|
OMIM |
Link |
Information gain |
01 |
|
PCLD
|
[NCBI]
|
0.00217505
|
|
|
ATD1
|
[NCBI]
|
0.00149618
|
|
|
AFP
|
[NCBI]
|
0.00103833
|
|
|
ORW3
|
[NCBI]
|
0.000725612
|
|
|
leri pleonosteosis
|
[NCBI]
|
0.000672411
|
|
|
eosinophilia, familial
|
[NCBI]
|
0.000632907
|
|
|
MKS2
|
[NCBI]
|
0.000601472
|
|
|
ZS
|
[NCBI]
|
0.000583971
|
|
|
arima syndrome
|
[NCBI]
|
0.000553054
|
|
|
pulmonary alveolar proteinosis, acquired
|
[NCBI]
|
0.00051629
|
|
|
PI
|
[NCBI]
|
0.00050459
|
|
|
polycystic kidneys
|
[NCBI]
|
0.000404804
|
|
|
DHS
|
[NCBI]
|
0.000397762
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.000376956
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
0.000364561
|
|
|
ALAD
|
[NCBI]
|
0.000352275
|
|
|
GPT
|
[NCBI]
|
0.000338269
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
0.000323443
|
|
|
CF
|
[NCBI]
|
0.00031549
|
|
|
HHT
|
[NCBI]
|
0.000293715
|
|
|
ARPKD
|
[NCBI]
|
0.000288872
|
|
|
retinohepatoendocrinologic syndrome
|
[NCBI]
|
0.000273172
|
|
|
HGF
|
[NCBI]
|
0.000268067
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000254316
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
0.000221713
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
0.000218128
|
|
|
porphyria variegata
|
[NCBI]
|
0.000210603
|
|
|
NN
|
[NCBI]
|
0.000195915
|
|
|
MPV17
|
[NCBI]
|
0.00018295
|
|
|
CAT
|
[NCBI]
|
0.000162483
|
|
|
carnitine palmitoyltransferase ii deficiency, infantile
|
[NCBI]
|
0.000137237
|
|
|
gilbert syndrome
|
[NCBI]
|
0.000132239
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
0.000128333
|
|
|
cerebellar vermis aplasia with associated features suggesting smith-lemli-opitz syndrome and meckel syndrome
|
[NCBI]
|
0.000127692
|
|
|
TNF
|
[NCBI]
|
0.000123355
|
|
|
arthrogryposis, renal dysfunction, and cholestasis
|
[NCBI]
|
0.000109492
|
|
|
hyperpipecolatemia
|
[NCBI]
|
0.000109492
|
|
|
PFIC1
|
[NCBI]
|
0.000109092
|
|
|
CEACAM5
|
[NCBI]
|
0.000107337
|
|
|
tyrosinemia, type i
|
[NCBI]
|
0.000101676
|
|
|
CDG1B
|
[NCBI]
|
0.000101418
|
|
|
KLK3
|
[NCBI]
|
9.90274e-05
|
|
|
AD
|
[NCBI]
|
9.16091e-05
|
|
|
PRKCSH
|
[NCBI]
|
9.144e-05
|
|
|
granulomatous disease due to combined cellular and humoral immune defects
|
[NCBI]
|
9.10074e-05
|
