|
OMIM |
Link |
Information gain |
01 |
|
MVP
|
[NCBI]
|
0.0101092
|
|
|
CVD1
|
[NCBI]
|
0.00162737
|
|
|
AVSD
|
[NCBI]
|
0.000456921
|
|
|
SLE
|
[NCBI]
|
0.000204826
|
|
|
CMH
|
[NCBI]
|
0.000184272
|
|
|
endocardial fibroelastosis and coarctation of abdominal aorta
|
[NCBI]
|
0.000120229
|
|
|
mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones
|
[NCBI]
|
0.000120229
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
0.000108008
|
|
|
RA
|
[NCBI]
|
9.65736e-05
|
|
|
orthostatic intolerance
|
[NCBI]
|
7.6454e-05
|
|
|
LAMB1
|
[NCBI]
|
6.37462e-05
|
|
|
CMD3B
|
[NCBI]
|
6.3195e-05
|
|
|
PF4
|
[NCBI]
|
6.29896e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
5.8494e-05
|
|
|
heart block, congenital
|
[NCBI]
|
5.68953e-05
|
|
|
PFHB1A
|
[NCBI]
|
5.23988e-05
|
|
|
gm1-gangliosidosis, type i
|
[NCBI]
|
4.7895e-05
|
|
|
neuraminidase deficiency with beta-galactosidase deficiency
|
[NCBI]
|
4.5103e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
4.44048e-05
|
|
|
aortic valve disease
|
[NCBI]
|
3.86174e-05
|
|
|
RSTS
|
[NCBI]
|
3.78357e-05
|
|
|
CLS
|
[NCBI]
|
3.70926e-05
|
|
|
hurler syndrome
|
[NCBI]
|
3.68529e-05
|
|
|
fabry disease
|
[NCBI]
|
2.77544e-05
|
|
|
EPO
|
[NCBI]
|
2.75552e-05
|
|
|
NF1
|
[NCBI]
|
2.51172e-05
|
|
|
WBS
|
[NCBI]
|
2.01657e-05
|
|
|
PPARA
|
[NCBI]
|
1.99584e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
1.78124e-05
|
|
|
MFS
|
[NCBI]
|
1.68424e-05
|
|
|
NPPA
|
[NCBI]
|
1.57943e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
1.12825e-05
|
|
|
TNF
|
[NCBI]
|
9.42308e-06
|
|
|
PCNA
|
[NCBI]
|
6.40197e-06
|
|