|
OMIM |
Link |
Information gain |
01 |
|
ATD1
|
[NCBI]
|
0.00291706
|
|
|
adducted thumbs syndrome
|
[NCBI]
|
0.000714407
|
|
|
spondylometaphyseal dysplasia, sedaghatian type
|
[NCBI]
|
0.000621736
|
|
|
pierre robin sequence with pectus excavatum and rib and scapular anomalies
|
[NCBI]
|
0.000590318
|
|
|
FSHMD1A
|
[NCBI]
|
0.000532147
|
|
|
glycogen storage disease ii
|
[NCBI]
|
0.000492588
|
|
|
myeloproliferative syndrome, transient
|
[NCBI]
|
0.000321967
|
|
|
poland syndrome
|
[NCBI]
|
0.00031277
|
|
|
CF
|
[NCBI]
|
0.000294654
|
|
|
stuve-wiedemann syndrome
|
[NCBI]
|
0.000288302
|
|
|
HMERF
|
[NCBI]
|
0.000285163
|
|
|
RSMD1
|
[NCBI]
|
0.000228106
|
|
|
RA
|
[NCBI]
|
0.000190178
|
|
|
MG
|
[NCBI]
|
0.000156268
|
|
|
LGMD2I
|
[NCBI]
|
0.000124031
|
|
|
SLE
|
[NCBI]
|
0.000120374
|
|
|
myopathy, distal, with early respiratory failure, autosomal dominant
|
[NCBI]
|
0.000107066
|
|
|
obesity-hypoventilation syndrome
|
[NCBI]
|
0.000107066
|
|
|
SFTPB
|
[NCBI]
|
0.000101864
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
9.92378e-05
|
|
|
TTN
|
[NCBI]
|
9.1011e-05
|
|
|
SJS1
|
[NCBI]
|
8.18596e-05
|
|
|
NEM3
|
[NCBI]
|
8.11686e-05
|
|
|
IL13
|
[NCBI]
|
8.06917e-05
|
|
|
LAM
|
[NCBI]
|
7.63559e-05
|
|
|
larsen-like syndrome, lethal type
|
[NCBI]
|
7.61552e-05
|
|
|
respiratory underresponsiveness to hypoxia and hypercapnia
|
[NCBI]
|
7.61552e-05
|
|
|
sickle cell anemia
|
[NCBI]
|
7.50072e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
7.1995e-05
|
|
|
aminopterin syndrome sine aminopterin
|
[NCBI]
|
7.06687e-05
|
|
|
TLPD
|
[NCBI]
|
7.06687e-05
|
|
|
immunodeficiency with hyper-igm, type 3
|
[NCBI]
|
6.65946e-05
|
|
|
NBR1
|
[NCBI]
|
6.39235e-05
|
|
|
choreoathetosis, hypothyroidism, and neonatal respiratory distress
|
[NCBI]
|
6.33524e-05
|
|
|
creatine phosphokinase, elevated serum
|
[NCBI]
|
6.33524e-05
|
|
|
RTT
|
[NCBI]
|
6.33209e-05
|
|
|
IL11
|
[NCBI]
|
5.8726e-05
|
|
|
IL11RA
|
[NCBI]
|
5.8726e-05
|
|
|
MDC1C
|
[NCBI]
|
5.8358e-05
|
|
|
AVP
|
[NCBI]
|
5.59721e-05
|
|
|
lenz-majewski hyperostotic dwarfism
|
[NCBI]
|
5.45652e-05
|
|
|
leiomyomatosis, esophageal and vulval, with nephropathy
|
[NCBI]
|
5.29633e-05
|
|
|
SMDP1
|
[NCBI]
|
5.15095e-05
|
|
|
CSF2RB
|
[NCBI]
|
5.08467e-05
|
|
|
SEPN1
|
[NCBI]
|
4.91861e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
4.78155e-05
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
4.78155e-05
|
|
|
JMJD6
|
[NCBI]
|