|
|
hyperzincemia with functional zinc depletion
|
[NCBI]
|
9.10074e-05
|
|
|
ALB
|
[NCBI]
|
8.93782e-05
|
|
|
TNFSF6
|
[NCBI]
|
8.9058e-05
|
|
|
mitochondrial dna depletion syndrome, hepatocerebral form
|
[NCBI]
|
8.51672e-05
|
|
|
MKS1
|
[NCBI]
|
8.34392e-05
|
|
|
VEGF
|
[NCBI]
|
8.15245e-05
|
|
|
JH
|
[NCBI]
|
7.94256e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
7.31499e-05
|
|
|
PRL
|
[NCBI]
|
7.2256e-05
|
|
|
MPO
|
[NCBI]
|
7.13387e-05
|
|
|
RA
|
[NCBI]
|
6.99281e-05
|
|
|
HFE
|
[NCBI]
|
6.9096e-05
|
|
|
VODI
|
[NCBI]
|
6.85939e-05
|
|
|
axial osteomalacia
|
[NCBI]
|
6.85939e-05
|
|
|
dwarfism with stiff joints and ocular abnormalities
|
[NCBI]
|
6.85939e-05
|
|
|
glycogen storage disease iv
|
[NCBI]
|
6.46014e-05
|
|
|
LCA1
|
[NCBI]
|
6.35608e-05
|
|
|
MPI
|
[NCBI]
|
6.09486e-05
|
|
|
GBE1
|
[NCBI]
|
6.09486e-05
|
|
|
GEMSS
|
[NCBI]
|
6.01708e-05
|
|
|
omphalocele, diaphragmatic hernia, and radial ray defects
|
[NCBI]
|
6.01708e-05
|
|
|
ceroid storage disease
|
[NCBI]
|
6.01708e-05
|
|
|
glycogen storage disease iii
|
[NCBI]
|
5.97374e-05
|
|
|
wolman disease
|
[NCBI]
|
5.83094e-05
|
|
|
EGF
|
[NCBI]
|
5.70571e-05
|
|
|
wilson disease
|
[NCBI]
|
5.59478e-05
|
|
|
CPT2
|
[NCBI]
|
5.53268e-05
|
|
|
ABCB4
|
[NCBI]
|
5.53268e-05
|
|
|
CYP7B1
|
[NCBI]
|
5.5183e-05
|
|
|
TRAM2
|
[NCBI]
|
5.5183e-05
|
|
|
SAA4
|
[NCBI]
|
5.5183e-05
|
|
|
melanoma inhibitory activity protein 2
|
[NCBI]
|
5.5183e-05
|
|
|
CENPE
|
[NCBI]
|
5.5183e-05
|
|
|
coach syndrome
|
[NCBI]
|
5.47216e-05
|
|
|
bile acid synthesis defect, congenital, 1
|
[NCBI]
|
5.06848e-05
|
|
|
osteomesopyknosis
|
[NCBI]
|
5.06848e-05
|
|
|
bile acid synthesis defect, congenital, 4
|
[NCBI]
|
5.06848e-05
|
|
|
hawkinsinuria
|
[NCBI]
|
5.06848e-05
|
|
|
HNF1A
|
[NCBI]
|
4.93939e-05
|
|
|
MG
|
[NCBI]
|
4.82095e-05
|
|
|
australia antigen
|
[NCBI]
|
4.74798e-05
|
|
|
phosphorylase kinase deficiency of liver and muscle, autosomal recessive
|
[NCBI]
|
4.74798e-05
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
4.7021e-05
|
|
|
PTH
|
[NCBI]
|
4.56534e-05
|
|
|
porphyria cutanea tarda, type i
|
[NCBI]
|
4.48245e-05
|
|
|
glycogen storage disease 0, liver
|
[NCBI]
|
4.48245e-05
|
|
|
EGFR
|
[NCBI]
|
4.39668e-05
|
|
|
