|
OMIM |
Link |
Information gain |
01 |
|
hypobetalipoproteinemia, familial, 2
|
[NCBI]
|
0.00390348
|
|
|
APOB
|
[NCBI]
|
0.00266592
|
|
|
ABL
|
[NCBI]
|
0.000461875
|
|
|
hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration
|
[NCBI]
|
0.000108698
|
|
|
SLOS
|
[NCBI]
|
0.000107369
|
|
|
anderson disease
|
[NCBI]
|
0.000101342
|
|
|
CMRD
|
[NCBI]
|
9.63076e-05
|
|
|
legg-calve-perthes disease
|
[NCBI]
|
9.24751e-05
|
|
|
PCSK9
|
[NCBI]
|
4.8838e-05
|
|
|
SMAX1
|
[NCBI]
|
4.85035e-05
|
|
|
PANK2
|
[NCBI]
|
3.79639e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
2.76438e-05
|
|
|
RP
|
[NCBI]
|
2.45732e-05
|
|
|
LPL
|
[NCBI]
|
2.66222e-06
|
|
|
APOE
|
[NCBI]
|
5.18362e-07
|
|