|
OMIM |
Link |
Information gain |
01 |
|
SLOS
|
[NCBI]
|
0.00345835
|
|
|
saccharopinuria
|
[NCBI]
|
0.00308494
|
|
|
myopathy with deficiency of succinate dehydrogenase and aconitase
|
[NCBI]
|
0.00277652
|
|
|
glaucoma-related pigment dispersion syndrome
|
[NCBI]
|
0.00255997
|
|
|
porphyria variegata
|
[NCBI]
|
0.00254214
|
|
|
tricarboxylic acid cycle, defect of
|
[NCBI]
|
0.00216024
|
|
|
graying of hair, precocious
|
[NCBI]
|
0.00216024
|
|
|
CLN9
|
[NCBI]
|
0.00163815
|
|
|
glutaric acidemia i
|
[NCBI]
|
0.00137729
|
|
|
antipyrine metabolism
|
[NCBI]
|
0.00131475
|
|
|
CAT
|
[NCBI]
|
0.00127577
|
|
|
IVA
|
[NCBI]
|
0.00122925
|
|
|
RA
|
[NCBI]
|
0.00117331
|
|
|
CYP1A1
|
[NCBI]
|
0.00100927
|
|
|
PPSH
|
[NCBI]
|
0.000999067
|
|
|
bile acid synthesis defect, congenital, 2
|
[NCBI]
|
0.000985043
|
|
|
wernicke-korsakoff syndrome
|
[NCBI]
|
0.000984686
|
|
|
beta-aminoisobutyric acid, urinary excretion of
|
[NCBI]
|
0.000907228
|
|
|
SLE
|
[NCBI]
|
0.000832574
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
0.000788857
|
|
|
CMM
|
[NCBI]
|
0.000702867
|
|
|
DPYD
|
[NCBI]
|
0.000655399
|
|
|
peroxisomal acyl-coa oxidase deficiency
|
[NCBI]
|
0.000635991
|
|
|
PPOX
|
[NCBI]
|
0.000626061
|
|
|
sulfocysteinuria
|
[NCBI]
|
0.000534554
|
|
|
IVD
|
[NCBI]
|
0.000516444
|
|
|
TYRP1
|
[NCBI]
|
0.00051427
|
|
|
PGL1
|
[NCBI]
|
0.000511555
|
|
|
GCDH
|
[NCBI]
|
0.000486366
|
|
|
DHCR7
|
[NCBI]
|
0.000462533
|
|
|
ACOX1
|
[NCBI]
|
0.000459007
|
|
|
TYMS
|
[NCBI]
|
0.000395655
|
|
|
mitochondrial complex ii deficiency
|
[NCBI]
|
0.000383258
|
|
|
TYR
|
[NCBI]
|
0.000301396
|
|
|
hydrops-ectopic calcification-moth-eaten skeletal dysplasia
|
[NCBI]
|
0.000274331
|
|
|
desmosterolosis
|
[NCBI]
|
0.000274331
|
|
|
CF
|
[NCBI]
|
0.000273467
|
|
|
d-bifunctional protein deficiency
|
[NCBI]
|
0.000270595
|
|
|
pheochromocytoma
|
[NCBI]
|
0.000265465
|
|
|
OCA3
|
[NCBI]
|
0.000248704
|
|
|
SDHD
|
[NCBI]
|
0.000248282
|
|
|
molybdenum cofactor deficiency
|
[NCBI]
|
0.000247523
|
|
|
DCT
|
[NCBI]
|
0.000242836
|
|
|
P4HB
|
[NCBI]
|
0.000201429
