|
OMIM |
Link |
Information
gain |
01 |
|
|
spiegler-brooke syndrome
|
[NCBI]
|
0.00143026
|
|
|
|
schimmelpenning-feuerstein-mims syndrome
|
[NCBI]
|
0.00131477
|
|
|
|
hemangioma, capillary infantile
|
[NCBI]
|
0.000673834
|
|
|
|
nevi flammei, familial multiple
|
[NCBI]
|
0.000647644
|
|
|
|
trichoepithelioma, multiple familial
|
[NCBI]
|
0.000647644
|
|
|
|
MTS
|
[NCBI]
|
0.000596588
|
|
|
|
BZX
|
[NCBI]
|
0.000558521
|
|
|
|
phace association
|
[NCBI]
|
0.000532186
|
|
|
|
hemangiomas, cavernous, of face and supraumbilical midline raphe
|
[NCBI]
|
0.000315118
|
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000273386
|
|
|
|
TS
|
[NCBI]
|
0.00016309
|
|
|
|
fibromatosis, juvenile hyaline
|
[NCBI]
|
0.000155683
|
|
|
|
CD
|
[NCBI]
|
0.000144378
|
|
|
|
BCNS
|
[NCBI]
|
0.000126146
|
|
|
|
dermoid cysts, familial frontonasal
|
[NCBI]
|
0.000122855
|
|
|
|
CCM
|
[NCBI]
|
0.000105491
|
|
|
|
aortic arch interruption, facial palsy, and retinal coloboma
|
[NCBI]
|
0.00010039
|
|
|
|
sebaceous nevus syndrome and hemimegalencephaly
|
[NCBI]
|
0.00010039
|
|
|
|
syringomas, multiple
|
[NCBI]
|
9.19162e-05
|
|
|
|
sturge-weber syndrome
|
[NCBI]
|
6.8615e-05
|
|
|
|
sc phocomelia syndrome
|
[NCBI]
|
6.8615e-05
|
|
|
|
NF1
|
[NCBI]
|
6.44983e-05
|
|
|
|
GVM
|
[NCBI]
|
6.23392e-05
|
|
|
|
CEACAM5
|
[NCBI]
|
6.18037e-05
|
|
|
|
DFSP
|
[NCBI]
|
6.11232e-05
|
|
|
|
CYLD
|
[NCBI]
|
6.03876e-05
|
|
|
|
PHOX2B
|
[NCBI]
|
5.33506e-05
|
|
|
|
BWS
|
[NCBI]
|
5.22323e-05
|
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
4.83906e-05
|
|
|
|
MSH2
|
[NCBI]
|
4.33956e-05
|
|
|
|
costello syndrome
|
[NCBI]
|
4.25659e-05
|
|
|
|
CCL17
|
[NCBI]
|
4.113e-05
|
|
|
|
MEN1
|
[NCBI]
|
3.48126e-05
|
|
|
|
ALK
|
[NCBI]
|
2.92554e-05
|
|
|
|
RB1
|
[NCBI]
|
2.8548e-05
|
|
|
|
EV
|
[NCBI]
|
2.63003e-05
|
|
|
|
LAM
|
[NCBI]
|
2.34146e-05
|
|
|
|
MUC1
|
[NCBI]
|
1.723e-05
|
|
|
|
GFAP
|
[NCBI]
|
7.90976e-06
|
|
|
|
APC
|
[NCBI]
|
1.80844e-06
|
|
