|
OMIM |
Link |
Information gain |
01 |
|
SPG23
|
[NCBI]
|
0.00197819
|
|
|
SHEP2
|
[NCBI]
|
0.00151005
|
|
|
MC1R
|
[NCBI]
|
0.00135588
|
|
|
SHEP8
|
[NCBI]
|
0.00129874
|
|
|
frontofacionasal dysostosis
|
[NCBI]
|
0.000933827
|
|
|
OB10P
|
[NCBI]
|
0.000869022
|
|
|
oculocerebral syndrome with hypopigmentation
|
[NCBI]
|
0.000869022
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.000820886
|
|
|
acromegaloid facial appearance syndrome
|
[NCBI]
|
0.000820886
|
|
|
OSCS
|
[NCBI]
|
0.000782567
|
|
|
alopecia areata 1
|
[NCBI]
|
0.000598712
|
|
|
SHEP1
|
[NCBI]
|
0.000544675
|
|
|
proopiomelanocortin deficiency
|
[NCBI]
|
0.000429768
|
|
|
HPS
|
[NCBI]
|
0.00029534
|
|
|
SHEP9
|
[NCBI]
|
0.000286157
|
|
|
ASIP
|
[NCBI]
|
0.00027804
|
|
|
elejalde disease
|
[NCBI]
|
0.000209705
|
|
|
SHEP3
|
[NCBI]
|
0.000202332
|
|
|
WS2A
|
[NCBI]
|
0.000174511
|
|
|
HSCR2
|
[NCBI]
|
0.000171312
|
|
|
waardenburg-shah syndrome
|
[NCBI]
|
0.000168353
|
|
|
white forelock with malformations
|
[NCBI]
|
0.000142903
|
|
|
SHEP6
|
[NCBI]
|
0.000142903
|
|
|
osteopathia striata with pigmentary dermopathy including white forelock
|
[NCBI]
|
0.000142903
|
|
|
SHEP7
|
[NCBI]
|
0.000142903
|
|
|
TYR
|
[NCBI]
|
0.000137917
|
|
|
CHS
|
[NCBI]
|
0.000137394
|
|
|
OCA1A
|
[NCBI]
|
0.000130823
|
|
|
MITF
|
[NCBI]
|
0.000130156
|
|
|
LYST
|
[NCBI]
|
0.000127626
|
|
|
abcd syndrome
|
[NCBI]
|
0.000115145
|
|
|
ataxia-deafness-retardation syndrome
|
[NCBI]
|
0.000115145
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
0.000115145
|
|
|
oca2 gene
|
[NCBI]
|
0.000109585
|
|
|
TYRP1
|
[NCBI]
|
0.000107458
|
|
|
SHEP5
|
[NCBI]
|
0.000104677
|
|
|
POMC
|
[NCBI]
|
0.000103802
|
|
|
acth deficiency
|
[NCBI]
|
9.78856e-05
|
|
|
twinning, monozygotic
|
[NCBI]
|
8.54822e-05
|
|
|
GS1
|
[NCBI]
|
8.26262e-05
|
|
|
GS2
|
[NCBI]
|
8.01311e-05
|
|
|
WS3
|
[NCBI]
|
7.59254e-05
|
|
|
EDNRB
|
[NCBI]
|
7.32518e-05
|
|
|
KIT
|
[NCBI]
|
6.72234e-05
|
|
|
SLE
|
[NCBI]
|
6.58701e-05
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
6.57974e-05
|
|
|
MLPH
|
[NCBI]
|
6.1531e-05
|
|
|
CPX
|
[NCBI]
|
5.9166e-05
|
|
|
FDH
|
[NCBI]
|
5.9166e-05
|
|
|
SILV
|
[NCBI]
|
5.81054e-05
|
|
|
PWS
|
[NCBI]
|
5.70362e-05
|
|
|
ATRN
|
[NCBI]
|
5.54535e-05
|
|
|
OPA1
|
[NCBI]
|
5.19099e-05
|
|
|
AT
|
[NCBI]
|
5.01032e-05
|
|
|
MYO5A
|
[NCBI]
|
4.93971e-05
|
|
|
KITLG
|
[NCBI]
|
4.73002e-05
|
|
|
TERC
|
[NCBI]
|
4.61143e-05
|
|
|
TRAPPC6A
|
[NCBI]
|
4.56137e-05
|
|
|
ATP7A
|
[NCBI]
|
4.44489e-05
|
|
|
CHM
|
[NCBI]
|
4.3978e-05
|
|
|
alopecia, androgenetic
|
[NCBI]
|
3.87197e-05
|
|
|
BCL2
|
[NCBI]
|
3.7956e-05
|
|
|
TRAPPC6B
|
[NCBI]
|
3.73688e-05
|
|
|
MREG
|
[NCBI]
|
3.73688e-05
|
|
|
SLC24A4
|
[NCBI]
|
3.42586e-05
|
|
|
CNO
|
[NCBI]
|
3.42586e-05
|
|
|
HERC2
|
[NCBI]
|
3.42586e-05
|
|
|
HPS4
|
[NCBI]
|
3.22398e-05
|
|
|
HPS3
|
[NCBI]
|
3.22398e-05
|
|
|
ATM
|
[NCBI]
|
3.07994e-05
|
|
|
DEFB103A
|
[NCBI]
|
2.95441e-05
|
|
|
RABGGTA
|
[NCBI]
|
2.85507e-05
|
|
|
ALB
|
[NCBI]
|
2.78289e-05
|
|
|
HSCR1
|
[NCBI]
|
2.76139e-05
|
|
|
FOXN1
|
[NCBI]
|
2.62981e-05
|
|
|
NID
|
[NCBI]
|
2.5705e-05
|
|
|
RAB27A
|
[NCBI]
|
2.34005e-05
|
|
|
SLC45A2
|
[NCBI]
|
2.26838e-05
|
|
|
EDN3
|
[NCBI]
|
1.92251e-05
|
|
|
SOX10
|
[NCBI]
|
1.86922e-05
|
|
|
SNRPN
|
[NCBI]
|
1.76125e-05
|
|
|
DCT
|
[NCBI]
|
1.67045e-05
|
|
|
homocystinuria
|
[NCBI]
|
1.27445e-05
|
|
|
AS
|
[NCBI]
|
1.23122e-05
|
|
|
GC
|
[NCBI]
|
1.02503e-05
|
|
|
PRL
|
[NCBI]
|
2.85644e-06
|
|
|
CJD
|
[NCBI]
|
1.60657e-06
|
|
|
HGF
|
[NCBI]
|
2.12276e-08
|
|