|
OMIM |
Link |
Information gain |
01 |
|
3-@hydroxyisobutyric aciduria
|
[NCBI]
|
0.00132272
|
|
|
neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers
|
[NCBI]
|
0.000957753
|
|
|
cutis laxa, corneal clouding, and mental retardation
|
[NCBI]
|
0.000892923
|
|
|
x inactivation, familial skewed, 2
|
[NCBI]
|
0.000844761
|
|
|
ASD1
|
[NCBI]
|
0.00077456
|
|
|
IH
|
[NCBI]
|
0.00077456
|
|
|
ST3
|
[NCBI]
|
0.0005482
|
|
|
lipomatosis, multiple
|
[NCBI]
|
0.000516265
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
0.000249916
|
|
|
peroxidase and phospholipid deficiency in eosinophils
|
[NCBI]
|
0.000199809
|
|
|
nondisjunction
|
[NCBI]
|
0.000158497
|
|
|
dohle bodies and leukemia
|
[NCBI]
|
0.000137984
|
|
|
myelocytic leukemia-like syndrome, familial, chronic
|
[NCBI]
|
0.000110231
|
|
|
acrofacial dysostosis, catania type
|
[NCBI]
|
0.000110231
|
|
|
CES
|
[NCBI]
|
0.000101728
|
|
|
MRX58
|
[NCBI]
|
9.97678e-05
|
|
|
yemenite deaf-blind hypopigmentation syndrome
|
[NCBI]
|
9.97678e-05
|
|
|
FA
|
[NCBI]
|
8.82345e-05
|
|
|
LVNC1
|
[NCBI]
|
8.79385e-05
|
|
|
POF2A
|
[NCBI]
|
8.79385e-05
|
|
|
erythroleukemia, familial
|
[NCBI]
|
8.39247e-05
|
|
|
thyrotropin deficiency, isolated
|
[NCBI]
|
8.39247e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
8.05903e-05
|
|
|
PWS
|
[NCBI]
|
7.91233e-05
|
|
|
SMS
|
[NCBI]
|
7.81349e-05
|
|
|
ODG2
|
[NCBI]
|
7.77387e-05
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
7.52482e-05
|
|
|
currarino syndrome
|
[NCBI]
|
7.52482e-05
|
|
|
ADHR
|
[NCBI]
|
7.52482e-05
|
|
|
monosomy 7 of bone marrow
|
[NCBI]
|
7.30378e-05
|
|
|
chromosome 18q deletion syndrome
|
[NCBI]
|
6.75966e-05
|
|
|
chromosome 22q13.3 deletion syndrome
|
[NCBI]
|
6.75966e-05
|
|
|
potocki-shaffer syndrome
|
[NCBI]
|
6.46624e-05
|
|
|
CF
|
[NCBI]
|
6.40777e-05
|
|
|
exostoses, multiple, type ii
|
[NCBI]
|
6.3346e-05
|
|
|
infantile spasm syndrome, x-linked
|
[NCBI]
|
6.21134e-05
|
|
|
MVA
|
[NCBI]
|
6.21134e-05
|
|
|
BGS
|
[NCBI]
|
6.09545e-05
|
|
|
OCRL
|
[NCBI]
|
5.43544e-05
|
|
|
neural tube defects
|
[NCBI]
|
5.21008e-05
|
|
|
POF1
|
[NCBI]
|
5.21008e-05
|
|
|
testicular tumors
|
[NCBI]
|
5.14055e-05
|
|
|
apert syndrome
|
[NCBI]
|
5.14055e-05
|
|
|
hypophosphatasia, infantile
|
[NCBI]
|
5.07348e-05
|
|
|
deleted in neuroblastoma 5
|
[NCBI]
|
4.91634e-05
|
|
|
meningioma, familial
|
[NCBI]
|
4.76994e-05
|
|
|
MDLS
|
[NCBI]
|
4.71472e-05
|
|
|
hypophosphatemic rickets, x-linked dominant
|
[NCBI]
|
4.50894e-05
|
|
|
RSTS
|
[NCBI]
|
4.46088e-05
|
|
|
SCS
|
[NCBI]
|
4.2803e-05
|
|
|
sotos syndrome
|
[NCBI]
|
4.2803e-05
|
|
|
down syndrome
|
[NCBI]
|
4.11598e-05
|
|
|
RERE
|
[NCBI]
|
4.09172e-05
|
|
|
CENTA2
|
[NCBI]
|
4.09172e-05
|
|
|
AN2
|
[NCBI]
|
4.07712e-05
|
|
|
RDT
|
[NCBI]
|
3.76073e-05
|
|
|
prostate cancer
|
[NCBI]
|
3.7288e-05
|
|
|
MUC1
|
[NCBI]
|
3.7164e-05
|
|
|
porphyria variegata
|
[NCBI]
|
3.66663e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
3.60658e-05
