|
OMIM |
Link |
Information gain |
01 |
|
flynn-aird syndrome
|
[NCBI]
|
0.00129156
|
|
|
curly hair-acral keratoderma-caries syndrome
|
[NCBI]
|
0.00129156
|
|
|
johnson neuroectodermal syndrome
|
[NCBI]
|
0.000938013
|
|
|
ALSG
|
[NCBI]
|
0.000183236
|
|
|
erythema of acral regions
|
[NCBI]
|
0.000127818
|
|
|
DSPP
|
[NCBI]
|
0.000116063
|
|
|
FOP
|
[NCBI]
|
0.000105792
|
|
|
acrofacial dysostosis, catania type
|
[NCBI]
|
0.000105351
|
|
|
dyskeratosis congenita, autosomal recessive
|
[NCBI]
|
9.13729e-05
|
|
|
GDF11
|
[NCBI]
|
7.8499e-05
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
7.51743e-05
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
7.51743e-05
|
|
|
PC1
|
[NCBI]
|
6.94982e-05
|
|
|
ED2
|
[NCBI]
|
6.53139e-05
|
|
|
immunoosseous dysplasia, schimke type
|
[NCBI]
|
6.44189e-05
|
|
|
SMMCI
|
[NCBI]
|
6.44189e-05
|
|
|
hypophosphatasia, adult type
|
[NCBI]
|
6.44189e-05
|
|
|
SOST
|
[NCBI]
|
6.35713e-05
|
|
|
DKC
|
[NCBI]
|
5.22474e-05
|
|
|
SCS
|
[NCBI]
|
5.03452e-05
|
|
|
FDH
|
[NCBI]
|
5.03452e-05
|
|
|
ALPL
|
[NCBI]
|
5.01662e-05
|
|
|
CSA
|
[NCBI]
|
4.77133e-05
|
|
|
fructose intolerance, hereditary
|
[NCBI]
|
4.63428e-05
|
|
|
SLS
|
[NCBI]
|
4.09525e-05
|
|
|
NGFR
|
[NCBI]
|
3.92901e-05
|
|
|
SDS
|
[NCBI]
|
3.91145e-05
|
|
|
GAL
|
[NCBI]
|
3.54884e-05
|
|
|
GHR
|
[NCBI]
|
3.47314e-05
|
|
|
NPY
|
[NCBI]
|
3.43457e-05
|
|
|
TLR2
|
[NCBI]
|
3.4029e-05
|
|
|
CF
|
[NCBI]
|
3.34686e-05
|
|
|
ADM
|
[NCBI]
|
3.21217e-05
|
|
|
GJA1
|
[NCBI]
|
3.15807e-05
|
|
|
SLE
|
[NCBI]
|
2.9748e-05
|
|
|
MBL2
|
[NCBI]
|
2.80904e-05
|
|
|
WBS
|
[NCBI]
|
2.70323e-05
|
|
|
RA
|
[NCBI]
|
2.55535e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.45475e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
1.90281e-05
|
|
|
FA
|
[NCBI]
|
1.20313e-05
|
|
|
PWS
|
[NCBI]
|
9.95466e-06
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
8.22473e-06
|
|
|
PCNA
|
[NCBI]
|
6.40197e-06
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
3.82723e-06
|
|
|
VEGF
|
[NCBI]
|
4.33511e-07
|
|