|
OMIM |
Link |
Information gain |
01 |
|
NLS
|
[NCBI]
|
0.00210699
|
|
|
peho syndrome
|
[NCBI]
|
0.00125516
|
|
|
MPO
|
[NCBI]
|
0.00110499
|
|
|
cornea guttata with anterior polar cataracts
|
[NCBI]
|
0.000952205
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.000676489
|
|
|
myopathy, autophagic vacuolar, infantile-onset
|
[NCBI]
|
0.000599634
|
|
|
melkersson-rosenthal syndrome
|
[NCBI]
|
0.000560268
|
|
|
macular edema, cystoid
|
[NCBI]
|
0.000560268
|
|
|
cholestasis-lymphedema syndrome
|
[NCBI]
|
0.000528971
|
|
|
lethal congenital contracture syndrome 1
|
[NCBI]
|
0.000528971
|
|
|
CHED1
|
[NCBI]
|
0.000503004
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000487141
|
|
|
short rib-polydactyly syndrome, type iv
|
[NCBI]
|
0.000402241
|
|
|
DHS
|
[NCBI]
|
0.000327324
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000268462
|
|
|
RA
|
[NCBI]
|
0.000260339
|
|
|
nevo syndrome
|
[NCBI]
|
0.000168044
|
|
|
VEGF
|
[NCBI]
|
0.000161327
|
|
|
CRH
|
[NCBI]
|
0.00013191
|
|
|
lymphedema, hereditary, i
|
[NCBI]
|
0.000122718
|
|
|
HBZ
|
[NCBI]
|
0.000121049
|
|
|
tight skin contracture syndrome, lethal
|
[NCBI]
|
0.000113465
|
|
|
NPPA
|
[NCBI]
|
0.000107763
|
|
|
edema, familial idiopathic, prepubertal
|
[NCBI]
|
0.000106407
|
|
|
COXPD5
|
[NCBI]
|
0.000106407
|
|
|
distichiasis with congenital anomalies of the heart and peripheral vasculature
|
[NCBI]
|
0.000106407
|
|
|
aplasia cutis congenita with intestinal lymphangiectasia
|
[NCBI]
|
0.000106407
|
|
|
pancreatic insufficiency, combined exocrine
|
[NCBI]
|
0.000106407
|
|
|
enteropathy, familial, with villous edema and immunoglobulin g2 deficiency
|
[NCBI]
|
0.000106407
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
0.000104753
|
|
|
NPHS1
|
[NCBI]
|
0.000101846
|
|
|
AQP1
|
[NCBI]
|
8.94518e-05
|
|
|
pulmonary hypertension, primary, autosomal recessive
|
[NCBI]
|
7.54979e-05
|
|
|
hydrops fetalis, idiopathic
|
[NCBI]
|
7.54979e-05
|
|
|
fetal akinesia syndrome, x-linked
|
[NCBI]
|
7.54979e-05
|
|
|
acrocephalopolydactylous dysplasia
|
[NCBI]
|
7.54979e-05
|
|
|
fountain syndrome
|
[NCBI]
|
7.54979e-05
|
|
|
HAE
|
[NCBI]
|
7.21096e-05
|
|
|
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema
|
[NCBI]
|
7.00124e-05
|
|
|
AHR
|