|
|
|
MKRN1
|
[NCBI]
|
3.57857e-05
|
|
|
CMT1A
|
[NCBI]
|
3.54852e-05
|
|
|
lynch syndrome i
|
[NCBI]
|
3.38513e-05
|
|
|
NS1
|
[NCBI]
|
3.25987e-05
|
|
|
TM4SF2
|
[NCBI]
|
3.12415e-05
|
|
|
MAS
|
[NCBI]
|
3.07688e-05
|
|
|
PEPB
|
[NCBI]
|
3.04974e-05
|
|
|
ARD1A
|
[NCBI]
|
3.04974e-05
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
3.03408e-05
|
|
|
BBS4
|
[NCBI]
|
2.98365e-05
|
|
|
MIRN155
|
[NCBI]
|
2.98365e-05
|
|
|
AL-A1
|
[NCBI]
|
2.8702e-05
|
|
|
MSN
|
[NCBI]
|
2.82072e-05
|
|
|
ZNF198
|
[NCBI]
|
2.82072e-05
|
|
|
IDH1
|
[NCBI]
|
2.82072e-05
|
|
|
CD14
|
[NCBI]
|
2.73268e-05
|
|
|
HEPH
|
[NCBI]
|
2.69314e-05
|
|
|
UBE1
|
[NCBI]
|
2.69314e-05
|
|
|
CCKAR
|
[NCBI]
|
2.69314e-05
|
|
|
CNR1
|
[NCBI]
|
2.65609e-05
|
|
|
DDR1
|
[NCBI]
|
2.62122e-05
|
|
|
EV
|
[NCBI]
|
2.59232e-05
|
|
|
IL9
|
[NCBI]
|
2.55713e-05
|
|
|
FRAXE
|
[NCBI]
|
2.55713e-05
|
|
|
BBS
|
[NCBI]
|
2.4986e-05
|
|
|
TK1
|
[NCBI]
|
2.42207e-05
|
|
|
BCNS
|
[NCBI]
|
2.4102e-05
|
|
|
NKX2E
|
[NCBI]
|
2.39842e-05
|
|
|
LDHB
|
[NCBI]
|
2.37568e-05
|
|
|
CDKN1B
|
[NCBI]
|
2.25516e-05
|
|
|
SKP2
|
[NCBI]
|
2.25516e-05
|
|
|
MN
|
[NCBI]
|
2.23728e-05
|
|
|
SOX10
|
[NCBI]
|
2.21993e-05
|
|
|
PPOX
|
[NCBI]
|
2.20308e-05
|
|
|
PHEX
|
[NCBI]
|
2.17077e-05
|
|
|
XPA
|
[NCBI]
|
2.15527e-05
|
|
|
SHOX
|
[NCBI]
|
2.14016e-05
|
|
|
EGR1
|
[NCBI]
|
2.09707e-05
|
|
|
CSF2
|
[NCBI]
|
2.09707e-05
|
|
|
DFSP
|
[NCBI]
|
1.92552e-05
|
|
|
DCC
|
[NCBI]
|
1.9094e-05
|
|
|
SPARC
|
[NCBI]
|
1.83436e-05
|
|
|
DGS
|
[NCBI]
|
1.8167e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
1.81181e-05
|
|
|
IL3
|
[NCBI]
|
1.76021e-05
|
|
|
PAX6
|
[NCBI]
|
1.75253e-05
|
|
|
CPI
|
[NCBI]
|
1.65561e-05
|
|
|
COL2A1
|
[NCBI]
|
1.63573e-05
|
|
|
GCK
|
[NCBI]
|
1.62344e-05
|
|
|
FGF1
|
[NCBI]
|
1.6174e-05
|
|
|
IL4
|
[NCBI]
|
1.58242e-05
|
|
|
SRY
|
[NCBI]
|
1.57123e-05
|
|
|
KRT20
|
[NCBI]
|
1.57123e-05
|
|
|
NPM1
|
[NCBI]
|
1.47942e-05
|
|
|
HPRT1
|
[NCBI]
|
1.47942e-05
|
|
|
FGFR1
|
[NCBI]
|
1.42139e-05
|
|
|
apc gene
|
[NCBI]
|
1.27684e-05
|
|
|
DCK
|
[NCBI]
|
1.18154e-05
|
|
|
phenylketonuria
|
[NCBI]
|
1.12221e-05
|
|
|
BWS
|
[NCBI]
|
1.10871e-05
|
|
|
BCR
|
[NCBI]
|
1.08003e-05
|
|
|
APRT
|
[NCBI]
|
1.0711e-05
|
|
|
SOD1
|
[NCBI]
|
1.01653e-05
|
|
|
AS
|
[NCBI]
|
8.82705e-06
|
|
|
AD
|
[NCBI]
|
8.13124e-06
|
|
|
CAT
|
[NCBI]
|
7.71334e-06
|
|
|
HP
|
[NCBI]
|
7.31824e-06
|
|
|
AR
|
[NCBI]
|
5.17762e-06
|
|
|
FRAP1
|
[NCBI]
|
5.11733e-06
|
|
|
POMC
|
[NCBI]
|
4.85993e-06
|
|
|
CRC
|
[NCBI]
|
4.80604e-06
|
|
|
EGF
|
[NCBI]
|
4.12503e-06
|
|
|
SHH
|
[NCBI]
|
3.78754e-06
|
|
|
TYMS
|
[NCBI]
|
3.52977e-06
|
|
|
TNF
|
[NCBI]
|
3.23474e-06
|
|
|
G6PD
|
[NCBI]
|
2.68708e-06
|
|
|
F3
|
[NCBI]
|
1.81638e-06
|
|
|
AFP
|
[NCBI]
|
7.20072e-07
|
|
|
MPO
|
[NCBI]
|
6.10129e-07
|
|
|
APOE
|
[NCBI]
|
6.08173e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.47386e-07
|
|
|
EPO
|
[NCBI]
|
1.39758e-07
|
|
|
KLK3
|
[NCBI]
|
4.10453e-09
|
|
|
APC
|
[NCBI]
|
4.77738e-11
|
|