127603
|
|
|
DFNA10
|
[NCBI]
|
0.000127603
|
|
|
OPTB5
|
[NCBI]
|
0.000127603
|
|
|
VWS
|
[NCBI]
|
0.0001273115
|
|
|
CDG1D
|
[NCBI]
|
0.0001269339
|
|
|
MLASA
|
[NCBI]
|
0.0001269339
|
|
|
insulin-like growth factor i, resistance to
|
[NCBI]
|
0.0001254813
|
|
|
FBN1
|
[NCBI]
|
0.0001247857
|
|
|
DFNB7
|
[NCBI]
|
0.0001236595
|
|
|
keratosis palmoplantaris striata i
|
[NCBI]
|
0.0001219624
|
|
|
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance
|
[NCBI]
|
0.0001219624
|
|
|
glycogen storage disease 0, muscle
|
[NCBI]
|
0.0001219624
|
|
|
UPF3A
|
[NCBI]
|
0.0001205369
|
|
|
ARL11
|
[NCBI]
|
0.0001205369
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
0.0001203954
|
|
|
naegeli syndrome
|
[NCBI]
|
0.0001203954
|
|
|
pierson syndrome
|
[NCBI]
|
0.0001203954
|
|
|
AN2
|
[NCBI]
|
0.0001195727
|
|
|
homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cble complementation type
|
[NCBI]
|
0.0001187642
|
|
|
CCM
|
[NCBI]
|
0.0001184406
|
|
|
CCM2
|
[NCBI]
|
0.0001180189
|
|
|
elejalde disease
|
[NCBI]
|
0.0001180189
|
|
|
opitz syndrome
|
[NCBI]
|
0.0001176142
|
|
|
niemann-pick disease, type c2
|
[NCBI]
|
0.0001174912
|
|
|
renal tubular acidosis, proximal, with ocular abnormalities and mental retardation
|
[NCBI]
|
0.0001174912
|
|
|
SLC6A8
|
[NCBI]
|
0.000117139
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
0.0001157182
|
|
|
CLPED1
|
[NCBI]
|
0.0001151939
|
|
|
CRC
|
[NCBI]
|
0.00011365
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative
|
[NCBI]
|
0.0001135477
|
|
|
cataract, lamellar
|
[NCBI]
|
0.0001135477
|
|
|
choreoathetosis, hypothyroidism, and neonatal respiratory distress
|
[NCBI]
|
0.0001135477
|
|
|
FPLD3
|
[NCBI]
|
0.0001135477
|
|
|
AIH2
|
[NCBI]
|
0.0001119736
|
|
|
HNF1B
|
[NCBI]
|
0.0001106452
|
|
|
enterokinase deficiency
|
[NCBI]
|
0.0001106434
|
|
|
HAE
|
[NCBI]
|
0.0001103512
|
|
|
CCA2
|
[NCBI]
|
0.0001102836
|
|
|
PAX6
|
[NCBI]
|
0.0001098083
|
|
|
prostate cancer/brain cancer susceptibility
|
[NCBI]
|
0.0001075024
|
|
|
NEM2
|
[NCBI]
|
0.0001065851
|
|
|
FMO2
|
[NCBI]
|
0.0001065851
|
|
|
CZP3
|
[NCBI]
|
0.0001065851
|
|
|
marshall syndrome
|
[NCBI]
|
0.0001054971
|
|
|
TCOF
|
[NCBI]
|
0.0001054172
|
|
|
CMT4B2
|
[NCBI]
|
0.0001050821
|
|
|
SYM1
|
[NCBI]
|
0.0001050821
|
|
|
CUL7
|
[NCBI]
|
0.0001041254
|
|
|
citrullinemia, type ii, neonatal-onset
|
[NCBI]
|
0.0001038039
|
|
|
HPS2
|
[NCBI]
|
0.0001038039
|
|
|
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus
|
[NCBI]
|
0.0001038039
|
|
|
creatine deficiency syndrome, x-linked
|
[NCBI]
|
0.0001006546
|
|
|
HPS
|
[NCBI]
|
0.0001003215
|
|
|
kindler syndrome
|
[NCBI]
|
9.92436e-05
|
|
|
SMG5
|
[NCBI]
|
9.9014e-05
|
|
|
SMG6
|
[NCBI]
|
9.9014e-05
|
|
|
SMG7
|
[NCBI]
|
9.9014e-05
|
|
|
methylcobalamin deficiency, cblg type
|
[NCBI]
|
9.82771e-05
|
|
|
hyperlipidemia, combined, 1
