|
OMIM |
Link |
Information gain |
01 |
|
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism
|
[NCBI]
|
0.00274276
|
|
|
gastroschisis
|
[NCBI]
|
0.00167158
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.000844839
|
|
|
THAS
|
[NCBI]
|
0.000844839
|
|
|
omphalocele
|
[NCBI]
|
0.000720524
|
|
|
DHS
|
[NCBI]
|
0.000660767
|
|
|
ATD1
|
[NCBI]
|
0.000562717
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000372919
|
|
|
FSHMD1A
|
[NCBI]
|
0.000355547
|
|
|
prune belly syndrome with pulmonic stenosis, mental retardation, and deafness
|
[NCBI]
|
0.000205935
|
|
|
AFP
|
[NCBI]
|
0.000170524
|
|
|
paine syndrome
|
[NCBI]
|
0.000166678
|
|
|
desmoid disease, hereditary
|
[NCBI]
|
0.000166678
|
|
|
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema
|
[NCBI]
|
0.000151872
|
|
|
carnevale syndrome
|
[NCBI]
|
0.000151872
|
|
|
glycogen storage disease 0, liver
|
[NCBI]
|
0.000135125
|
|
|
ACHE
|
[NCBI]
|
0.000117292
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
0.000114006
|
|
|
HSAN1
|
[NCBI]
|
9.84925e-05
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
7.42046e-05
|
|
|
DFSP
|
[NCBI]
|
4.74095e-05
|
|
|
GYS2
|
[NCBI]
|
4.48515e-05
|
|
|
AEBP1
|
[NCBI]
|
3.95374e-05
|
|
|
BWS
|
[NCBI]
|
3.04857e-05
|
|
|
MEN1
|
[NCBI]
|
2.66337e-05
|
|
|
apc gene
|
[NCBI]
|
2.54979e-05
|
|
|
PD
|
[NCBI]
|
1.28608e-05
|
|
|
APC
|
[NCBI]
|
1.22077e-05
|
|
|
XDH
|
[NCBI]
|
1.12989e-05
|
|
|
KLK3
|
[NCBI]
|
5.74078e-06
|
|
|
HGF
|
[NCBI]
|
3.6556e-06
|
|
|
MPO
|
[NCBI]
|
3.27816e-06
|
|
|
VEGF
|
[NCBI]
|
2.44049e-06
|
|
|
CF
|
[NCBI]
|
1.57204e-06
|
|
|
PTH
|
[NCBI]
|
1.34678e-06
|
|
|
PRL
|
[NCBI]
|
9.73328e-07
|
|
|
NPY
|
[NCBI]
|
9.19928e-07
|
|
|
EGF
|
[NCBI]
|
3.98384e-07
|
|