|
OMIM |
Link |
Information gain |
01 |
|
lymphedema, microcephaly, chorioretinopathy syndrome
|
[NCBI]
|
0.00999221
|
|
|
hennekam lymphangiectasia-lymphedema syndrome
|
[NCBI]
|
0.00486634
|
|
|
cholestasis-lymphedema syndrome
|
[NCBI]
|
0.00420327
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
0.00197776
|
|
|
lymphedema, hereditary, i
|
[NCBI]
|
0.00154098
|
|
|
CPL
|
[NCBI]
|
0.00130508
|
|
|
lymphedema, hereditary, ii
|
[NCBI]
|
0.00118119
|
|
|
FLT4
|
[NCBI]
|
0.000676537
|
|
|
mullerian derivatives, persistence of, with lymphangiectasia and postaxial polydactyly
|
[NCBI]
|
0.000614201
|
|
|
FOXC2
|
[NCBI]
|
0.000551933
|
|
|
yellow nail syndrome
|
[NCBI]
|
0.000428757
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000415623
|
|
|
lymphedema and ptosis
|
[NCBI]
|
0.000234146
|
|
|
NS1
|
[NCBI]
|
0.00013526
|
|
|
lymphedema, atrial septal defect, and facial changes
|
[NCBI]
|
0.000116948
|
|
|
lymphedema and cerebral arteriovenous anomaly
|
[NCBI]
|
0.000116948
|
|
|
hypotrichosis-lymphedema-telangiectasia syndrome
|
[NCBI]
|
0.000116948
|
|
|
lymphedema, congenital recessive
|
[NCBI]
|
0.000116948
|
|
|
lymphedema-hypoparathyroidism syndrome
|
[NCBI]
|
0.000116948
|
|
|
hydrops fetalis, idiopathic
|
[NCBI]
|
8.60172e-05
|
|
|
LIS2
|
[NCBI]
|
8.05207e-05
|
|
|
chorioretinal dysplasia-microcephaly-mental retardation syndrome
|
[NCBI]
|
7.31844e-05
|
|
|
kanzaki disease
|
[NCBI]
|
7.04818e-05
|
|
|
PDPN
|
[NCBI]
|
7.00756e-05
|
|
|
SOX18
|
[NCBI]
|
7.00756e-05
|
|
|
IP
|
[NCBI]
|
6.6499e-05
|
|
|
VEGFC
|
[NCBI]
|
6.48763e-05
|
|
|
NAGA
|
[NCBI]
|
5.39062e-05
|
|
|
VEGF
|
[NCBI]
|
5.09867e-05
|
|
|
RELN
|
[NCBI]
|
4.88341e-05
|
|
|
SPG7
|
[NCBI]
|
4.54987e-05
|
|
|
PEPD
|
[NCBI]
|
4.39318e-05
|
|
|
CF
|
[NCBI]
|
3.69138e-05
|
|
|
sotos syndrome
|
[NCBI]
|
3.62816e-05
|
|
|
aortic valve disease
|
[NCBI]
|
3.54637e-05
|
|
|
RNASE2
|
[NCBI]
|
3.3097e-05
|
|
|
KDR
|
[NCBI]
|
2.78257e-05
|
|
|
RA
|
[NCBI]
|
2.05804e-05
|
|
|
HGF
|
[NCBI]
|
4.29859e-06
|
|
|
AD
|
[NCBI]
|
3.29349e-06
|
|