carnitine palmitoyltransferase i deficiency
|
[NCBI]
|
4.25599e-05
|
|
|
budd-chiari syndrome
|
[NCBI]
|
4.25599e-05
|
|
|
ARIX
|
[NCBI]
|
4.14409e-05
|
|
|
UGT1A9
|
[NCBI]
|
4.14409e-05
|
|
|
MTF1
|
[NCBI]
|
4.14409e-05
|
|
|
VTN
|
[NCBI]
|
4.14409e-05
|
|
|
XYLT2
|
[NCBI]
|
4.14409e-05
|
|
|
PCTP
|
[NCBI]
|
4.14409e-05
|
|
|
ALGS1
|
[NCBI]
|
3.8852e-05
|
|
|
growth-mental deficiency syndrome of myhre
|
[NCBI]
|
3.88416e-05
|
|
|
HES
|
[NCBI]
|
3.88416e-05
|
|
|
EPO
|
[NCBI]
|
3.85212e-05
|
|
|
PDV
|
[NCBI]
|
3.7277e-05
|
|
|
gracile syndrome
|
[NCBI]
|
3.7277e-05
|
|
|
PCNA
|
[NCBI]
|
3.7039e-05
|
|
|
HSD3B7
|
[NCBI]
|
3.62781e-05
|
|
|
PROX1
|
[NCBI]
|
3.62781e-05
|
|
|
fructose-1,6-bisphosphatase deficiency
|
[NCBI]
|
3.58604e-05
|
|
|
crigler-najjar syndrome, type ii
|
[NCBI]
|
3.58604e-05
|
|
|
BRIC1
|
[NCBI]
|
3.45671e-05
|
|
|
hepatitis c virus, susceptibility to
|
[NCBI]
|
3.45671e-05
|
|
|
SLC2A2
|
[NCBI]
|
3.43902e-05
|
|
|
CYP1A1
|
[NCBI]
|
3.34599e-05
|
|
|
mitochondrial dna depletion syndrome, myopathic form
|
[NCBI]
|
3.3378e-05
|
|
|
PHKB
|
[NCBI]
|
3.29389e-05
|
|
|
KRT18
|
[NCBI]
|
3.29389e-05
|
|
|
TRAF1
|
[NCBI]
|
3.29389e-05
|
|
|
CYP2R1
|
[NCBI]
|
3.29389e-05
|
|
|
PKD2L1
|
[NCBI]
|
3.29389e-05
|
|
|
NPY
|
[NCBI]
|
3.27203e-05
|
|
|
d-bifunctional protein deficiency
|
[NCBI]
|
3.22783e-05
|
|
|
PKD1
|
[NCBI]
|
3.15218e-05
|
|
|
IGF2BP2
|
[NCBI]
|
3.04658e-05
|
|
|
ADORA2A
|
[NCBI]
|
3.04658e-05
|
|
|
PCK2
|
[NCBI]
|
3.04658e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
3.03012e-05
|
|
|
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
[NCBI]
|
3.03012e-05
|
|
|
cirrhosis, familial
|
[NCBI]
|
2.94062e-05
|
|
|
LCAT
|
[NCBI]
|
2.86004e-05
|
|
|
STARD3
|
[NCBI]
|
2.85028e-05
|
|
|
FBS
|
[NCBI]
|
2.77699e-05
|
|
|
PC
|
[NCBI]
|
2.76952e-05
|
|
|
ABCB11
|
[NCBI]
|
2.7022e-05
|
|
|
hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
|
[NCBI]
|
2.70181e-05
|
|
|
CJD
|
[NCBI]
|
2.68888e-05
|
|
|
glycogen storage disease vi
|
[NCBI]
|
2.68769e-05
|
|
|
ORW2
|
[NCBI]
|
2.6305e-05
|
|
|
PLG
|
[NCBI]
|
2.59063e-05
|
|
|
SLSN1
|
[NCBI]
|
2.56271e-05
|
|
|
BCS1L
|
[NCBI]
|
2.54906e-05
|
|
|
SLC10A2
|
[NCBI]
|
2.54906e-05
|
|
|
FED
|
[NCBI]
|
2.49812e-05
|
|
|
