|
OMIM |
Link |
Information gain |
01 |
|
NPS
|
[NCBI]
|
0.0079001
|
|
|
PTLAH
|
[NCBI]
|
0.00098052
|
|
|
radial heads, posterior dislocation of
|
[NCBI]
|
0.00098052
|
|
|
LMX1B
|
[NCBI]
|
0.000971728
|
|
|
koilonychia, hereditary
|
[NCBI]
|
0.000844965
|
|
|
deafness, congenital, and onychodystrophy, recessive form
|
[NCBI]
|
0.000632907
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000450974
|
|
|
AK1
|
[NCBI]
|
0.000183798
|
|
|
ABO
|
[NCBI]
|
0.000124512
|
|
|
COL5A1
|
[NCBI]
|
0.000124512
|
|
|
nail-patella-like renal disease
|
[NCBI]
|
0.000116948
|
|
|
GLC1A
|
[NCBI]
|
0.000107551
|
|
|
POAG
|
[NCBI]
|
0.000107551
|
|
|
ASS
|
[NCBI]
|
8.97759e-05
|
|
|
TBX4
|
[NCBI]
|
7.59186e-05
|
|
|
SPS
|
[NCBI]
|
7.31844e-05
|
|
|
ehlers-danlos syndrome, type ii
|
[NCBI]
|
6.12812e-05
|
|
|
HHT
|
[NCBI]
|
2.86036e-05
|
|
|
BCNS
|
[NCBI]
|
1.94512e-05
|
|
|
FMF
|
[NCBI]
|
3.75183e-06
|
|