[NCBI]
|
6.94786e-05
|
|
|
membranoproliferative glomerulonephritis, x-linked
|
[NCBI]
|
6.59392e-05
|
|
|
yellow nail syndrome
|
[NCBI]
|
6.59392e-05
|
|
|
GPRK6
|
[NCBI]
|
6.35238e-05
|
|
|
anemia, autoimmune hemolytic
|
[NCBI]
|
6.26979e-05
|
|
|
enterokinase deficiency
|
[NCBI]
|
6.00063e-05
|
|
|
schneckenbecken dysplasia
|
[NCBI]
|
6.00063e-05
|
|
|
CHED2
|
[NCBI]
|
5.77053e-05
|
|
|
hydrops-ectopic calcification-moth-eaten skeletal dysplasia
|
[NCBI]
|
5.39144e-05
|
|
|
AVP
|
[NCBI]
|
5.26797e-05
|
|
|
CXCL6
|
[NCBI]
|
4.97597e-05
|
|
|
SLC35D1
|
[NCBI]
|
4.97597e-05
|
|
|
MTF1
|
[NCBI]
|
4.97597e-05
|
|
|
OCLN
|
[NCBI]
|
4.97597e-05
|
|
|
TIE1
|
[NCBI]
|
4.97597e-05
|
|
|
multiple pterygium syndrome, lethal type
|
[NCBI]
|
4.95308e-05
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
4.71693e-05
|
|
|
SFD
|
[NCBI]
|
4.71693e-05
|
|
|
CF
|
[NCBI]
|
4.63886e-05
|
|
|
ehlers-danlos syndrome, type vii, autosomal recessive
|
[NCBI]
|
4.61105e-05
|
|
|
autoimmune disease
|
[NCBI]
|
4.51195e-05
|
|
|
MRPS22
|
[NCBI]
|
4.45749e-05
|
|
|
factor xii deficiency
|
[NCBI]
|
4.41882e-05
|
|
|
PPCD1
|
[NCBI]
|
4.41882e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
4.41882e-05
|
|
|
heart block, congenital
|
[NCBI]
|
4.33099e-05
|
|
|
LPG
|
[NCBI]
|
4.33099e-05
|
|
|
CRHR2
|
[NCBI]
|
4.12137e-05
|
|
|
JBS
|
[NCBI]
|
3.95451e-05
|
|
|
CEACAM5
|
[NCBI]
|
3.9539e-05
|
|
|
STGD1
|
[NCBI]
|
3.65315e-05
|
|
|
CGL2
|
[NCBI]
|
3.65315e-05
|
|
|
citrullinemia, classic
|
[NCBI]
|
3.59952e-05
|
|
|
ANGPT1
|
[NCBI]
|
3.50858e-05
|
|
|
mucopolysaccharidosis type vii
|
[NCBI]
|
3.44935e-05
|
|
|
AQP5
|
[NCBI]
|
3.36775e-05
|
|
|
F2RL1
|
[NCBI]
|
3.36775e-05
|
|
|
FCAS
|
[NCBI]
|
3.31305e-05
|
|
|
FIH
|
[NCBI]
|
3.27029e-05
|
|
|
ANGPT2
|
[NCBI]
|
3.03791e-05
|
|
|
NPHS1
|
[NCBI]
|
2.86781e-05
|
|
|
CTSB
|
[NCBI]
|
2.79293e-05
|
|
|
sotos syndrome
|
[NCBI]
|
2.63424e-05
|
|
|
IGKC
|
[NCBI]
|
2.59837e-05
|
|
|
TACR1
|
[NCBI]
|
2.54153e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
2.53054e-05
|
|
|
FOXC2
|
[NCBI]
|
2.48794e-05
|
|
|
KLK3
|
[NCBI]
|
2.44954e-05
|
|
|
NMU
|
[NCBI]
|
2.38921e-05
|
|
|
GALP
|
[NCBI]
|
2.34352e-05
|
|
|
LSA
|
[NCBI]
|
2.32272e-05
|
|
|
PAM
|
[NCBI]
|
2.29998e-05
|
|
|
PRSS1
|
[NCBI]
|