|
|
|
17-@beta hydroxysteroid dehydrogenase iii deficiency
|
[NCBI]
|
0.000194184
|
|
|
2-@methylbutyryl-coa dehydrogenase deficiency
|
[NCBI]
|
0.000182809
|
|
|
ZS
|
[NCBI]
|
0.000174573
|
|
|
WWOX
|
[NCBI]
|
0.00016825
|
|
|
OCA2
|
[NCBI]
|
0.000164901
|
|
|
refsum disease, infantile form
|
[NCBI]
|
0.000164901
|
|
|
BLVRA
|
[NCBI]
|
0.000161236
|
|
|
MITF
|
[NCBI]
|
0.00015847
|
|
|
hemochromatosis, neonatal
|
[NCBI]
|
0.000150868
|
|
|
HPS
|
[NCBI]
|
0.000144924
|
|
|
reifenstein syndrome
|
[NCBI]
|
0.000143889
|
|
|
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
[NCBI]
|
0.000143889
|
|
|
VEGF
|
[NCBI]
|
0.000138289
|
|
|
SDHC
|
[NCBI]
|
0.000134229
|
|
|
hyperprolinemia, type ii
|
[NCBI]
|
0.000127864
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
0.000124975
|
|
|
MTHFR
|
[NCBI]
|
0.000124947
|
|
|
AKR1D1
|
[NCBI]
|
0.000123503
|
|
|
GLRX2
|
[NCBI]
|
0.000123503
|
|
|
MSRA
|
[NCBI]
|
0.000123503
|
|
|
myopathy with giant abnormal mitochondria
|
[NCBI]
|
0.000122853
|
|
|
ROCA
|
[NCBI]
|
0.000122853
|
|
|
methemoglobin reductase deficiency
|
[NCBI]
|
0.000122853
|
|
|
mitochondrial myopathy with a defect in mitochondrial-protein transport
|
[NCBI]
|
0.000122853
|
|
|
CP
|
[NCBI]
|
0.000111408
|
|
|
RDH11
|
[NCBI]
|
0.000110122
|
|
|
SC5DL
|
[NCBI]
|
0.000110122
|
|
|
SLC39A7
|
[NCBI]
|
0.000110122
|
|
|
ABS
|
[NCBI]
|
0.00010986
|
|
|
lipoid congenital adrenal hyperplasia
|
[NCBI]
|
0.00010986
|
|
|
corticosterone methyloxidase type ii deficiency
|
[NCBI]
|
0.000107018
|
|
|
XDH
|
[NCBI]
|
0.000102111
|
|
|
CDPX2
|
[NCBI]
|
9.94875e-05
|
|
|
alopecia, androgenetic
|
[NCBI]
|
9.81598e-05
|
|
|
AKR1C1
|
[NCBI]
|
9.79547e-05
|
|
|
CYP1A2
|
[NCBI]
|
9.76616e-05
|
|
|
PPARA
|
[NCBI]
|
9.709e-05
|
|
|
CGD
|
[NCBI]
|
9.43959e-05
|
|
|
GLRX
|
[NCBI]
|
9.26177e-05
|
|
|
ACOX2
|
[NCBI]
|
9.26177e-05
|
|
|
dystonia, familial, with visual failure and striatal lucencies
|
[NCBI]
|
9.13656e-05
|
|
|
urocanase deficiency
|
[NCBI]
|
9.13656e-05
|
|
|
glutaryl-coa oxidase deficiency
|
[NCBI]
|
9.13656e-05
|
|
|
carcinoid tumors, intestinal