|
[NCBI]
|
9.82343e-05
|
|
|
CMH4
|
[NCBI]
|
9.82343e-05
|
|
|
indifference to pain, congenital, autosomal recessive
|
[NCBI]
|
9.77118e-05
|
|
|
HTX1
|
[NCBI]
|
9.73274e-05
|
|
|
MCOPS3
|
[NCBI]
|
9.73274e-05
|
|
|
ehlers-danlos syndrome, type ii
|
[NCBI]
|
9.73274e-05
|
|
|
CHST6
|
[NCBI]
|
9.70485e-05
|
|
|
complement factor i deficiency
|
[NCBI]
|
9.54956e-05
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
|
[NCBI]
|
9.54956e-05
|
|
|
HFE3
|
[NCBI]
|
9.54956e-05
|
|
|
ATP2C1
|
[NCBI]
|
9.4866e-05
|
|
|
DMD
|
[NCBI]
|
9.46335e-05
|
|
|
OSMED
|
[NCBI]
|
9.41781e-05
|
|
|
BDB1
|
[NCBI]
|
9.41781e-05
|
|
|
NR0B1
|
[NCBI]
|
9.34819e-05
|
|
|
PKD3
|
[NCBI]
|
9.33556e-05
|
|
|
proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis
|
[NCBI]
|
9.33306e-05
|
|
|
SPCH1
|
[NCBI]
|
9.25099e-05
|
|
|
GLA
|
[NCBI]
|
9.05973e-05
|
|
|
NDUFS4
|
[NCBI]
|
8.99445e-05
|
|
|
ACTN3
|
[NCBI]
|
8.9787e-05
|
|
|
PJS
|
[NCBI]
|
8.94309e-05
|
|
|
NFNS
|
[NCBI]
|
8.9412e-05
|
|
|
growth hormone insensitivity with immunodeficiency
|
[NCBI]
|
8.89531e-05
|
|
|
cystathioninuria
|
[NCBI]
|
8.79521e-05
|
|
|
renal cysts and diabetes syndrome
|
[NCBI]
|
8.72862e-05
|
|
|
encephalopathy, neonatal severe, due to mecp2 mutations
|
[NCBI]
|
8.72862e-05
|
|
|
NF1
|
[NCBI]
|
8.70194e-05
|
|
|
CORDX1
|
[NCBI]
|
8.66733e-05
|
|
|
ARVD1
|
[NCBI]
|
8.66733e-05
|
|
|
WAS
|
[NCBI]
|
8.58637e-05
|
|
|
MCDS
|
[NCBI]
|
8.57053e-05
|
|
|
NCIE1
|
[NCBI]
|
8.57053e-05
|
|
|
FZD4
|
[NCBI]
|
8.57034e-05
|
|
|
morquio syndrome b
|
[NCBI]
|
8.55318e-05
|
|
|
MCPH1
|
[NCBI]
|
8.53317e-05
|
|
|
RTD
|
[NCBI]
|
8.39604e-05
|
|
|
hypouricemia, renal
|
[NCBI]
|
8.33918e-05
|
|
|
CTLN2
|
[NCBI]
|
8.33918e-05
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
8.31637e-05
|
|
|
AIS
|
[NCBI]
|
8.29072e-05
|
|
|
ASPM
|
[NCBI]
|
8.22076e-05
|
|
|
CRYGC
|
[NCBI]
|
8.11812e-05
|
|
|
LGMD1B
|
[NCBI]
|
8.01308e-05
|
|
|
RPGR
|
[NCBI]
|
7.97422e-05
|
|
|
severe combined immunodeficiency with sensitivity to ionizing radiation
|
[NCBI]
|
7.95004e-05
|
|
|
GALNT3
|
[NCBI]
|
7.92419e-05
|
|
|
LGMD2B
|
[NCBI]
|
7.87892e-05
|
|
|
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities
|
[NCBI]
|
7.83469e-05
|
|
|
CORD2
|
[NCBI]
|
7.83381e-05
|
|
|
TRAPPC2
|
[NCBI]
|
7.82991e-05
|
|
|
pseudoxanthoma elasticum, forme fruste
|
[NCBI]
|
7.75432e-05
|
|
|
mowat-wilson syndrome
|
[NCBI]
|
7.70053e-05
|
|
|
MCDC1
|
[NCBI]
|
7.68276e-05
|
|
|
MCOLN1
|
[NCBI]
|
7.66637e-05
|
|
|
GDAP1
|
[NCBI]
|
7.66167e-05
|
|
|
PCLD
|
[NCBI]
|
7.62266e-05
|
|
|
PCSK9
|
[NCBI]
|
7.57919e-05
|
|
|
bartter syndrome, antenatal, type 2
|
[NCBI]
|
7.52467e-05
|
|
|
PRX
|
[NCBI]
|
7.50613e-05
|
|
|
PRDM1
|
[NCBI]
|
7.49813e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
7.47961e-05
|
|
|
RIEG1
|
[NCBI]
|
7.43508e-05
|
|
|
ENAM
|
[NCBI]
|
7.42507e-05
