|
OMIM |
Link |
Information gain |
01 |
|
AOS
|
[NCBI]
|
0.0331811
|
|
|
ACC
|
[NCBI]
|
0.0110131
|
|
|
alopecia, androgenetic
|
[NCBI]
|
0.00170865
|
|
|
schimmelpenning-feuerstein-mims syndrome
|
[NCBI]
|
0.00127919
|
|
|
spiegler-brooke syndrome
|
[NCBI]
|
0.00119838
|
|
|
hypotrichosis simplex of scalp
|
[NCBI]
|
0.00108721
|
|
|
acromegaloid changes, cutis verticis gyrata, and corneal leukoma
|
[NCBI]
|
0.00106213
|
|
|
knobloch syndrome, type ii
|
[NCBI]
|
0.000753098
|
|
|
MHAC
|
[NCBI]
|
0.000753098
|
|
|
TRICY1
|
[NCBI]
|
0.000753098
|
|
|
CVG/MR
|
[NCBI]
|
0.000723468
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
0.000652627
|
|
|
trichohepatoenteric syndrome
|
[NCBI]
|
0.000563413
|
|
|
scalp defects and postaxial polydactyly
|
[NCBI]
|
0.000542106
|
|
|
hypotrichosis, marie unna type
|
[NCBI]
|
0.000429886
|
|
|
KNO
|
[NCBI]
|
0.000380083
|
|
|
DFSP
|
[NCBI]
|
0.000337618
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.000330024
|
|
|
KFSD
|
[NCBI]
|
0.000318318
|
|
|
JBS
|
[NCBI]
|
0.000303382
|
|
|
fibromatosis, juvenile hyaline
|
[NCBI]
|
0.000233905
|
|
|
EV
|
[NCBI]
|
0.000205945
|
|
|
ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features
|
[NCBI]
|
0.000180376
|
|
|
alopecia, familial focal
|
[NCBI]
|
0.000180376
|
|
|
ACCCA
|
[NCBI]
|
0.000180376
|
|
|
cutis verticis gyrata, thyroid aplasia, and mental retardation
|
[NCBI]
|
0.000180376
|
|
|
cardiomyopathy, congestive, with hypergonadotropic hypogonadism
|
[NCBI]
|
0.000180376
|
|
|
AIC
|
[NCBI]
|
0.000167422
|
|
|
CMTC
|
[NCBI]
|
0.000158188
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000147416
|
|
|
pilomatrixoma
|
[NCBI]
|
0.000141147
|
|
|
S PEAK SYNDROME
|
[NCBI]
|
0.000141147
|
|
|
cardiomyopathy-hypogonadism-collagenoma syndrome
|
[NCBI]
|
0.000141147
|
|
|
SLE
|
[NCBI]
|
0.000139509
|
|
|
poland syndrome
|
[NCBI]
|
0.000130099
|
|
|
aplasia cutis congenita with epibulbar dermoids
|
[NCBI]
|
0.00012637
|
|
|
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
|
[NCBI]
|
0.00012637
|
|
|
CDSN
|
[NCBI]
|
0.000125941
|
|
|
KRTAP1-4
|
[NCBI]
|
0.000122702
|
|
|
KRTAP1-3
|
[NCBI]
|
0.000122702
|
|
|
KRTAP1-5
|
[NCBI]
|
0.000122702
|
|
|
KRTAP1-1
|
[NCBI]
|
0.000122702
|
|
|
hair whorl
|
[NCBI]
|
0.000116791
|
|
|
temporal arteritis
|
[NCBI]
|
0.00010326
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000101644
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
9.93288e-05
|
|
|
ALUNC
|
[NCBI]
|
9.93288e-05
|
|
|
APL
|
[NCBI]
|
9.53158e-05
|
|
|
phace association
|
[NCBI]
|
9.53158e-05
|
|
|
osseous heteroplasia, progressive
|
[NCBI]
|
9.53158e-05
|
|
|
SRD5A1
|
[NCBI]
|
9.52032e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
9.18134e-05
|
|
|
RHS
|
[NCBI]
|
9.18134e-05
|
|
|
hemangioma-thrombocytopenia syndrome
|
[NCBI]
|
9.18134e-05
|
|
|
PPSH
|
[NCBI]
|
7.69615e-05
|
|
|
GABEB
|
[NCBI]
|
7.33963e-05
|
|
|
MTS
|
[NCBI]
|
6.88074e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
6.37138e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
5.84901e-05
|
|
|
AR
|
[NCBI]
|
5.74747e-05
|
|
|
HGPS
|
[NCBI]
|
4.60592e-05
|
|
|
APS1
|
[NCBI]
|
4.60592e-05
|
|
|
LNS
|
[NCBI]
|
4.33476e-05
|
|
|
SRD5A2
|
[NCBI]
|
4.17991e-05
|
|
|
DSG4
|
[NCBI]
|
3.86626e-05
|
|
|
KRTHA1
|
[NCBI]
|
3.86626e-05
|
|
|
HSR
|
[NCBI]
|
3.71422e-05
|
|
|
CLDN1
|
[NCBI]
|
3.48222e-05
|
|
|
SFRP1
|
[NCBI]
|
3.19947e-05
|
|
|
fabry disease
|
[NCBI]
|
3.18973e-05
|
|
|
COL17A1
|
[NCBI]
|
3.13569e-05
|
|
|
MUC1
|
[NCBI]
|
3.11653e-05
|
|
|
BCNS
|
[NCBI]
|
3.04118e-05
|
|
|
KRT20
|
[NCBI]
|
2.42552e-05
|
|
|
AIS
|
[NCBI]
|
2.34599e-05
|
|
|
HPRT1
|
[NCBI]
|
2.12887e-05
|
|
|
CALCRL
|
[NCBI]
|
2.02697e-05
|
|
|
CDK2
|
[NCBI]
|
1.5211e-05
|
|
|
TLR2
|
[NCBI]
|
1.5211e-05
|
|
|
SHBG
|
[NCBI]
|
1.06441e-05
|
|
|
CYP1A1
|
[NCBI]
|
9.71336e-06
|
|
|
SLC6A3
|
[NCBI]
|
7.90115e-06
|
|
|
TG
|
[NCBI]
|
7.65004e-06
|
|
|
POMC
|
[NCBI]
|
7.3782e-06
|
|
|
G6PD
|
[NCBI]
|
6.34386e-06
|
|
|
GDNF
|
[NCBI]
|
5.94345e-06
|
|
|
TNFSF6
|
[NCBI]
|
4.23805e-06
|
|
|
AFP
|
[NCBI]
|
4.05694e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
3.24498e-06
|
|
|
CEACAM5
|
[NCBI]
|
2.48692e-06
|
|
|
NGFB
|
[NCBI]
|
1.59323e-06
|
|
|
PCNA
|
[NCBI]
|
1.15736e-06
|
|
|
VEGF
|
[NCBI]
|
1.03512e-06
|
|
|
PD
|
[NCBI]
|
6.87331e-07
|
|
|
APC
|
[NCBI]
|
5.02038e-07
|
|
|
GFAP
|
[NCBI]
|
4.36686e-07
|
|
|
PRL
|
[NCBI]
|
7.20835e-08
|
|
|
EGF
|
[NCBI]
|
8.25172e-09
|
|