2.25842e-05
|
|
|
PMM2
|
[NCBI]
|
2.21865e-05
|
|
|
IL8
|
[NCBI]
|
2.18054e-05
|
|
|
GPI
|
[NCBI]
|
2.11929e-05
|
|
|
CGD
|
[NCBI]
|
2.05318e-05
|
|
|
AVSD
|
[NCBI]
|
2.01891e-05
|
|
|
PYY
|
[NCBI]
|
1.9204e-05
|
|
|
NS1
|
[NCBI]
|
1.81658e-05
|
|
|
NGFB
|
[NCBI]
|
1.71582e-05
|
|
|
AFP
|
[NCBI]
|
1.5659e-05
|
|
|
CCL2
|
[NCBI]
|
1.4738e-05
|
|
|
MAP3K5
|
[NCBI]
|
1.39487e-05
|
|
|
RNASE2
|
[NCBI]
|
1.36534e-05
|
|
|
PTGS2
|
[NCBI]
|
1.32299e-05
|
|
|
VIP
|
[NCBI]
|
1.27679e-05
|
|
|
TNF
|
[NCBI]
|
1.20724e-05
|
|
|
SRC
|
[NCBI]
|
1.18479e-05
|
|
|
PPARG
|
[NCBI]
|
1.098e-05
|
|
|
GUSB
|
[NCBI]
|
1.02039e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
1.0007e-05
|
|
|
ALB
|
[NCBI]
|
9.43773e-06
|
|
|
SOD2
|
[NCBI]
|
9.32836e-06
|
|
|
PRL
|
[NCBI]
|
9.16944e-06
|
|
|
EGF
|
[NCBI]
|
8.58391e-06
|
|
|
PCNA
|
[NCBI]
|
8.49788e-06
|
|
|
MBP
|
[NCBI]
|
8.25502e-06
|
|
|
XDH
|
[NCBI]
|
8.2368e-06
|
|
|
HDC
|
[NCBI]
|
7.56752e-06
|
|
|
PXE
|
[NCBI]
|
7.30177e-06
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
7.06661e-06
|
|
|
HGF
|
[NCBI]
|
6.2658e-06
|
|
|
ADM
|
[NCBI]
|
5.85935e-06
|
|
|
OSM
|
[NCBI]
|
5.59005e-06
|
|
|
PMP22
|
[NCBI]
|
5.46043e-06
|
|
|
GJA1
|
[NCBI]
|
5.46043e-06
|
|
|
GFAP
|
[NCBI]
|
4.51208e-06
|
|
|
PPARA
|
[NCBI]
|
4.50887e-06
|
|
|
BWS
|
[NCBI]
|
4.13674e-06
|
|
|
GIST
|
[NCBI]
|
4.10815e-06
|
|
|
ACHE
|
[NCBI]
|
3.92902e-06
|
|
|
PD
|
[NCBI]
|
3.63461e-06
|
|
|
STAT3
|
[NCBI]
|
3.58335e-06
|
|
|
GHRH
|
[NCBI]
|
3.55526e-06
|
|
|
CP
|
[NCBI]
|
3.49967e-06
|
|
|
CCK
|
[NCBI]
|
3.13913e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.91866e-06
|
|
|
GIP
|
[NCBI]
|
2.60052e-06
|
|
|
CAT
|
[NCBI]
|
2.53653e-06
|
|
|
CFTR
|
[NCBI]
|
2.38828e-06
|
|
|
IL2
|
[NCBI]
|
2.00426e-06
|
|
|
CNTF
|
[NCBI]
|
1.39788e-06
|
|
|
GNRH1
|
[NCBI]
|
1.30765e-06
|
|
|
temporal arteritis
|
[NCBI]
|
1.2477e-06
|
|
|
TLR4
|
[NCBI]
|
1.11704e-06
|
|
|
SLE
|
[NCBI]
|
8.25987e-07
|
|
|
NPY
|
[NCBI]
|
8.10432e-07
|
|
|
ACP5
|
[NCBI]
|
8.03665e-07
|
|
|
RNASE3
|
[NCBI]
|
7.51602e-07
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
1.20549e-07
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.06551e-07
|
|
|
FMF
|
[NCBI]
|
1.05802e-07
|
|
|
CD
|
[NCBI]
|
1.99677e-08
|
|
|
SPP1
|
[NCBI]
|
5.64176e-09
|
|