|
|
|
COL5A1
|
[NCBI]
|
7.34934e-05
|
|
|
deafness, conductive, with stapes fixation
|
[NCBI]
|
7.34871e-05
|
|
|
IRF6
|
[NCBI]
|
7.28107e-05
|
|
|
PARK6
|
[NCBI]
|
7.26101e-05
|
|
|
neuropathy, congenital hypomyelinating
|
[NCBI]
|
7.14478e-05
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
7.12629e-05
|
|
|
SCNM1
|
[NCBI]
|
7.10392e-05
|
|
|
NOM1
|
[NCBI]
|
7.10392e-05
|
|
|
BLOC1S2
|
[NCBI]
|
7.10392e-05
|
|
|
FGB
|
[NCBI]
|
7.0856e-05
|
|
|
GLRA1
|
[NCBI]
|
7.07902e-05
|
|
|
FTLDU
|
[NCBI]
|
7.03592e-05
|
|
|
SHEP2
|
[NCBI]
|
7.03592e-05
|
|
|
danon disease
|
[NCBI]
|
6.99213e-05
|
|
|
FOXC1
|
[NCBI]
|
6.96166e-05
|
|
|
NHS
|
[NCBI]
|
6.89723e-05
|
|
|
factor v deficiency
|
[NCBI]
|
6.89622e-05
|
|
|
CFTR
|
[NCBI]
|
6.84395e-05
|
|
|
HR
|
[NCBI]
|
6.83859e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
6.81086e-05
|
|
|
GEFS+
|
[NCBI]
|
6.79333e-05
|
|
|
C9
|
[NCBI]
|
6.73311e-05
|
|
|
usher syndrome, type i
|
[NCBI]
|
6.71419e-05
|
|
|
APS1
|
[NCBI]
|
6.70615e-05
|
|
|
EPHB2
|
[NCBI]
|
6.67618e-05
|
|
|
succinic semialdehyde dehydrogenase deficiency
|
[NCBI]
|
6.66668e-05
|
|
|
ESCS
|
[NCBI]
|
6.66254e-05
|
|
|
TMAU
|
[NCBI]
|
6.63637e-05
|
|
|
LAMB3
|
[NCBI]
|
6.62153e-05
|
|
|
canavan disease
|
[NCBI]
|
6.56611e-05
|
|
|
glucose transport defect, blood-brain barrier
|
[NCBI]
|
6.52751e-05
|
|
|
HFTC
|
[NCBI]
|
6.52475e-05
|
|
|
NR3C2
|
[NCBI]
|
6.52126e-05
|
|
|
NKX2-1
|
[NCBI]
|
6.47457e-05
|
|
|
epidermolysis bullosa letalis
|
[NCBI]
|
6.44372e-05
|
|
|
SDHD
|
[NCBI]
|
6.4299e-05
|
|
|
CRYAA
|
[NCBI]
|
6.42507e-05
|
|
|
BRCA1
|
[NCBI]
|
6.392e-05
|
|
|
donohue syndrome
|
[NCBI]
|
6.38859e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
6.38859e-05
|
|
|
propionic acidemia
|
[NCBI]
|
6.30735e-05
|
|
|
AIRE
|
[NCBI]
|
6.25759e-05
|
|
|
UCMD
|
[NCBI]
|
6.23764e-05
|
|
|
CRYAB
|
[NCBI]
|
6.15979e-05
|
|
|
APL
|
[NCBI]
|
6.12938e-05
|
|
|
NOG
|
[NCBI]
|
6.07705e-05
|
|
|
CGL2
|
[NCBI]
|
6.02712e-05
|
|
|
USH2A
|
[NCBI]
|
5.96097e-05
|
|
|
C1NH
|
[NCBI]
|
5.9275e-05
|
|
|
NEM3
|
[NCBI]
|
5.91673e-05
|
|
|
EGFR
|
[NCBI]
|
5.85872e-05
|
|
|
UOX
|
[NCBI]
|
5.84393e-05
|
|
|
refsum disease, infantile form
|
[NCBI]
|
5.84218e-05
|
|
|
pheochromocytoma
|
[NCBI]
|
5.73737e-05
|
|
|
SOX10
|
[NCBI]
|
5.7098e-05
|
|
|
giant platelet syndrome
|
[NCBI]
|
5.64776e-05
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
5.63511e-05
|
|
|
SPG4
|
[NCBI]
|
5.61137e-05
|
|
|
PTPN14
|
[NCBI]
|
5.53891e-05
|
|
|
RAX
|
[NCBI]
|
5.53891e-05
|
|
|
WNT10A
|
[NCBI]
|
5.53891e-05
|
|
|
KCNV2
|
[NCBI]
|
5.53891e-05
|
|
|
TBX20
|
[NCBI]
|
5.53891e-05
|
|
|
NDUFA12L
|
[NCBI]
|
5.53891e-05
|
|
|
SNAPAP
|
[NCBI]
|
5.53891e-05
|
|
|
BLOC1S3
|
[NCBI]
|
5.53891e-05
|
|
|
KIAA1279
|
[NCBI]
|
5.53891e-05
|
|
|
TXNDC3
|
[NCBI]
|
5.53891e-05
|
|
|
FMO3
|
[NCBI]
|
5.49257e-05
|
|
|
GDF5