4.77651e-05
|
|
|
CD40
|
[NCBI]
|
4.65233e-05
|
|
|
HSD17B4
|
[NCBI]
|
4.65233e-05
|
|
|
CFTD
|
[NCBI]
|
4.5764e-05
|
|
|
myasthenic syndrome, congenital, associated with episodic apnea
|
[NCBI]
|
4.5764e-05
|
|
|
FMD
|
[NCBI]
|
4.48317e-05
|
|
|
KSS
|
[NCBI]
|
4.47169e-05
|
|
|
NDN
|
[NCBI]
|
4.27023e-05
|
|
|
RTD
|
[NCBI]
|
4.23319e-05
|
|
|
MMP12
|
[NCBI]
|
4.19409e-05
|
|
|
NKX2-1
|
[NCBI]
|
4.12342e-05
|
|
|
GACI
|
[NCBI]
|
4.08663e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
4.01831e-05
|
|
|
HSS
|
[NCBI]
|
4.01831e-05
|
|
|
PTPRC
|
[NCBI]
|
3.88275e-05
|
|
|
NOS2A
|
[NCBI]
|
3.88275e-05
|
|
|
sudden infant death syndrome
|
[NCBI]
|
3.83009e-05
|
|
|
EDN1
|
[NCBI]
|
3.68972e-05
|
|
|
citrullinemia, classic
|
[NCBI]
|
3.66278e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
3.61093e-05
|
|
|
IL8
|
[NCBI]
|
3.56647e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
3.56081e-05
|
|
|
SCDO1
|
[NCBI]
|
3.51233e-05
|
|
|
FKRP
|
[NCBI]
|
3.4922e-05
|
|
|
SEDC
|
[NCBI]
|
3.33291e-05
|
|
|
TF
|
[NCBI]
|
3.29999e-05
|
|
|
GAA
|
[NCBI]
|
3.26953e-05
|
|
|
LIP
|
[NCBI]
|
3.17308e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
3.09932e-05
|
|
|
MMP9
|
[NCBI]
|
2.95681e-05
|
|
|
MYH7
|
[NCBI]
|
2.87802e-05
|
|
|
FCMD
|
[NCBI]
|
2.66837e-05
|
|
|
PWS
|
[NCBI]
|
2.38437e-05
|
|
|
LPI
|
[NCBI]
|
2.22087e-05
|
|
|
MAPT
|
[NCBI]
|
2.134e-05
|
|
|
MECP2
|
[NCBI]
|
1.9997e-05
|
|
|
LS
|
[NCBI]
|
1.94803e-05
|
|
|
RNASE3
|
[NCBI]
|
1.85944e-05
|
|
|
NPPA
|
[NCBI]
|
1.82509e-05
|
|
|
OSM
|
[NCBI]
|
1.7685e-05
|
|
|
ACH
|
[NCBI]
|
1.58067e-05
|
|
|
TNF
|
[NCBI]
|
1.482e-05
|
|
|
PI
|
[NCBI]
|
1.33283e-05
|
|
|
CMH
|
[NCBI]
|
1.27746e-05
|
|
|
ACHE
|
[NCBI]
|
1.21746e-05
|
|
|
NF1
|
[NCBI]
|
1.15418e-05
|
|
|
GAPDH
|
[NCBI]
|
1.14625e-05
|
|
|
PF4
|
[NCBI]
|
1.08814e-05
|
|
|
VEGF
|
[NCBI]
|
1.01565e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
7.51198e-06
|
|
|
MFS
|
[NCBI]
|
6.7503e-06
|
|
|
SHBG
|
[NCBI]
|
6.2924e-06
|
|
|
CHAT
|
[NCBI]
|
6.17363e-06
|
|
|
MUC1
|
[NCBI]
|
4.9604e-06
|
|
|
MPO
|
[NCBI]
|
4.81544e-06
|
|
|
VIP
|
[NCBI]
|
3.38994e-06
|
|
|
F3
|
[NCBI]
|
2.98017e-06
|
|
|
CFTR
|
[NCBI]
|
2.50707e-06
|
|
|
BDNF
|
[NCBI]
|
2.33239e-06
|
|
|
TH
|
[NCBI]
|
1.74239e-06
|
|
|
CEACAM5
|
[NCBI]
|
1.51923e-06
|
|
|
HGF
|
[NCBI]
|
9.82578e-07
|
|
|
GFAP
|
[NCBI]
|
7.50801e-08
|
|
|
PRL
|
[NCBI]
|
4.8319e-08
|
|
|
EPO
|
[NCBI]
|
3.52741e-08
|
|
|
AFP
|
[NCBI]
|
1.39197e-08
|
|