|
OMIM |
Link |
Information
gain |
01 |
|
|
poland syndrome
|
[NCBI]
|
0.00158883
|
|
|
|
ear malformation
|
[NCBI]
|
0.00103373
|
|
|
|
aural atresia, congenital
|
[NCBI]
|
0.00103373
|
|
|
|
prognathism, mandibular
|
[NCBI]
|
0.000869022
|
|
|
|
ACC
|
[NCBI]
|
0.000782567
|
|
|
|
maxillonasal dysplasia, binder type
|
[NCBI]
|
0.000750736
|
|
|
|
mohr syndrome
|
[NCBI]
|
0.000699741
|
|
|
|
HFM
|
[NCBI]
|
0.000347042
|
|
|
|
curved nail of fourth toe
|
[NCBI]
|
0.000165625
|
|
|
|
frontonasal dysplasia with alar clefts
|
[NCBI]
|
0.000165625
|
|
|
|
ear folding
|
[NCBI]
|
0.000137856
|
|
|
|
arhinia, choanal atresia, and microphthalmia
|
[NCBI]
|
0.000137856
|
|
|
|
torticollis
|
[NCBI]
|
0.000137856
|
|
|
|
breasts and nipples, absence of
|
[NCBI]
|
0.000127378
|
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
0.000115518
|
|
|
|
whistling face syndrome, recessive form
|
[NCBI]
|
0.000111489
|
|
|
|
SYM1
|
[NCBI]
|
0.000102766
|
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
9.50532e-05
|
|
|
|
CFEOM1
|
[NCBI]
|
9.35156e-05
|
|
|
|
DA2A
|
[NCBI]
|
8.6176e-05
|
|
|
|
HHT
|
[NCBI]
|
6.8065e-05
|
|
|
|
TCOF
|
[NCBI]
|
6.43592e-05
|
|
|
|
alopecia, androgenetic
|
[NCBI]
|
6.06811e-05
|
|
|
|
PXE
|
[NCBI]
|
4.72163e-05
|
|
|
|
DFSP
|
[NCBI]
|
4.44123e-05
|
|
|
|
CPI
|
[NCBI]
|
4.1268e-05
|
|
|
|
GJA1
|
[NCBI]
|
2.55658e-05
|
|
|
|
FGF7
|
[NCBI]
|
2.36448e-05
|
|
|
|
RA
|
[NCBI]
|
1.718e-05
|
|
|
|
CJD
|
[NCBI]
|
1.54848e-05
|
|
|
|
BDNF
|
[NCBI]
|
1.32729e-05
|
|
|
|
VEGF
|
[NCBI]
|
6.76489e-06
|
|
|
|
EGF
|
[NCBI]
|
6.24988e-06
|
|