|
[NCBI]
|
9.13656e-05
|
|
|
AKR1C2
|
[NCBI]
|
9.0479e-05
|
|
|
PRL
|
[NCBI]
|
8.91163e-05
|
|
|
SRD5A2
|
[NCBI]
|
8.65866e-05
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i
|
[NCBI]
|
8.42901e-05
|
|
|
LBR
|
[NCBI]
|
8.17476e-05
|
|
|
HSD17B8
|
[NCBI]
|
8.05894e-05
|
|
|
hypospadias, x-linked
|
[NCBI]
|
7.95456e-05
|
|
|
TYRL
|
[NCBI]
|
7.95456e-05
|
|
|
PGL3
|
[NCBI]
|
7.95456e-05
|
|
|
SDHB
|
[NCBI]
|
7.55238e-05
|
|
|
MADD
|
[NCBI]
|
7.32871e-05
|
|
|
NGFB
|
[NCBI]
|
7.23037e-05
|
|
|
lathosterolosis
|
[NCBI]
|
7.19062e-05
|
|
|
EGF
|
[NCBI]
|
7.00325e-05
|
|
|
hydroxyprolinemia
|
[NCBI]
|
6.62522e-05
|
|
|
NPY
|
[NCBI]
|
6.49795e-05
|
|
|
AKR1C4
|
[NCBI]
|
6.43606e-05
|
|
|
SDHA
|
[NCBI]
|
6.43606e-05
|
|
|
KSS
|
[NCBI]
|
6.26307e-05
|
|
|
OCA4
|
[NCBI]
|
6.17676e-05
|
|
|
indifference to pain, congenital, autosomal recessive
|
[NCBI]
|
6.17676e-05
|
|
|
G6PD
|
[NCBI]
|
6.00858e-05
|
|
|
EGFR
|
[NCBI]
|
5.80951e-05
|
|
|
LGMD2H
|
[NCBI]
|
5.80557e-05
|
|
|
mitochondrial myopathy
|
[NCBI]
|
5.80557e-05
|
|
|
AEXS
|
[NCBI]
|
5.80557e-05
|
|
|
AHR
|
[NCBI]
|
5.65282e-05
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
5.2646e-05
|
|
|
CHS
|
[NCBI]
|
5.25931e-05
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-negative
|
[NCBI]
|
5.21409e-05
|
|
|
RHN
|
[NCBI]
|
5.21409e-05
|
|
|
sarcosinemia
|
[NCBI]
|
5.21409e-05
|
|
|
STEAP
|
[NCBI]
|
5.15302e-05
|
|
|
BLVRB
|
[NCBI]
|
5.15302e-05
|
|
|
CYBRD1
|
[NCBI]
|
5.15302e-05
|
|
|
TNF
|
[NCBI]
|
5.02261e-05
|
|
|
l-2-hydroxyglutaric aciduria
|
[NCBI]
|
4.97076e-05
|
|
|
por deficiency
|
[NCBI]
|
4.97076e-05
|
|
|
gtp cyclohydrolase i deficiency
|
[NCBI]
|
4.97076e-05
|
|
|
PHA
|
[NCBI]
|
4.75288e-05
|
|
|
hyperlysinemia
|
[NCBI]
|
4.75288e-05
|
|
|
AIS
|
[NCBI]
|
4.57692e-05
|
|
|
methemoglobinemia due to deficiency of methemoglobin reductase
|
[NCBI]
|
4.47163e-05
|
|
|
GAPDH
|
[NCBI]
|
4.40392e-05
|
|
|
ACADSB
|
[NCBI]
|
4.37696e-05
|
|
|
MERRF
|
[NCBI]
|
4.3761e-05
|
|
|
IFD
|
[NCBI]
|
4.3761e-05
|
|
|
CMM2
|
[NCBI]
|
4.3761e-05
|
|
|
leber optic atrophy
|