|
[NCBI]
|
5.48862e-05
|
|
|
RPS6KA3
|
[NCBI]
|
5.45717e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
5.43972e-05
|
|
|
ehlers-danlos syndrome, type iv, autosomal dominant
|
[NCBI]
|
5.43012e-05
|
|
|
glycogen storage disease ib
|
[NCBI]
|
5.34186e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
5.32156e-05
|
|
|
PEPD
|
[NCBI]
|
5.31356e-05
|
|
|
MCEE
|
[NCBI]
|
5.25966e-05
|
|
|
MYO1A
|
[NCBI]
|
5.25966e-05
|
|
|
PPT1
|
[NCBI]
|
5.23328e-05
|
|
|
TTBK2
|
[NCBI]
|
5.22877e-05
|
|
|
LCA5
|
[NCBI]
|
5.22877e-05
|
|
|
DAR
|
[NCBI]
|
5.22586e-05
|
|
|
PKLR
|
[NCBI]
|
5.20841e-05
|
|
|
PBD
|
[NCBI]
|
5.1915e-05
|
|
|
RP3
|
[NCBI]
|
5.19071e-05
|
|
|
GRN
|
[NCBI]
|
5.18019e-05
|
|
|
methylmalonic aciduria due to methylmalonyl-coa mutase deficiency
|
[NCBI]
|
5.07054e-05
|
|
|
RSTS
|
[NCBI]
|
5.05471e-05
|
|
|
EVER1
|
[NCBI]
|
5.02778e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
5.01422e-05
|
|
|
TSC1
|
[NCBI]
|
4.9528e-05
|
|
|
PTPRT
|
[NCBI]
|
4.94952e-05
|
|
|
MPST
|
[NCBI]
|
4.94952e-05
|
|
|
TAAR9
|
[NCBI]
|
4.94952e-05
|
|
|
TAAR2
|
[NCBI]
|
4.94952e-05
|
|
|
MRPS22
|
[NCBI]
|
4.94952e-05
|
|
|
CACNA2D4
|
[NCBI]
|
4.94952e-05
|
|
|
OLFM3
|
[NCBI]
|
4.94952e-05
|
|
|
PDCD10
|
[NCBI]
|
4.94952e-05
|
|
|
CTH
|
[NCBI]
|
4.94952e-05
|
|
|
CRBN
|
[NCBI]
|
4.94952e-05
|
|
|
CYP2G1
|
[NCBI]
|
4.94952e-05
|
|
|
PGL1
|
[NCBI]
|
4.69785e-05
|
|
|
HSCR1
|
[NCBI]
|
4.69009e-05
|
|
|
TBS
|
[NCBI]
|
4.67226e-05
|
|
|
MSD
|
[NCBI]
|
4.63358e-05
|
|
|
SPG4
|
[NCBI]
|
4.57351e-05
|
|
|
hemophilia a
|
[NCBI]
|
4.5718e-05
|
|
|
SYNGR1
|
[NCBI]
|
4.56751e-05
|
|
|
CXORF6
|
[NCBI]
|
4.56751e-05
|
|
|
PTPN3
|
[NCBI]
|
4.56751e-05
|
|
|
LILRA3
|
[NCBI]
|
4.56751e-05
|
|
|
GPNMB
|
[NCBI]
|
4.56751e-05
|
|
|
AXIN2
|
[NCBI]
|
4.56751e-05
|
|
|
RPL12
|
[NCBI]
|
4.56751e-05
|
|
|
COG8
|
[NCBI]
|
4.56751e-05
|
|
|
cystinuria
|
[NCBI]
|
4.54219e-05
|
|
|
myoclonic dystonia
|
[NCBI]
|
4.50384e-05
|
|
|
sotos syndrome
|
[NCBI]
|
4.50304e-05
|
|
|
NF2
|
[NCBI]
|
4.49513e-05
|
|
|
citrullinemia, classic
|
[NCBI]
|
4.48108e-05
|
|
|
ALG3
|
[NCBI]
|
4.43315e-05
|
|
|
SLC25A15
|
[NCBI]
|
4.43315e-05
|
|
|
AP1S2
|
[NCBI]
|
4.41835e-05
|
|
|
FCHL
|
[NCBI]
|
4.41616e-05
|
|
|
CDH1
|
[NCBI]
|
4.40002e-05
|
|
|
CLL
|
[NCBI]
|
4.38711e-05
|
|
|
SLC2A2
|
[NCBI]
|
4.32192e-05
|
|
|
SBF2
|
[NCBI]
|
4.29973e-05
|
|
|
RB1
|
[NCBI]
|
4.29681e-05
|
|
|
PHF8
|
[NCBI]
|
4.28399e-05
|
|
|
PRSS7
|
[NCBI]
|
4.28399e-05
|
|
|
FOXE3
|
[NCBI]
|
4.28399e-05
|
|
|
ABCA12
|
[NCBI]
|
4.28399e-05
|
|
|
PUS1
|
[NCBI]
|
4.28399e-05
|
|
|
OSTM1
|
[NCBI]
|
4.28399e-05
|
|
|
NCBP1
|
[NCBI]
|
4.28399e-05
|
|
|
UBE2A
|
[NCBI]
|
4.28399e-05
|
|
|
WFS1
|
[NCBI]
|
4.27469e-05
|
|
|
MM
|
[NCBI]
|
4.20159e-05
|
|
|
LMF1
|
[NCBI]
|
4.17711e-05
|
|
|
C1S
|
[NCBI]
|
4.17711e-05
|
|
|
MLH3
|
[NCBI]
|
4.16537e-05
|
|
|
ALGS1
|
[NCBI]
