|
OMIM |
Link |
Information gain |
01 |
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.00621054
|
|
|
hydrocephalus, autosomal dominant
|
[NCBI]
|
0.00148718
|
|
|
mesomelic dysplasia, kantaputra type
|
[NCBI]
|
0.00105937
|
|
|
spondylometaphyseal dysplasia, kozlowski type
|
[NCBI]
|
0.00105937
|
|
|
DURS1
|
[NCBI]
|
0.000738236
|
|
|
spondylocarpotarsal synostosis syndrome
|
[NCBI]
|
0.00067775
|
|
|
ATD1
|
[NCBI]
|
0.000504545
|
|
|
patent ductus arteriosus and bicuspid aortic valve with hand anomalies
|
[NCBI]
|
0.000202202
|
|
|
BDA6
|
[NCBI]
|
0.000202202
|
|
|
symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch
|
[NCBI]
|
0.000202202
|
|
|
bor-duane hydrocephalus contiguous gene syndrome
|
[NCBI]
|
0.000202202
|
|
|
megaepiphyseal dwarfism
|
[NCBI]
|
0.000202202
|
|
|
osteoid osteoma
|
[NCBI]
|
0.000202202
|
|
|
LWD
|
[NCBI]
|
0.000195634
|
|
|
devriendt syndrome
|
[NCBI]
|
0.000162947
|
|
|
second metatarsal-metacarpal syndrome
|
[NCBI]
|
0.000162947
|
|
|
humeroradial synostosis
|
[NCBI]
|
0.000162947
|
|
|
TCC
|
[NCBI]
|
0.000148144
|
|
|
MADB
|
[NCBI]
|
0.000138539
|
|
|
winchester syndrome
|
[NCBI]
|
0.000131402
|
|
|
RA
|
[NCBI]
|
0.00011957
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
0.000110298
|
|
|
weaver syndrome
|
[NCBI]
|
0.000100424
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
9.84211e-05
|
|
|
BGS
|
[NCBI]
|
8.37791e-05
|
|
|
EVC
|
[NCBI]
|
8.26677e-05
|
|
|
DA2A
|
[NCBI]
|
8.16e-05
|
|
|
BOR1
|
[NCBI]
|
8.05727e-05
|
|
|
CRMO
|
[NCBI]
|
7.05796e-05
|
|
|
HOS
|
[NCBI]
|
6.49643e-05
|
|
|
HHT
|
[NCBI]
|
6.38639e-05
|
|
|
HOXA11
|
[NCBI]
|
5.96594e-05
|
|
|
HOXD13
|
[NCBI]
|
4.64755e-05
|
|
|
NOG
|
[NCBI]
|
4.28919e-05
|
|
|
GJA5
|
[NCBI]
|
4.16036e-05
|
|
|
SLE
|
[NCBI]
|
3.94837e-05
|
|
|
FGFR3
|
[NCBI]
|
2.99965e-05
|
|
|
COMP
|
[NCBI]
|
2.79085e-05
|
|
|
TTR
|
[NCBI]
|
2.3648e-05
|
|
|
TNF
|
[NCBI]
|
3.1454e-06
|
|