[NCBI]
|
4.35204e-05
|
|
|
GFAP
|
[NCBI]
|
4.16799e-05
|
|
|
AKR1C3
|
[NCBI]
|
3.9397e-05
|
|
|
LS
|
[NCBI]
|
3.84597e-05
|
|
|
xanthinuria, type i
|
[NCBI]
|
3.78474e-05
|
|
|
aceruloplasminemia
|
[NCBI]
|
3.78474e-05
|
|
|
TH
|
[NCBI]
|
3.78092e-05
|
|
|
PDIA3
|
[NCBI]
|
3.77495e-05
|
|
|
FRDA
|
[NCBI]
|
3.67541e-05
|
|
|
methionine adenosyltransferase deficiency
|
[NCBI]
|
3.661e-05
|
|
|
neural tube defects, folate-sensitive
|
[NCBI]
|
3.661e-05
|
|
|
SPTLC1
|
[NCBI]
|
3.63276e-05
|
|
|
SOD2
|
[NCBI]
|
3.59026e-05
|
|
|
neural tube defects
|
[NCBI]
|
3.54473e-05
|
|
|
BDNF
|
[NCBI]
|
3.51567e-05
|
|
|
CRC
|
[NCBI]
|
3.45441e-05
|
|
|
PEX12
|
[NCBI]
|
3.39612e-05
|
|
|
SOD1
|
[NCBI]
|
3.38379e-05
|
|
|
sitosterolemia
|
[NCBI]
|
3.33154e-05
|
|
|
thyroid hormonogenesis, genetic defect in, 2a
|
[NCBI]
|
3.33154e-05
|
|
|
CRH
|
[NCBI]
|
3.23633e-05
|
|
|
UOX
|
[NCBI]
|
3.23338e-05
|
|
|
GSR
|
[NCBI]
|
3.20209e-05
|
|
|
MELAS
|
[NCBI]
|
3.14015e-05
|
|
|
AVP
|
[NCBI]
|
3.10788e-05
|
|
|
CYP51A1
|
[NCBI]
|
3.08663e-05
|
|
|
orphan short-chain dehydrogenase/reductase
|
[NCBI]
|
3.08663e-05
|
|
|
HIBADH
|
[NCBI]
|
3.08663e-05
|
|
|
mem3, mouse, homolog of
|
[NCBI]
|
3.08663e-05
|
|
|
DUS2L
|
[NCBI]
|
3.08663e-05
|
|
|
ATG10
|
[NCBI]
|
3.08663e-05
|
|
|
ACOX3
|
[NCBI]
|
3.08663e-05
|
|
|
flavoprotein oxidoreductase mical3
|
[NCBI]
|
3.08663e-05
|
|
|
TM7SF2
|
[NCBI]
|
3.08663e-05
|
|
|
DHDH
|
[NCBI]
|
3.08663e-05
|
|
|
FRRS1
|
[NCBI]
|
3.08663e-05
|
|
|
DHODH
|
[NCBI]
|
3.08663e-05
|
|
|
AASDHPPT
|
[NCBI]
|
3.08663e-05
|
|
|
refsum disease
|
[NCBI]
|
3.05143e-05
|
|
|
KLK3
|
[NCBI]
|
3.02877e-05
|
|
|
HEPH
|
[NCBI]
|
2.96928e-05
|
|
|
MTHFD1
|
[NCBI]
|
2.96928e-05
|
|
|
VIP
|
[NCBI]
|
2.96168e-05
|
|
|
SLC45A2
|
[NCBI]
|
2.90174e-05
|
|
|
NR5A2
|
[NCBI]
|
2.83841e-05
|
|
|
CYP11A1
|
[NCBI]
|
2.83841e-05
|
|
|
MAP3K5
|
[NCBI]
|
2.81074e-05
|
|
|
POAG
|
[NCBI]
|
2.80879e-05
|
|
|
CYP19A1
|
[NCBI]
|
2.7644e-05
|
|
|
ALGS1
|
[NCBI]
|
2.73477e-05
|
|
|
HSD17B4
|
[NCBI]
|
2.66923e-05
|
|
|
OCA1A
|
[NCBI]
|
2.66376e-05
|
|
|
MBP
|
[NCBI]
|