|
4.10435e-05
|
|
|
NR5A1
|
[NCBI]
|
4.10176e-05
|
|
|
EPOR
|
[NCBI]
|
4.09594e-05
|
|
|
ST3GAL5
|
[NCBI]
|
4.05849e-05
|
|
|
DYNLL1
|
[NCBI]
|
4.05849e-05
|
|
|
GATM
|
[NCBI]
|
4.05849e-05
|
|
|
CRYBB3
|
[NCBI]
|
4.05849e-05
|
|
|
SLC22A12
|
[NCBI]
|
4.05849e-05
|
|
|
MAD1L1
|
[NCBI]
|
4.05849e-05
|
|
|
STX11
|
[NCBI]
|
4.05849e-05
|
|
|
BLOC1S1
|
[NCBI]
|
4.05849e-05
|
|
|
CST6
|
[NCBI]
|
3.96977e-05
|
|
|
NF2
|
[NCBI]
|
3.96817e-05
|
|
|
SCS
|
[NCBI]
|
3.96782e-05
|
|
|
NSDHL
|
[NCBI]
|
3.96003e-05
|
|
|
SATB2
|
[NCBI]
|
3.96003e-05
|
|
|
MC4R
|
[NCBI]
|
3.95445e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
3.88591e-05
|
|
|
MIRN15A
|
[NCBI]
|
3.87131e-05
|
|
|
VAMP1
|
[NCBI]
|
3.87131e-05
|
|
|
CRYBA4
|
[NCBI]
|
3.87131e-05
|
|
|
PTPN13
|
[NCBI]
|
3.87131e-05
|
|
|
CRYM
|
[NCBI]
|
3.87131e-05
|
|
|
VMD
|
[NCBI]
|
3.79897e-05
|
|
|
ABCC4
|
[NCBI]
|
3.7955e-05
|
|
|
ALDH5A1
|
[NCBI]
|
3.7955e-05
|
|
|
PRPF31
|
[NCBI]
|
3.78719e-05
|
|
|
LWD
|
[NCBI]
|
3.74684e-05
|
|
|
PTPRG
|
[NCBI]
|
3.71138e-05
|
|
|
PICALM
|
[NCBI]
|
3.71138e-05
|
|
|
FLNC
|
[NCBI]
|
3.71138e-05
|
|
|
DCLRE1C
|
[NCBI]
|
3.71138e-05
|
|
|
CRYBB1
|
[NCBI]
|
3.71138e-05
|
|
|
SLC25A13
|
[NCBI]
|
3.71138e-05
|
|
|
GNAT2
|
[NCBI]
|
3.71138e-05
|
|
|
TMC1
|
[NCBI]
|
3.71138e-05
|
|
|
GPR98
|
[NCBI]
|
3.63799e-05
|
|
|
MIRN16-1
|
[NCBI]
|
3.63799e-05
|
|
|
MTRR
|
[NCBI]
|
3.57182e-05
|
|
|
GRHPR
|
[NCBI]
|
3.57182e-05
|
|
|
OPHN1
|
[NCBI]
|
3.57182e-05
|
|
|
PDE11A
|
[NCBI]
|
3.57182e-05
|
|
|
DDB2
|
[NCBI]
|
3.57182e-05
|
|
|
SYNJ2
|
[NCBI]
|
3.57182e-05
|
|
|
CDG1A
|
[NCBI]
|
3.57155e-05
|
|
|
HOXA13
|
[NCBI]
|
3.51449e-05
|
|
|
hemojuvelin
|
[NCBI]
|
3.51314e-05
|
|
|
BSCL2
|
[NCBI]
|
3.51314e-05
|
|
|
CNGB3
|
[NCBI]
|
3.50674e-05
|
|
|
TNNI2
|
[NCBI]
|
3.50674e-05
|
|
|
MPZ
|
[NCBI]
|
3.47206e-05
|
|
|
CHS
|
[NCBI]
|
3.45384e-05
|
|
|
LI1
|
[NCBI]
|
3.44867e-05
|
|
|
TRPS1
|
[NCBI]
|
3.44806e-05
|
|
|
APOA5
|
[NCBI]
|
3.44806e-05
|
|
|
DSG4
|
[NCBI]
|
3.44806e-05
|
|
|
CDKL5
|
[NCBI]
|
3.44806e-05
|
|
|
DSC2
|
[NCBI]
|
3.41264e-05
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
3.40094e-05
|
|
|
hypophosphatemic rickets, x-linked dominant
|
[NCBI]
|
3.40044e-05
|
|
|
PTPRF
|
[NCBI]
|
3.39537e-05
|
|
|
SLC4A4
|
[NCBI]
|
3.39537e-05
|
|
|
ASS
|
[NCBI]
|
3.37521e-05
|
|
|
flaujeac factor deficiency
|
[NCBI]
|
3.34756e-05
|
|
|
GYS1
|
[NCBI]
|
3.33695e-05
|
|
|
SGKL
|
[NCBI]
|
3.33695e-05
|
|
|
PEX1
|
[NCBI]
|
3.33695e-05
|
|
|
TGIF
|
[NCBI]
|
3.33695e-05
|
|
|
ZIC3
|
[NCBI]
|
3.33664e-05
|
|
|
PITX3
|
[NCBI]
|
3.33664e-05
|
|
|
MCPH1
|
[NCBI]
|
3.28395e-05
|
|
|
EIF2AK3
|
[NCBI]
|
3.23614e-05
|
|
|
SCN8A
|
[NCBI]
|
3.23614e-05
|
|
|
BRIP1
|
[NCBI]
|
3.23614e-05
|
|
|
TBX3
|
[NCBI]
|
3.23614e-05
|
|
|
RPL3
|
[NCBI]
|
3.23614e-05
|
|
|
PAX9
|
[NCBI]
|
3.23614e-05
|
|
|
C10ORF2
|
[NCBI]
|