acyl-coa dehydrogenase, medium-chain, deficiency of
|
[NCBI]
|
2.49812e-05
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
2.43647e-05
|
|
|
KRT8
|
[NCBI]
|
2.42834e-05
|
|
|
CYP2A6
|
[NCBI]
|
2.42834e-05
|
|
|
HSD17B4
|
[NCBI]
|
2.42834e-05
|
|
|
GFAP
|
[NCBI]
|
2.35682e-05
|
|
|
RELA
|
[NCBI]
|
2.32152e-05
|
|
|
GSK3B
|
[NCBI]
|
2.32152e-05
|
|
|
ALMS
|
[NCBI]
|
2.32107e-05
|
|
|
refsum disease, infantile form
|
[NCBI]
|
2.32107e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
2.27475e-05
|
|
|
lecithin:cholesterol acyltransferase deficiency
|
[NCBI]
|
2.26693e-05
|
|
|
citrullinemia, classic
|
[NCBI]
|
2.16495e-05
|
|
|
NPHP1
|
[NCBI]
|
2.16495e-05
|
|
|
hepatocellular carcinoma
|
[NCBI]
|
2.11682e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
2.07043e-05
|
|
|
IGFALS
|
[NCBI]
|
2.04219e-05
|
|
|
FLT1
|
[NCBI]
|
1.98743e-05
|
|
|
CFTR
|
[NCBI]
|
1.97204e-05
|
|
|
TGD
|
[NCBI]
|
1.94069e-05
|
|
|
HADHA
|
[NCBI]
|
1.92023e-05
|
|
|
RCDP1
|
[NCBI]
|
1.86116e-05
|
|
|
LYZ
|
[NCBI]
|
1.85777e-05
|
|
|
GSTM1
|
[NCBI]
|
1.85777e-05
|
|
|
PKHD1
|
[NCBI]
|
1.85777e-05
|
|
|
HIGM1
|
[NCBI]
|
1.82326e-05
|
|
|
CCK
|
[NCBI]
|
1.79282e-05
|
|
|
DKC
|
[NCBI]
|
1.75085e-05
|
|
|
GNMT
|
[NCBI]
|
1.74482e-05
|
|
|
TG
|
[NCBI]
|
1.66845e-05
|
|
|
PF4
|
[NCBI]
|
1.66607e-05
|
|
|
RBP4
|
[NCBI]
|
1.59909e-05
|
|
|
AACT
|
[NCBI]
|
1.5556e-05
|
|
|
DJS
|
[NCBI]
|
1.49919e-05
|
|
|
BCHE
|
[NCBI]
|
1.47556e-05
|
|
|
PEMT
|
[NCBI]
|
1.4749e-05
|
|
|
ACADS
|
[NCBI]
|
1.4749e-05
|
|
|
VIP
|
[NCBI]
|
1.38776e-05
|
|
|
galactosemia
|
[NCBI]
|
1.36652e-05
|
|
|
LRP1
|
[NCBI]
|
1.35663e-05
|
|
|
CSF2
|
[NCBI]
|
1.33408e-05
|
|
|
IL6
|
[NCBI]
|
1.31952e-05
|
|
|
CYBB
|
[NCBI]
|
1.30244e-05
|
|
|
XDH
|
[NCBI]
|
1.28575e-05
|
|
|
NAT1
|
[NCBI]
|
1.24274e-05
|
|
|
IL18
|
[NCBI]
|
1.24274e-05
|
|
|
ATF3
|
[NCBI]
|
1.24274e-05
|
|
|
HRG
|
[NCBI]
|
1.21453e-05
|
|
|
THPO
|
[NCBI]
|
1.21453e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
1.20504e-05
|
|
|
ABL
|
[NCBI]
|
1.18393e-05
|
|
|
CEACAM1
|
[NCBI]
|
1.16106e-05
|
|
|
PROCR
|
[NCBI]
|
1.11114e-05
|
|
|
SLE
|
[NCBI]
|
1.07971e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
1.06439e-05
|
|
|
POLG
|
[NCBI]
|
1.04209e-05
|
|
|
F2R
|