2.65776e-05
|
|
|
GFER
|
[NCBI]
|
2.48055e-05
|
|
|
acyl-coa dehydrogenase, medium-chain, deficiency of
|
[NCBI]
|
2.46685e-05
|
|
|
H6PD
|
[NCBI]
|
2.34806e-05
|
|
|
glutaredoxin 5
|
[NCBI]
|
2.34596e-05
|
|
|
EHHADH
|
[NCBI]
|
2.34596e-05
|
|
|
C11ORF5
|
[NCBI]
|
2.34596e-05
|
|
|
RAB38
|
[NCBI]
|
2.34596e-05
|
|
|
NICAL
|
[NCBI]
|
2.34596e-05
|
|
|
NCB5OR
|
[NCBI]
|
2.34596e-05
|
|
|
flavoprotein oxidoreductase mical2
|
[NCBI]
|
2.34596e-05
|
|
|
STEAP4
|
[NCBI]
|
2.34596e-05
|
|
|
IFI30
|
[NCBI]
|
2.34596e-05
|
|
|
LPL
|
[NCBI]
|
2.33557e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
2.30035e-05
|
|
|
mitochondrial complex iv deficiency
|
[NCBI]
|
2.236e-05
|
|
|
drug metabolism, poor, cyp2d6-related
|
[NCBI]
|
2.236e-05
|
|
|
mitochondrial complex i deficiency
|
[NCBI]
|
2.0823e-05
|
|
|
ACHE
|
[NCBI]
|
2.07777e-05
|
|
|
STEAP3
|
[NCBI]
|
2.06744e-05
|
|
|
SEPX1
|
[NCBI]
|
2.06744e-05
|
|
|
TIMM8B
|
[NCBI]
|
2.06744e-05
|
|
|
CYB561
|
[NCBI]
|
2.06744e-05
|
|
|
SESN2
|
[NCBI]
|
2.06744e-05
|
|
|
NDOR1
|
[NCBI]
|
2.06744e-05
|
|
|
AADAC
|
[NCBI]
|
2.06744e-05
|
|
|
ACAD8
|
[NCBI]
|
2.06744e-05
|
|
|
coproporphyria
|
[NCBI]
|
1.91125e-05
|
|
|
prostate cancer
|
[NCBI]
|
1.89863e-05
|
|
|
ALD
|
[NCBI]
|
1.8908e-05
|
|
|
GPNMB
|
[NCBI]
|
1.88716e-05
|
|
|
DCPS
|
[NCBI]
|
1.88716e-05
|
|
|
d-2-@hydroxyglutarate dehydrogenase
|
[NCBI]
|
1.88716e-05
|
|
|
ALDH1A3
|
[NCBI]
|
1.88716e-05
|
|
|
MTCYB
|
[NCBI]
|
1.86477e-05
|
|
|
SCP2
|
[NCBI]
|
1.75789e-05
|
|
|
RING1
|
[NCBI]
|
1.75354e-05
|
|
|
MTHFD2
|
[NCBI]
|
1.75354e-05
|
|
|
PRDX3
|
[NCBI]
|
1.75354e-05
|
|
|
L2HGDH
|
[NCBI]
|
1.75354e-05
|
|
|
SESN1
|
[NCBI]
|
1.75354e-05
|
|
|
DPYS
|
[NCBI]
|
1.6474e-05
|
|
|
AOX1
|
[NCBI]
|
1.6474e-05
|
|
|
DHCR24
|
[NCBI]
|
1.6474e-05
|
|
|
GIF
|
[NCBI]
|
1.6474e-05
|
|
|
TRIM32
|
[NCBI]
|
1.55942e-05
|
|
|
MDH2
|
[NCBI]
|
1.55942e-05
|
|
|
CTBP2
|
[NCBI]
|
1.55942e-05
|
|
|
CFL1
|
[NCBI]
|
1.55942e-05
|
|
|
TRMU
|
[NCBI]
|
1.55942e-05
|
|
|
CDSP
|
[NCBI]
|
1.55448e-05
|
|
|
MTTE
|
[NCBI]
|
1.48434e-05
|
|
|
KLF3
|
[NCBI]
|
1.48434e-05
|
|
|
