|
OMIM |
Link |
Information
gain |
01 |
|
|
acrodysostosis
|
[NCBI]
|
0.00161608
|
|
|
|
osteodysplasia, familial, anderson type
|
[NCBI]
|
0.000948879
|
|
|
|
brachydactyly-mental retardation syndrome
|
[NCBI]
|
0.000813359
|
|
|
|
ADFN
|
[NCBI]
|
0.000640751
|
|
|
|
mohr syndrome
|
[NCBI]
|
0.000601472
|
|
|
|
TRPS1
|
[NCBI]
|
0.000353134
|
|
|
|
blepharonasofacial malformation syndrome
|
[NCBI]
|
0.000261456
|
|
|
|
WS1
|
[NCBI]
|
0.000199441
|
|
|
|
JBS
|
[NCBI]
|
0.00014997
|
|
|
|
TRPS2
|
[NCBI]
|
0.000130533
|
|
|
|
frontonasal dysplasia with alar clefts
|
[NCBI]
|
0.000130439
|
|
|
|
bifid nose
|
[NCBI]
|
0.000130439
|
|
|
|
bird-headed dwarfism, montreal type
|
[NCBI]
|
0.000130439
|
|
|
|
mental retardation syndrome, mietens-weber type
|
[NCBI]
|
0.000107971
|
|
|
|
aniridia, partial, with unilateral renal agenesis and psychomotor retardation
|
[NCBI]
|
0.000107971
|
|
|
|
arhinia, choanal atresia, and microphthalmia
|
[NCBI]
|
9.9494e-05
|
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
9.9494e-05
|
|
|
|
tietz syndrome
|
[NCBI]
|
8.98999e-05
|
|
|
|
BDE
|
[NCBI]
|
8.16129e-05
|
|
|
|
PBT
|
[NCBI]
|
7.335e-05
|
|
|
|
marshall syndrome
|
[NCBI]
|
6.98767e-05
|
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
6.98767e-05
|
|
|
|
CDPX1
|
[NCBI]
|
6.7023e-05
|
|
|
|
OFD1
|
[NCBI]
|
6.06417e-05
|
|
|
|
fraser syndrome
|
[NCBI]
|
5.84605e-05
|
|
|
|
RCDP1
|
[NCBI]
|
5.60976e-05
|
|
|
|
GCPS
|
[NCBI]
|
5.29257e-05
|
|
|
|
ED1
|
[NCBI]
|
4.99856e-05
|
|
|
|
WBS
|
[NCBI]
|
2.94723e-05
|
|