3.23614e-05
|
|
|
BFSP2
|
[NCBI]
|
3.23614e-05
|
|
|
FKTN
|
[NCBI]
|
3.23548e-05
|
|
|
SLC7A9
|
[NCBI]
|
3.19241e-05
|
|
|
DGUOK
|
[NCBI]
|
3.19241e-05
|
|
|
RAI1
|
[NCBI]
|
3.19084e-05
|
|
|
SIX3
|
[NCBI]
|
3.18767e-05
|
|
|
MID1
|
[NCBI]
|
3.18767e-05
|
|
|
NPC2
|
[NCBI]
|
3.14394e-05
|
|
|
RPGRIP1
|
[NCBI]
|
3.14394e-05
|
|
|
OCRL
|
[NCBI]
|
3.14394e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
3.12826e-05
|
|
|
CDSP
|
[NCBI]
|
3.10865e-05
|
|
|
XRN1
|
[NCBI]
|
3.10365e-05
|
|
|
LGI1
|
[NCBI]
|
3.10365e-05
|
|
|
SPINK5
|
[NCBI]
|
3.10365e-05
|
|
|
NCF2
|
[NCBI]
|
3.0993e-05
|
|
|
ART4
|
[NCBI]
|
3.06632e-05
|
|
|
alsin
|
[NCBI]
|
3.05901e-05
|
|
|
KCNJ1
|
[NCBI]
|
3.05901e-05
|
|
|
PVRL1
|
[NCBI]
|
3.05901e-05
|
|
|
hurler syndrome
|
[NCBI]
|
3.04341e-05
|
|
|
DMD
|
[NCBI]
|
3.02384e-05
|
|
|
CRYGD
|
[NCBI]
|
3.01765e-05
|
|
|
PKD1
|
[NCBI]
|
2.98383e-05
|
|
|
SALL1
|
[NCBI]
|
2.98032e-05
|
|
|
AP3B1
|
[NCBI]
|
2.97912e-05
|
|
|
FOXP2
|
[NCBI]
|
2.97912e-05
|
|
|
POMT1
|
[NCBI]
|
2.94179e-05
|
|
|
prekallikrein deficiency
|
[NCBI]
|
2.92378e-05
|
|
|
NSD1
|
[NCBI]
|
2.90923e-05
|
|
|
AGL
|
[NCBI]
|
2.90701e-05
|
|
|
SLC26A3
|
[NCBI]
|
2.90701e-05
|
|
|
MYBPC3
|
[NCBI]
|
2.90701e-05
|
|
|
CYBA
|
[NCBI]
|
2.90575e-05
|
|
|
ELAC2
|
[NCBI]
|
2.90575e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
2.90104e-05
|
|
|
CHM
|
[NCBI]
|
2.88066e-05
|
|
|
ROR2
|
[NCBI]
|
2.8719e-05
|
|
|
LYST
|
[NCBI]
|
2.87097e-05
|
|
|
BEST1
|
[NCBI]
|
2.87097e-05
|
|
|
ZEB2
|
[NCBI]
|
2.87097e-05
|
|
|
CRYBB2
|
[NCBI]
|
2.87097e-05
|
|
|
SCN9A
|
[NCBI]
|
2.83842e-05
|
|
|
NPHS1
|
[NCBI]
|
2.83842e-05
|
|
|
FLG
|
[NCBI]
|
2.83842e-05
|
|
|
SOX2
|
[NCBI]
|
2.83712e-05
|
|
|
CRYBA1
|
[NCBI]
|
2.83712e-05
|
|
|
SVAS
|
[NCBI]
|
2.83676e-05
|
|
|
PCCA
|
[NCBI]
|
2.82635e-05
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
2.82195e-05
|
|
|
MITF
|
[NCBI]
|
2.79884e-05
|
|
|
CRX
|
[NCBI]
|
2.774e-05
|
|
|
USH2A
|
[NCBI]
|
2.774e-05
|
|
|
C5
|
[NCBI]
|
2.77267e-05
|
|
|
TXNIP
|
[NCBI]
|
2.75178e-05
|
|
|
PANK2
|
[NCBI]
|
2.72594e-05
|
|
|
SLC16A2
|
[NCBI]
|
2.71793e-05
|
|
|
TSIX
|
[NCBI]
|
2.71328e-05
|
|
|
USH1C
|
[NCBI]
|
2.71328e-05
|
|
|
MAN2B1
|
[NCBI]
|
2.69209e-05
|
|
|
TGFBR1
|
[NCBI]
|
2.68603e-05
|
|
|
ITGB4
|
[NCBI]
|
2.68603e-05
|
|
|
INSR
|
[NCBI]
|
2.67282e-05
|
|
|
RDT
|
[NCBI]
|
2.67244e-05
|
|
|
HBA2
|
[NCBI]
|
2.65207e-05
|
|
|
ALD
|
[NCBI]
|
2.63501e-05
|
|
|
FOXL2
|
[NCBI]
|
2.60546e-05
|
|
|
NEB
|
[NCBI]
|
2.60143e-05
|
|
|
NEU1
|
[NCBI]
|
2.60143e-05
|
|
|
DHCR7
|
[NCBI]
|
2.57686e-05
|
|
|
SLC2A1
|
[NCBI]
|
2.57426e-05
|
|
|
SPR
|
[NCBI]
|
2.55971e-05
|
|
|
tay-sachs disease, ab variant
|
[NCBI]
|
2.55346e-05
|
|
|
CLCN5
|
[NCBI]
|
2.54969e-05
|
|
|
PYGM
|
[NCBI]
|
2.54969e-05
|
|
|
GATA4
|
[NCBI]
|
2.5238e-05
|
|
|
ND
|
[NCBI]
|
2.51774e-05
|
|
|
DSP
|
[NCBI]
|