SRD5A1
|
[NCBI]
|
1.48434e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
1.46745e-05
|
|
|
NIDDM
|
[NCBI]
|
1.45665e-05
|
|
|
PEX6
|
[NCBI]
|
1.41891e-05
|
|
|
PRDX2
|
[NCBI]
|
1.41891e-05
|
|
|
ACADM
|
[NCBI]
|
1.36667e-05
|
|
|
T
|
[NCBI]
|
1.36097e-05
|
|
|
DDB1
|
[NCBI]
|
1.30901e-05
|
|
|
HPD
|
[NCBI]
|
1.30901e-05
|
|
|
PHYH
|
[NCBI]
|
1.30901e-05
|
|
|
MDH1
|
[NCBI]
|
1.30901e-05
|
|
|
MDM1
|
[NCBI]
|
1.30901e-05
|
|
|
POR
|
[NCBI]
|
1.30901e-05
|
|
|
GSS
|
[NCBI]
|
1.26194e-05
|
|
|
NPC1
|
[NCBI]
|
1.22773e-05
|
|
|
VHL
|
[NCBI]
|
1.22773e-05
|
|
|
OTX2
|
[NCBI]
|
1.21895e-05
|
|
|
SLC11A2
|
[NCBI]
|
1.20686e-05
|
|
|
cortisol 11-beta-ketoreductase deficiency
|
[NCBI]
|
1.20686e-05
|
|
|
IDH1
|
[NCBI]
|
1.1794e-05
|
|
|
PRDX5
|
[NCBI]
|
1.1794e-05
|
|
|
PFKL
|
[NCBI]
|
1.1428e-05
|
|
|
GNPAT
|
[NCBI]
|
1.1428e-05
|
|
|
CYBA
|
[NCBI]
|
1.1428e-05
|
|
|
SCA1
|
[NCBI]
|
1.12796e-05
|
|
|
ANTXR1
|
[NCBI]
|
1.10876e-05
|
|
|
KEAP1
|
[NCBI]
|
1.10876e-05
|
|
|
VDR
|
[NCBI]
|
1.07889e-05
|
|
|
MPI
|
[NCBI]
|
1.07695e-05
|
|
|
MAT1A
|
[NCBI]
|
1.07695e-05
|
|
|
BTRC
|
[NCBI]
|
1.04711e-05
|
|
|
UGDH
|
[NCBI]
|
1.04711e-05
|
|
|
TG
|
[NCBI]
|
1.0303e-05
|
|
|
PGD
|
[NCBI]
|
9.92515e-06
|
|
|
EBP
|
[NCBI]
|
9.92515e-06
|
|
|
PKD1
|
[NCBI]
|
9.7835e-06
|
|
|
PPARD
|
[NCBI]
|
9.67412e-06
|
|
|
3-@beta-hydroxysteroid dehydrogenase, type ii, deficiency of
|
[NCBI]
|
9.43585e-06
|
|
|
CCL25
|
[NCBI]
|
9.43585e-06
|
|
|
DHFR
|
[NCBI]
|
9.22684e-06
|
|
|
MAPK8
|
[NCBI]
|
8.78674e-06
|
|
|
orotic aciduria i
|
[NCBI]
|
8.78674e-06
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
8.74733e-06
|
|
|
PTK2
|
[NCBI]
|
8.70385e-06
|
|
|
RET
|
[NCBI]
|
8.62231e-06
|
|
|
CBD
|
[NCBI]
|
8.21857e-06
|
|
|
DLD
|
[NCBI]
|
8.04411e-06
|
|
|
oca2 gene
|
[NCBI]
|
8.04411e-06
|
|
|
phenylketonuria ii
|
[NCBI]
|
8.04411e-06
|
|
|
AR
|
[NCBI]
|
7.66011e-06
|
|
|
GCH1
|
[NCBI]
|
7.55859e-06
|
|
|
MTND6
|
[NCBI]
|
7.55859e-06
|
|
|
SLC40A1
|
[NCBI]
|
7.26257e-06
|
|
|
HPX
|
[NCBI]
|
7.26257e-06
|
|
|
MTND5
|
[NCBI]
|
7.26257e-06
|
|
|
MTRNR1
|
[NCBI]
|
