|
OMIM |
Link |
Information gain |
01 |
|
AKE
|
[NCBI]
|
0.00357597
|
|
|
PXE
|
[NCBI]
|
0.00276376
|
|
|
EPS
|
[NCBI]
|
0.00211333
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.00189459
|
|
|
focal facial dermal dysplasia
|
[NCBI]
|
0.00101143
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
0.000978677
|
|
|
collagenosis, familial reactive perforating
|
[NCBI]
|
0.00095499
|
|
|
aortic aneurysm, familial thoracic 1
|
[NCBI]
|
0.000910064
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
0.000840831
|
|
|
SVAS
|
[NCBI]
|
0.000571409
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
0.000549855
|
|
|
MFS
|
[NCBI]
|
0.000402108
|
|
|
RA
|
[NCBI]
|
0.000266888
|
|
|
WSS
|
[NCBI]
|
0.000243315
|
|
|
buschke-ollendorff syndrome
|
[NCBI]
|
0.000220333
|
|
|
ATS
|
[NCBI]
|
0.000214388
|
|
|
temporal arteritis
|
[NCBI]
|
0.000168828
|
|
|
tracheobronchomegaly
|
[NCBI]
|
0.000141472
|
|
|
takayasu arteritis
|
[NCBI]
|
0.000141472
|
|
|
AMVC
|
[NCBI]
|
0.000141472
|
|
|
epidermolysis bullosa pruriginosa
|
[NCBI]
|
0.000126695
|
|
|
acrogeria, gottron type
|
[NCBI]
|
0.000126695
|
|
|
ELN
|
[NCBI]
|
0.000111079
|
|
|
ehlers-danlos syndrome, type iii
|
[NCBI]
|
0.000110004
|
|
|
FBLN5
|
[NCBI]
|
9.98349e-05
|
|
|
sulfocysteinuria
|
[NCBI]
|
9.96511e-05
|
|
|
pseudoxanthoma elasticum, forme fruste
|
[NCBI]
|
9.96511e-05
|
|
|
LOXL1
|
[NCBI]
|
9.71799e-05
|
|
|
EMILIN1
|
[NCBI]
|
9.71799e-05
|
|
|
CF
|
[NCBI]
|
9.57805e-05
|
|
|
cutis laxa, autosomal recessive, type ii
|
[NCBI]
|
9.56376e-05
|
|
|
morquio syndrome b
|
[NCBI]
|
9.21347e-05
|
|
|
ABCC6
|
[NCBI]
|
7.77799e-05
|
|
|
GACI
|
[NCBI]
|
7.54371e-05
|
|
|
GLB1
|
[NCBI]
|
7.30302e-05
|
|
|
EFE
|
[NCBI]
|
6.91225e-05
|
|
|
LOX
|
[NCBI]
|
6.37655e-05
|
|
|
microfibril-associated glycoprotein 2
|
[NCBI]
|
6.35432e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
6.28937e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
6.28937e-05
|
|
|
costello syndrome
|
[NCBI]
|
5.78709e-05
|
|
|
SLE
|
[NCBI]
|
5.50939e-05
|
|
|
LSA
|
[NCBI]
|
5.44596e-05
|
|
|
MFAP4
|
[NCBI]
|
5.35606e-05
|
|
|
hurler syndrome
|
[NCBI]
|
5.07576e-05
|
|
|
EFEMP2
|
[NCBI]
|
4.97933e-05
|
|
|
LTBP4
|
[NCBI]
|
4.97933e-05
|
|
|
MFAP1
|
[NCBI]
|
4.73473e-05
|
|
|
TNXB
|
[NCBI]
|
3.66197e-05
|
|
|
homocystinuria
|
[NCBI]
|
2.80087e-05
|
|
|
SMS
|
[NCBI]
|
2.58558e-05
|
|
|
PI
|
[NCBI]
|
2.12875e-05
|
|
|
NF1
|
[NCBI]
|
1.91501e-05
|
|
|
WBS
|
[NCBI]
|
1.88196e-05
|
|
|
VEGF
|
[NCBI]
|
1.57519e-05
|
|
|
GJA1
|
[NCBI]
|
1.45485e-05
|
|
|
CEACAM5
|
[NCBI]
|
4.0235e-06
|
|
|
CRC
|
[NCBI]
|
9.99704e-07
|
|
|
EGF
|
[NCBI]
|
5.44209e-07
|
|
|
NGFB
|
[NCBI]
|
5.10727e-08
|
|