|
OMIM |
Link |
Information gain |
01 |
|
amelogenesis imperfecta, hypoplastic type
|
[NCBI]
|
0.003153
|
|
|
kohlschutter-tonz syndrome
|
[NCBI]
|
0.00232174
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.00165256
|
|
|
ameloonychohypohidrotic syndrome
|
[NCBI]
|
0.0010375
|
|
|
singleton-merten syndrome
|
[NCBI]
|
0.000819746
|
|
|
ODDD
|
[NCBI]
|
0.000667141
|
|
|
cenani syndactylism
|
[NCBI]
|
0.000644945
|
|
|
oculocerebral syndrome with hypopigmentation
|
[NCBI]
|
0.00056504
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
0.000440632
|
|
|
amelogenesis imperfecta, hypoplastic, and openbite malocclusion, autosomal recessive
|
[NCBI]
|
0.000211065
|
|
|
TS
|
[NCBI]
|
0.000201644
|
|
|
AIH2
|
[NCBI]
|
0.000164793
|
|
|
lenz-majewski hyperostotic dwarfism
|
[NCBI]
|
0.000160965
|
|
|
SRS
|
[NCBI]
|
0.000147464
|
|
|
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1
|
[NCBI]
|
0.000146647
|
|
|
enamel hypoplasia, cataracts, and aqueductal stenosis
|
[NCBI]
|
0.000120847
|
|
|
trichoodontoonychial dysplasia
|
[NCBI]
|
0.000120847
|
|
|
pfeiffer-palm-teller syndrome
|
[NCBI]
|
0.000120847
|
|
|
neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia
|
[NCBI]
|
0.000120847
|
|
|
AI1G
|
[NCBI]
|
8.99103e-05
|
|
|
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus
|
[NCBI]
|
8.99103e-05
|
|
|
GJA1
|
[NCBI]
|
8.98935e-05
|
|
|
hearing loss, sensorineural, with enamel hypoplasia and nail defects
|
[NCBI]
|
8.44113e-05
|
|
|
AIHHT
|
[NCBI]
|
7.70698e-05
|
|
|
syndactyly, type iii
|
[NCBI]
|
7.70698e-05
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
6.82323e-05
|
|
|
ENAM
|
[NCBI]
|
6.48204e-05
|
|
|
LADD
|
[NCBI]
|
6.38082e-05
|
|
|
AMELX
|
[NCBI]
|
6.23221e-05
|
|
|
seckel syndrome 1
|
[NCBI]
|
5.83982e-05
|
|
|
CIPA
|
[NCBI]
|
5.66621e-05
|
|
|
PITX2
|
[NCBI]
|
5.60041e-05
|
|
|
HSS
|
[NCBI]
|
5.36741e-05
|
|
|
RIEG1
|
[NCBI]
|
5.11628e-05
|
|
|
epidermolysis bullosa letalis
|
[NCBI]
|
5.05931e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
4.8838e-05
|
|
|
FGFR1
|
[NCBI]
|
4.40056e-05
|
|
|
costello syndrome
|
[NCBI]
|
4.06158e-05
|
|
|
RTS
|
[NCBI]
|
4.00394e-05
|
|
|
SLS
|
[NCBI]
|
3.42435e-05
|
|
|
SVAS
|
[NCBI]
|
3.38643e-05
|
|
|
APS1
|
[NCBI]
|
3.03834e-05
|
|
|
CD
|
[NCBI]
|
2.71671e-05
|
|
|
CFTR
|
[NCBI]
|
1.90616e-05
|
|
|
CF
|
[NCBI]
|
8.22569e-06
|
|
|
PWS
|
[NCBI]
|
5.2256e-06
|
|