7.26257e-06
|
|
|
MTTK
|
[NCBI]
|
7.12187e-06
|
|
|
GPX1
|
[NCBI]
|
7.12187e-06
|
|
|
krabbe disease
|
[NCBI]
|
7.05532e-06
|
|
|
CYP2A6
|
[NCBI]
|
6.6017e-06
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
6.36414e-06
|
|
|
ATF2
|
[NCBI]
|
6.36414e-06
|
|
|
CYP3A4
|
[NCBI]
|
6.25034e-06
|
|
|
wilson disease
|
[NCBI]
|
6.18479e-06
|
|
|
PSCA
|
[NCBI]
|
5.62815e-06
|
|
|
ZNF145
|
[NCBI]
|
5.62815e-06
|
|
|
AMACR
|
[NCBI]
|
5.53341e-06
|
|
|
SPP1
|
[NCBI]
|
5.47528e-06
|
|
|
RHCE
|
[NCBI]
|
5.44094e-06
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
5.17632e-06
|
|
|
FXN
|
[NCBI]
|
5.17632e-06
|
|
|
RIPK1
|
[NCBI]
|
5.0921e-06
|
|
|
ALAD
|
[NCBI]
|
4.92921e-06
|
|
|
TFRC
|
[NCBI]
|
4.77328e-06
|
|
|
DAO
|
[NCBI]
|
4.62384e-06
|
|
|
MTND4
|
[NCBI]
|
4.34272e-06
|
|
|
ABP1
|
[NCBI]
|
3.85728e-06
|
|
|
NR0B2
|
[NCBI]
|
3.56408e-06
|
|
|
VHL
|
[NCBI]
|
3.56408e-06
|
|
|
MTTL1
|
[NCBI]
|
3.51136e-06
|
|
|
ABCC1
|
[NCBI]
|
3.32538e-06
|
|
|
COMT
|
[NCBI]
|
3.18985e-06
|
|
|
ARNT
|
[NCBI]
|
3.02974e-06
|
|
|
MTR
|
[NCBI]
|
3.02974e-06
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.98572e-06
|
|
|
PDCD8
|
[NCBI]
|
2.83794e-06
|
|
|
AKR1B1
|
[NCBI]
|
2.12207e-06
|
|
|
CDKN2A
|
[NCBI]
|
2.0741e-06
|
|
|
homocystinuria
|
[NCBI]
|
2.0741e-06
|
|
|
PIGR
|
[NCBI]
|
1.95595e-06
|
|
|
PC
|
[NCBI]
|
1.81694e-06
|
|
|
SHBG
|
[NCBI]
|
1.64869e-06
|
|
|
PAM
|
[NCBI]
|
1.61281e-06
|
|
|
ABCC8
|
[NCBI]
|
1.58876e-06
|
|
|
GPI
|
[NCBI]
|
1.48815e-06
|
|
|
APC
|
[NCBI]
|
1.42038e-06
|
|
|
UCP1
|
[NCBI]
|
1.26278e-06
|
|
|
HBA2
|
[NCBI]
|
1.24319e-06
|
|
|
LPO
|
[NCBI]
|
1.18586e-06
|
|
|
FGF2
|
[NCBI]
|
1.00968e-06
|
|
|
HMBS
|
[NCBI]
|
9.45192e-07
|
|
|
TF
|
[NCBI]
|
9.06063e-07
|
|
|
MB
|
[NCBI]
|
9.01413e-07
|
|
|
DBI
|
[NCBI]
|
8.25562e-07
|
|
|
NF1
|
[NCBI]
|
5.11441e-07
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
5.01366e-07
|
|
|
ACPP
|
[NCBI]
|
2.14267e-07
|
|
|
INS
|
[NCBI]
|
7.84756e-08
|
|
|
MPO
|
[NCBI]
|
5.88042e-08
|
|
|
HDC
|
[NCBI]
|
1.77047e-08
|
|
|
AMH
|
[NCBI]
|
5.71506e-09
|
|
|
NR1I2
|
[NCBI]
|
1.12044e-09
|
|