|
OMIM |
Link |
Information gain |
01 |
|
CHH
|
[NCBI]
|
0.00138289
|
|
|
SEMDIT
|
[NCBI]
|
0.000991404
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.000898321
|
|
|
ATD1
|
[NCBI]
|
0.000574326
|
|
|
keutel syndrome
|
[NCBI]
|
0.00041326
|
|
|
kniest dysplasia
|
[NCBI]
|
0.000149286
|
|
|
AGC1
|
[NCBI]
|
0.000139563
|
|
|
RMRP
|
[NCBI]
|
0.000131453
|
|
|
syndesmodysplasic dwarfism
|
[NCBI]
|
0.000122157
|
|
|
tracheopathia osteoplastica
|
[NCBI]
|
0.000122157
|
|
|
spondylometaphyseal dysplasia with dentinogenesis imperfecta
|
[NCBI]
|
9.12196e-05
|
|
|
COL2A1
|
[NCBI]
|
8.9064e-05
|
|
|
TLPD
|
[NCBI]
|
8.57198e-05
|
|
|
ACG1B
|
[NCBI]
|
8.57198e-05
|
|
|
winchester syndrome
|
[NCBI]
|
7.13328e-05
|
|
|
MGP
|
[NCBI]
|
6.79265e-05
|
|
|
EVC
|
[NCBI]
|
6.54159e-05
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
5.96965e-05
|
|
|
MCDS
|
[NCBI]
|
5.8804e-05
|
|
|
PPAC
|
[NCBI]
|
5.56645e-05
|
|
|
HSS
|
[NCBI]
|
5.4968e-05
|
|
|
pfeiffer syndrome
|
[NCBI]
|
4.97884e-05
|
|
|
HCH
|
[NCBI]
|
4.88374e-05
|
|
|
BMP2
|
[NCBI]
|
4.85725e-05
|
|
|
COL10A1
|
[NCBI]
|
4.74273e-05
|
|
|
SPARC
|
[NCBI]
|
4.74273e-05
|
|
|
EVC
|
[NCBI]
|
4.70932e-05
|
|
|
LNS
|
[NCBI]
|
3.8473e-05
|
|
|
IHH
|
[NCBI]
|
3.81156e-05
|
|
|
GUSB
|
[NCBI]
|
3.55467e-05
|
|
|
BGLAP
|
[NCBI]
|
3.26803e-05
|
|
|
SLE
|
[NCBI]
|
2.94501e-05
|
|
|
DBA
|
[NCBI]
|
2.91741e-05
|
|
|
COMP
|
[NCBI]
|
2.84684e-05
|
|
|
GAPDH
|
[NCBI]
|
2.31006e-05
|
|
|
RA
|
[NCBI]
|
1.35353e-05
|
|
|
MPO
|
[NCBI]
|
6.06349e-06
|
|
|
VEGF
|
[NCBI]
|
5.78117e-08
|
|