2.50394e-05
|
|
|
ATP2A2
|
[NCBI]
|
2.47805e-05
|
|
|
WFS1
|
[NCBI]
|
2.47569e-05
|
|
|
CDSN
|
[NCBI]
|
2.47546e-05
|
|
|
MSX1
|
[NCBI]
|
2.47546e-05
|
|
|
GATA3
|
[NCBI]
|
2.45334e-05
|
|
|
ADAMTS13
|
[NCBI]
|
2.4362e-05
|
|
|
CHM
|
[NCBI]
|
2.4348e-05
|
|
|
APTX
|
[NCBI]
|
2.43197e-05
|
|
|
PINK1
|
[NCBI]
|
2.42971e-05
|
|
|
HMBS
|
[NCBI]
|
2.41301e-05
|
|
|
pta deficiency
|
[NCBI]
|
2.40771e-05
|
|
|
RPS19
|
[NCBI]
|
2.40708e-05
|
|
|
LRP5
|
[NCBI]
|
2.38571e-05
|
|
|
SLC3A1
|
[NCBI]
|
2.36523e-05
|
|
|
SCN1A
|
[NCBI]
|
2.36399e-05
|
|
|
MIP
|
[NCBI]
|
2.34557e-05
|
|
|
NPC1
|
[NCBI]
|
2.32873e-05
|
|
|
MTND2
|
[NCBI]
|
2.32385e-05
|
|
|
GALC
|
[NCBI]
|
2.32385e-05
|
|
|
OPA1
|
[NCBI]
|
2.32263e-05
|
|
|
XPC
|
[NCBI]
|
2.30638e-05
|
|
|
PAX2
|
[NCBI]
|
2.30496e-05
|
|
|
ELA2
|
[NCBI]
|
2.28678e-05
|
|
|
CTSK
|
[NCBI]
|
2.28408e-05
|
|
|
GJA8
|
[NCBI]
|
2.28289e-05
|
|
|
CHRNE
|
[NCBI]
|
2.24582e-05
|
|
|
MUT
|
[NCBI]
|
2.24582e-05
|
|
|
KRT14
|
[NCBI]
|
2.24464e-05
|
|
|
PROP1
|
[NCBI]
|
2.22829e-05
|
|
|
SLC25A4
|
[NCBI]
|
2.19202e-05
|
|
|
RS1
|
[NCBI]
|
2.185379e-05
|
|
|
GLI3
|
[NCBI]
|
2.17234e-05
|
|
|
COL4A5
|
[NCBI]
|
2.15533e-05
|
|
|
TWIST1
|
[NCBI]
|
2.139e-05
|
|
|
TGFBR2
|
[NCBI]
|
2.139e-05
|
|
|
DYSF
|
[NCBI]
|
2.13794e-05
|
|
|
GCH1
|
[NCBI]
|
2.12157e-05
|
|
|
CYP11B2
|
[NCBI]
|
2.093119e-05
|
|
|
FTL
|
[NCBI]
|
2.0905e-05
|
|
|
COL10A1
|
[NCBI]
|
2.07363e-05
|
|
|
IGF1R
|
[NCBI]
|
2.061333e-05
|
|
|
PAFAH1B1
|
[NCBI]
|
2.0573e-05
|
|
|
AK1
|
[NCBI]
|
2.047401e-05
|
|
|
MAOB
|
[NCBI]
|
2.044463e-05
|
|
|
CFI
|
[NCBI]
|
2.042489e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
2.033871e-05
|
|
|
POU1F1
|
[NCBI]
|
2.014201e-05
|
|
|
MYO7A
|
[NCBI]
|
1.982023e-05
|
|
|
MTCO2
|
[NCBI]
|
1.969471e-05
|
|
|
GATA1
|
[NCBI]
|
1.954561e-05
|
|
|
FANCA
|
[NCBI]
|
1.9536e-05
|
|
|
SHOX
|
[NCBI]
|
1.953442e-05
|
|
|
GLB1
|
[NCBI]
|
1.946462e-05
|
|
|
JAK1
|
[NCBI]
|
1.94007e-05
|
|
|
TS
|
[NCBI]
|
1.916617e-05
|
|
|
PDE6B
|
[NCBI]
|
1.912832e-05
|
|
|
JAG1
|
[NCBI]
|
1.900045e-05
|
|
|
ASPA
|
[NCBI]
|
1.889574e-05
|
|
|
STK11
|
[NCBI]
|
1.885778e-05
|
|
|
TPI1
|
[NCBI]
|
1.875484e-05
|
|
|
ATP7B
|
[NCBI]
|
1.84843e-05
|
|
|
glycogen storage disease i
|
[NCBI]
|
1.844077e-05
|
|
|
RP2
|
[NCBI]
|
1.823966e-05
|
|
|
SOX9
|
[NCBI]
|
1.810466e-05
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
1.803555e-05
|
|
|
TFR2
|
[NCBI]
|
1.799445e-05
|
|
|
ABCA4
|
[NCBI]
|
1.777263e-05
|
|
|
GAMT
|
[NCBI]
|
1.76517e-05
|
|
|
KCNH2
|
[NCBI]
|
1.755667e-05
|
|
|
SCP2
|
[NCBI]
|
1.748591e-05
|
|
|
POLG
|
[NCBI]
|
1.742155e-05
|
|
|
HEXB
|
[NCBI]
|
1.723565e-05
|
|
|
ZNF145
|
[NCBI]
|
1.719938e-05
|
|
|
RELN
|
[NCBI]
|
1.708445e-05
|
|
|
factor vii deficiency
|
[NCBI]
|
1.686155e-05
|
|
|
CTSC
|
[NCBI]
|
1.677021e-05
|
|
|
MSTN
|
[NCBI]
|
1.645546e-05
|
|
|
COL3A1
|
[NCBI]
|
