|
OMIM |
Link |
Information
gain |
01 |
|
|
chiari malformation type i
|
[NCBI]
|
0.000925375
|
|
|
|
megarbane syndrome
|
[NCBI]
|
0.000154415
|
|
|
|
plantar lipomatosis, unusual facies, and developmental delay
|
[NCBI]
|
0.000131943
|
|
|
|
carpenter syndrome
|
[NCBI]
|
0.000107884
|
|
|
|
young syndrome
|
[NCBI]
|
0.000107884
|
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
8.84935e-05
|
|
|
|
INSL3
|
[NCBI]
|
8.55726e-05
|
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
7.94923e-05
|
|
|
|
CF
|
[NCBI]
|
3.44722e-06
|
|
