|
OMIM |
Link |
Information gain |
01 |
|
CMT2G
|
[NCBI]
|
0.00102023
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.000844965
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.000711792
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000672411
|
|
|
RA
|
[NCBI]
|
0.000381391
|
|
|
pseudodiastrophic dysplasia
|
[NCBI]
|
8.84935e-05
|
|
|
CMT2A2
|
[NCBI]
|
8.07248e-05
|
|
|
CMT2A1
|
[NCBI]
|
7.79043e-05
|
|
|
SLE
|
[NCBI]
|
1.56838e-06
|
|