1.645546e-05
|
|
|
CACNA1A
|
[NCBI]
|
1.625492e-05
|
|
|
ADHD
|
[NCBI]
|
1.619013e-05
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
1.605774e-05
|
|
|
SCN5A
|
[NCBI]
|
1.605157e-05
|
|
|
SMS
|
[NCBI]
|
1.589423e-05
|
|
|
MODY
|
[NCBI]
|
1.57487e-05
|
|
|
FGF23
|
[NCBI]
|
1.574359e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
1.557712e-05
|
|
|
LHCGR
|
[NCBI]
|
1.540761e-05
|
|
|
PROCR
|
[NCBI]
|
1.532311e-05
|
|
|
VHL
|
[NCBI]
|
1.530971e-05
|
|
|
KCNQ1
|
[NCBI]
|
1.522228e-05
|
|
|
OTC
|
[NCBI]
|
1.506434e-05
|
|
|
PKD2
|
[NCBI]
|
1.486876e-05
|
|
|
MMP9
|
[NCBI]
|
1.438312e-05
|
|
|
IGF1
|
[NCBI]
|
1.423334e-05
|
|
|
ELN
|
[NCBI]
|
1.405334e-05
|
|
|
LS
|
[NCBI]
|
1.38643e-05
|
|
|
GHR
|
[NCBI]
|
1.366495e-05
|
|
|
UGT1A1
|
[NCBI]
|
1.355257e-05
|
|
|
AHO
|
[NCBI]
|
1.342746e-05
|
|
|
JAK3
|
[NCBI]
|
1.327614e-05
|
|
|
TSC2
|
[NCBI]
|
1.323994e-05
|
|
|
CD36
|
[NCBI]
|
1.294923e-05
|
|
|
MLH1
|
[NCBI]
|
1.269172e-05
|
|
|
wilson disease
|
[NCBI]
|
1.216739e-05
|
|
|
TSHR
|
[NCBI]
|
1.176127e-05
|
|
|
IDUA
|
[NCBI]
|
1.164363e-05
|
|
|
VHL
|
[NCBI]
|
1.163865e-05
|
|
|
SLC11A2
|
[NCBI]
|
1.143759e-05
|
|
|
DBA
|
[NCBI]
|
1.136148e-05
|
|
|
MTR
|
[NCBI]
|
1.131492e-05
|
|
|
FTD
|
[NCBI]
|
1.106887e-05
|
|
|
COL1A2
|
[NCBI]
|
1.064882e-05
|
|
|
ZS
|
[NCBI]
|
1.063525e-05
|
|
|
PABPC1
|
[NCBI]
|
1.025942e-05
|
|
|
GCK
|
[NCBI]
|
1.025009e-05
|
|
|
CP
|
[NCBI]
|
9.51287e-06
|
|
|
LMNA
|
[NCBI]
|
9.50531e-06
|
|
|
homocystinuria
|
[NCBI]
|
9.39835e-06
|
|
|
GH1
|
[NCBI]
|
9.26382e-06
|
|
|
MYOC
|
[NCBI]
|
9.11394e-06
|
|
|
PCD
|
[NCBI]
|
9.01516e-06
|
|
|
MC1R
|
[NCBI]
|
8.99539e-06
|
|
|
MAOA
|
[NCBI]
|
8.47953e-06
|
|
|
ABCC8
|
[NCBI]
|
7.81516e-06
|
|
|
DHFR
|
[NCBI]
|
7.54996e-06
|
|
|
CPI
|
[NCBI]
|
6.568604e-06
|
|
|
VASP
|
[NCBI]
|
5.78997e-06
|
|
|
TERT
|
[NCBI]
|
5.51976e-06
|
|
|
polycystic kidneys
|
[NCBI]
|
5.32634e-06
|
|
|
CASR
|
[NCBI]
|
5.3205e-06
|
|
|
DGS
|
[NCBI]
|
5.225505e-06
|
|
|
AR
|
[NCBI]
|
5.19344e-06
|
|
|
ACADM
|
[NCBI]
|
5.10345e-06
|
|
|
HEMB
|
[NCBI]
|
4.5417e-06
|
|
|
PMD
|
[NCBI]
|
4.50562e-06
|
|
|
ADA
|
[NCBI]
|
4.32534e-06
|
|
|
ILK
|
[NCBI]
|
3.2105e-06
|
|
|
FA
|
[NCBI]
|
2.69122e-06
|
|
|
SHH
|
[NCBI]
|
2.415248e-06
|
|
|
HBB
|
[NCBI]
|
2.18874e-06
|
|
|
TP53
|
[NCBI]
|
2.163514e-06
|
|
|
LPL
|
[NCBI]
|
1.613339e-06
|
|
|
GAPDH
|
[NCBI]
|
1.527066e-06
|
|
|
HBA1
|
[NCBI]
|
1.38297e-06
|
|
|
AT
|
[NCBI]
|
1.197553e-06
|
|
|
BWS
|
[NCBI]
|
1.077107e-06
|
|
|
STAR
|
[NCBI]
|
1.000427e-06
|
|
|
LDLR
|
[NCBI]
|
9.84678e-07
|
|
|
SLOS
|
[NCBI]
|
9.78217e-07
|
|
|
VDR
|
[NCBI]
|
8.90966e-07
|
|
|
FMF
|
[NCBI]
|
5.303474e-07
|
|
|
ADCYAP1
|
[NCBI]
|
4.70013e-07
|
|
|
TG
|
[NCBI]
|
2.6970552e-07
|
|
|
GHRH
|
[NCBI]
|
1.950348e-07
|
|
|
APOB
|
[NCBI]
|
1.357236e-07
|
|
|
SRF
|
[NCBI]
|
1.229215e-07
|
|
|
TLR4
|
[NCBI]
|
3.16238e-08
|
|