|
OMIM |
Link |
Information gain |
01 |
|
PHS
|
[NCBI]
|
0.00295011
|
|
|
renal hamartomas, nephroblastomatosis, and fetal gigantism
|
[NCBI]
|
0.00215435
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.00193559
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
0.00118764
|
|
|
basaloid follicular hamartoma syndrome, generalized, autosomal dominant
|
[NCBI]
|
0.00102539
|
|
|
PJS
|
[NCBI]
|
0.00101088
|
|
|
proteus syndrome
|
[NCBI]
|
0.00077178
|
|
|
TS
|
[NCBI]
|
0.000737225
|
|
|
comedones, familial dyskeratotic
|
[NCBI]
|
0.000672411
|
|
|
MKS2
|
[NCBI]
|
0.000601472
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
0.000461898
|
|
|
CD
|
[NCBI]
|
0.00045518
|
|
|
BRRS
|
[NCBI]
|
0.000328578
|
|
|
GLI3
|
[NCBI]
|
0.00027581
|
|
|
white sponge nevus of cannon
|
[NCBI]
|
0.000216888
|
|
|
GCPS
|
[NCBI]
|
0.000210605
|
|
|
TSC1
|
[NCBI]
|
0.000185697
|
|
|
BHD
|
[NCBI]
|
0.000177263
|
|
|
BWS
|
[NCBI]
|
0.000168594
|
|
|
MKKS
|
[NCBI]
|
0.000162034
|
|
|
SLE
|
[NCBI]
|
0.000152605
|
|
|
cleft larynx, posterior
|
[NCBI]
|
0.000152176
|
|
|
KRT4
|
[NCBI]
|
0.000139544
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
0.000123764
|
|
|
TSC2
|
[NCBI]
|
0.000115197
|
|
|
congenital heart defects, hamartomas of tongue, and polysyndactyly
|
[NCBI]
|
0.000106932
|
|
|
basal cell carcinoma, infundibulocystic
|
[NCBI]
|
8.44817e-05
|
|
|
sebaceous nevus syndrome and hemimegalencephaly
|
[NCBI]
|
8.44817e-05
|
|
|
trichodiscomas, familial multiple
|
[NCBI]
|
8.44817e-05
|
|
|
hypothalamic hamartomas
|
[NCBI]
|
8.44817e-05
|
|
|
NF2
|
[NCBI]
|
7.10824e-05
|
|
|
trichoepitheliomas, multiple desmoplastic
|
[NCBI]
|
7.05353e-05
|
|
|
NF1
|
[NCBI]
|
6.96508e-05
|
|
|
GNRH1
|
[NCBI]
|
6.84373e-05
|
|
|
MLRD
|
[NCBI]
|
6.64614e-05
|
|
|
KRT13
|
[NCBI]
|
6.53848e-05
|
|
|
FRAP1
|
[NCBI]
|
6.44202e-05
|
|
|
JPHT
|
[NCBI]
|
6.32194e-05
|
|
|
polydactyly, postaxial, type a1
|
[NCBI]
|
5.82253e-05
|
|
|
KRT6A
|
[NCBI]
|
5.68123e-05
|
|
|
SMOH
|
[NCBI]
|
5.68123e-05
|
|
|
GLI2
|
[NCBI]
|
5.68123e-05
|
|
|
schwannomatosis
|
[NCBI]
|
5.13775e-05
|
|
|
oculocerebrocutaneous syndrome
|
[NCBI]
|
5.13775e-05
|
|
|
GLI
|
[NCBI]
|
5.06447e-05
|
|
|
KRT16
|
[NCBI]
|
5.06447e-05
|
|
|
MUC1
|
[NCBI]
|
4.61984e-05
|
|
|
EPPK
|
[NCBI]
|
4.56329e-05
|
|
|
FLCN
|
[NCBI]
|
4.49835e-05
|
|
|
SYP
|
[NCBI]
|
4.49835e-05
|
|
|
HRPT2
|
[NCBI]
|
4.38219e-05
|
|
|
SMMCI
|
[NCBI]
|
4.38219e-05
|
|
|
CEACAM5
|
[NCBI]
|
4.24243e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
4.14514e-05
|
|
|
BCNS
|
[NCBI]
|
4.12413e-05
|
|
|
USH1C
|
[NCBI]
|
4.08287e-05
|
|
|
JBS
|
[NCBI]
|
4.00534e-05
|
|
|
HMGA2
|
[NCBI]
|
3.87956e-05
|
|
|
PTCH1
|
[NCBI]
|
3.87956e-05
|
|
|
OFD1
|
[NCBI]
|
3.75932e-05
|
|
|
CEACAM1
|
[NCBI]
|
3.44275e-05
|
|
|
STK11
|
[NCBI]
|
3.25651e-05
|
|
|
AFP
|
[NCBI]
|
3.24543e-05
|
|
|
sotos syndrome
|
[NCBI]
|
2.68273e-05
|
|
|
MKS1
|
[NCBI]
|
2.57874e-05
|
|
|
MEN1
|
[NCBI]
|
2.20002e-05
|
|
|
PTEN
|
[NCBI]
|
2.09556e-05
|
|
|
GFAP
|
[NCBI]
|
1.90989e-05
|
|
|
SHH
|
[NCBI]
|
1.27444e-05
|
|
|
AIS
|
[NCBI]
|
1.06751e-05
|
|
|
LAM
|
[NCBI]
|
1.00722e-05
|
|
|
VEGF
|
[NCBI]
|
7.29748e-06
|
|
|
PCNA
|
[NCBI]
|
4.74265e-06
|
|
|
polycystic kidneys
|
[NCBI]
|
2.74466e-06
|
|
|
CRH
|
[NCBI]
|
1.86516e-06
|
|
|
EGF
|
[NCBI]
|
9.69231e-07
|
|
|
APOE
|
[NCBI]
|
6.35292e-07
|
|
|
EGFR
|
[NCBI]
|
1.50614e-07
|
|