|
OMIM |
Link |
Information gain |
01 |
|
hemangioma, capillary infantile
|
[NCBI]
|
0.00408847
|
|
|
angioma, hereditary neurocutaneous
|
[NCBI]
|
0.00408847
|
|
|
blue rubber bleb nevus
|
[NCBI]
|
0.00315494
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.002176
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
0.00181078
|
|
|
nevus flammeus of nape of neck
|
[NCBI]
|
0.00135446
|
|
|
nevi flammei, familial multiple
|
[NCBI]
|
0.00113349
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000892809
|
|
|
angioma serpiginosum, x-linked
|
[NCBI]
|
0.00067472
|
|
|
phace association
|
[NCBI]
|
0.000603463
|
|
|
BRRS
|
[NCBI]
|
0.000522197
|
|
|
proteus syndrome
|
[NCBI]
|
0.000512203
|
|
|
VHL
|
[NCBI]
|
0.000418984
|
|
|
hemangiomas, cavernous, of face and supraumbilical midline raphe
|
[NCBI]
|
0.000282804
|
|
|
VEGF
|
[NCBI]
|
0.000241316
|
|
|
vascular malformation, primary intraosseous
|
[NCBI]
|
0.000224694
|
|
|
angioma, tufted
|
[NCBI]
|
0.000224694
|
|
|
FRNS
|
[NCBI]
|
0.000218277
|
|
|
enchondromatosis, multiple
|
[NCBI]
|
0.000209119
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
0.000200419
|
|
|
aortic aneurysm, giant congenital
|
[NCBI]
|
0.000193755
|
|
|
TS
|
[NCBI]
|
0.000193586
|
|
|
RA
|
[NCBI]
|
0.000183169
|
|
|
CCM
|
[NCBI]
|
0.000146783
|
|
|
megalencephaly-cutis marmorata telangiectatica congenita
|
[NCBI]
|
0.000140288
|
|
|
SLE
|
[NCBI]
|
0.000126406
|
|
|
HHT
|
[NCBI]
|
0.000124396
|
|
|
CD
|
[NCBI]
|
0.000112921
|
|
|
hemangiomas of small intestine
|
[NCBI]
|
0.000112254
|
|
|
hemangiomatosis, familial pulmonary capillary
|
[NCBI]
|
0.000112254
|
|
|
chemodectoma, intraabdominal, with cutaneous angiolipomas
|
[NCBI]
|
0.000112254
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
9.57622e-05
|
|
|
HFM
|
[NCBI]
|
8.91667e-05
|
|
|
nevus, keratinocytic, nonepidermolytic
|
[NCBI]
|
8.13307e-05
|
|
|
macrocephaly
|
[NCBI]
|
8.13307e-05
|
|
|
DIO3
|
[NCBI]
|
7.82236e-05
|
|
|
myelofibrosis, familial
|
[NCBI]
|
7.58383e-05
|
|
|
angiolipomatosis, familial
|
[NCBI]
|
7.58383e-05
|
|
|
PKDTS
|
[NCBI]
|
7.58383e-05
|
|
|
angioma serpiginosum, autosomal dominant
|
[NCBI]
|
7.17582e-05
|
|
|
MUC1
|
[NCBI]
|
6.89891e-05
|
|
|
WT1
|
[NCBI]
|
6.79337e-05
|
|
|
VHL
|
[NCBI]
|
6.44479e-05
|
|
|
KDR
|
[NCBI]
|
5.8385e-05
|
|
|
sc phocomelia syndrome
|
[NCBI]
|
5.80907e-05
|
|
|
noonan-like/multiple giant cell lesion syndrome
|
[NCBI]
|
5.80907e-05
|
|
|
wagr syndrome
|
[NCBI]
|
5.66309e-05
|
|
|
GVM
|
[NCBI]
|
5.18533e-05
|
|
|
IFNA2
|
[NCBI]
|
5.1369e-05
|
|
|
mulibrey nanism
|
[NCBI]
|
4.9917e-05
|
|
|
ATF1
|
[NCBI]
|
4.7045e-05
|
|
|
long-chain 3-hydroxyacyl-coa dehydrogenase deficiency
|
[NCBI]
|
4.59215e-05
|
|
|
FLT4
|
[NCBI]
|
4.24615e-05
|
|
|
pheochromocytoma
|
[NCBI]
|
4.01184e-05
|
|
|
FUS
|
[NCBI]
|
3.9896e-05
|
|
|
PHOX2B
|
[NCBI]
|
3.93472e-05
|
|
|
SKP2
|
[NCBI]
|
3.69874e-05
|
|
|
PGL1
|
[NCBI]
|
3.55668e-05
|
|
|
FGF1
|
[NCBI]
|
3.54398e-05
|
|
|
IRS1
|
[NCBI]
|
3.32117e-05
|
|
|
TSC1
|
[NCBI]
|
3.11686e-05
|
|
|
HMI
|
[NCBI]
|
3.05019e-05
|
|
|
COL3A1
|
[NCBI]
|
2.96793e-05
|
|
|
MTS
|
[NCBI]
|
2.9051e-05
|
|
|
VIM
|
[NCBI]
|
2.52046e-05
|
|
|
PTEN
|
[NCBI]
|
2.0063e-05
|
|
|
GFAP
|
[NCBI]
|
1.69771e-05
|
|
|
STAT3
|
[NCBI]
|
1.54322e-05
|
|
|
FRAP1
|
[NCBI]
|
1.04339e-05
|
|
|
TFPI
|
[NCBI]
|
1.02203e-05
|
|
|
PTHLH
|
[NCBI]
|
8.31854e-06
|
|
|
BWS
|
[NCBI]
|
7.80356e-06
|
|
|
TNF
|
[NCBI]
|
6.89297e-06
|
|
|
CEACAM5
|
[NCBI]
|
5.3257e-06
|
|
|
F3
|
[NCBI]
|
3.29391e-06
|
|
|
PTH
|
[NCBI]
|
9.17989e-07
|
|
|
AR
|
[NCBI]
|
6.04156e-07
|
|
|
EGFR
|
[NCBI]
|
3.77823e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
2.944e-07
|
|
|
AFP
|
[NCBI]
|
5.3972e-08
|
|
|
PCNA
|
[NCBI]
|
1.53558e-09
|
|