[NCBI]
|
1.04209e-05
|
|
|
coproporphyria
|
[NCBI]
|
1.04209e-05
|
|
|
TYMS
|
[NCBI]
|
1.02875e-05
|
|
|
ATP7B
|
[NCBI]
|
9.99472e-06
|
|
|
LPL
|
[NCBI]
|
9.67034e-06
|
|
|
VDR
|
[NCBI]
|
9.41391e-06
|
|
|
HP
|
[NCBI]
|
9.21314e-06
|
|
|
AMACR
|
[NCBI]
|
8.51191e-06
|
|
|
MUC1
|
[NCBI]
|
8.40458e-06
|
|
|
CGD
|
[NCBI]
|
8.11321e-06
|
|
|
APOA1
|
[NCBI]
|
8.03123e-06
|
|
|
LIPC
|
[NCBI]
|
7.72978e-06
|
|
|
PKD2
|
[NCBI]
|
7.44224e-06
|
|
|
CRH
|
[NCBI]
|
7.40684e-06
|
|
|
glycogen storage disease ii
|
[NCBI]
|
6.96738e-06
|
|
|
TNFSF11
|
[NCBI]
|
6.77799e-06
|
|
|
COMT
|
[NCBI]
|
6.37424e-06
|
|
|
PTGS2
|
[NCBI]
|
6.29617e-06
|
|
|
LBP
|
[NCBI]
|
6.18189e-06
|
|
|
HD
|
[NCBI]
|
6.11453e-06
|
|
|
NR1I2
|
[NCBI]
|
6.06992e-06
|
|
|
FA
|
[NCBI]
|
5.91285e-06
|
|
|
ASS
|
[NCBI]
|
5.74725e-06
|
|
|
APS1
|
[NCBI]
|
5.67995e-06
|
|
|
ALPS
|
[NCBI]
|
5.48807e-06
|
|
|
TFPI
|
[NCBI]
|
5.24632e-06
|
|
|
factor v deficiency
|
[NCBI]
|
5.06389e-06
|
|
|
NGFR
|
[NCBI]
|
5.06389e-06
|
|
|
MBL2
|
[NCBI]
|
4.59024e-06
|
|
|
MAS
|
[NCBI]
|
4.22103e-06
|
|
|
ABCB1
|
[NCBI]
|
4.00628e-06
|
|
|
NPPA
|
[NCBI]
|
3.38156e-06
|
|
|
IP
|
[NCBI]
|
3.14732e-06
|
|
|
CVID
|
[NCBI]
|
3.08251e-06
|
|
|
ADA
|
[NCBI]
|
2.4409e-06
|
|
|
AHR
|
[NCBI]
|
2.34603e-06
|
|
|
EIG
|
[NCBI]
|
2.20529e-06
|
|
|
AGER
|
[NCBI]
|
1.84262e-06
|
|
|
PPARA
|
[NCBI]
|
1.41137e-06
|
|
|
APOB
|
[NCBI]
|
1.32403e-06
|
|
|
F3
|
[NCBI]
|
1.25738e-06
|
|
|
G6PD
|
[NCBI]
|
1.10175e-06
|
|
|
ACP5
|
[NCBI]
|
9.58386e-07
|
|
|
ALD
|
[NCBI]
|
9.51412e-07
|
|
|
CD
|
[NCBI]
|
9.29875e-07
|
|
|
OSM
|
[NCBI]
|
8.55997e-07
|
|
|
TF
|
[NCBI]
|
8.43941e-07
|
|
|
SOD2
|
[NCBI]
|
8.31571e-07
|
|
|
GJA1
|
[NCBI]
|
7.92387e-07
|
|
|
TLR4
|
[NCBI]
|
5.88644e-07
|
|
|
CTGF
|
[NCBI]
|
5.67262e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
5.6626e-07
|
|
|
SHBG
|
[NCBI]
|
3.83417e-07
|
|
|
TNFRSF11B
|
[NCBI]
|
3.50467e-07
|
|
|
SPP1
|
[NCBI]
|
3.37655e-07
|
|
|
FMF
|
[NCBI]
|
3.28952e-07
|
|
|
PXE
|
[NCBI]
|
2.34487e-07
|
|
|
GIST
|
[NCBI]
|
1.75665e-07
|
|
|
BWS
|
[NCBI]
|
1.67793e-07
|
|
|
TTR
|
[NCBI]
|
1.53454e-07
|
|
|
FGF7
|
[NCBI]
|
9.18493e-08
|
|
|
IL2
|
[NCBI]
|
8.80398e-08
|
|
|
CP
|
[NCBI]
|
8.61687e-08
|
|
|
ACE
|
[NCBI]
|
2.51255e-08
|
|