|
OMIM |
Link |
Information
gain |
01 |
|
|
ameloonychohypohidrotic syndrome
|
[NCBI]
|
0.00129156
|
|
|
|
amelogenesis imperfecta, hypoplastic type
|
[NCBI]
|
0.000991404
|
|
|
|
cholestasis-lymphedema syndrome
|
[NCBI]
|
0.000866698
|
|
|
|
erythema of acral regions
|
[NCBI]
|
0.000154415
|
|
|
|
sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth
|
[NCBI]
|
0.000154415
|
|
|
|
dentin dysplasia, type ii
|
[NCBI]
|
0.000105561
|
|
|
|
AIH2
|
[NCBI]
|
0.00010353
|
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
0.000101727
|
|
|
|
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus
|
[NCBI]
|
0.000100104
|
|
|
|
DGI1
|
[NCBI]
|
9.37927e-05
|
|
|
|
periodontitis, aggressive, 1
|
[NCBI]
|
8.84935e-05
|
|
|
|
NFE2L2
|
[NCBI]
|
8.57716e-05
|
|
|
|
ODDD
|
[NCBI]
|
8.03786e-05
|
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
6.49988e-05
|
|
|
|
CF
|
[NCBI]
|
3.44722e-06
|
|
