|
OMIM |
Link |
Information
gain |
01 |
|
|
distichiasis
|
[NCBI]
|
0.00782823
|
|
|
|
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina
|
[NCBI]
|
0.00557031
|
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.00395549
|
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
0.00282923
|
|
|
|
blepharocheilodontic syndrome
|
[NCBI]
|
0.00189564
|
|
|
|
trichomegaly
|
[NCBI]
|
0.000416015
|
|
|
|
OCP
|
[NCBI]
|
0.000313784
|
|
|
|
STALE
|
[NCBI]
|
0.000207578
|
|
|
|
hair defect with photosensitivity and mental retardation
|
[NCBI]
|
0.000207578
|
|
|
|
ectodermal dysplasia, hidrotic, christianson-fourie type
|
[NCBI]
|
0.000207578
|
|
|
|
woolly hair, hypotrichosis, everted lower lip, and outstanding ears
|
[NCBI]
|
0.000207578
|
|
|
|
distichiasis with congenital anomalies of the heart and peripheral vasculature
|
[NCBI]
|
0.000207578
|
|
|
|
FOXC2
|
[NCBI]
|
0.000180333
|
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
0.00016832
|
|
|
|
lymphedema and ptosis
|
[NCBI]
|
0.00016832
|
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
0.000122308
|
|
|
|
lymphedema, hereditary, i
|
[NCBI]
|
0.000118776
|
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
0.000118776
|
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
0.000103743
|
|
|
|
fraser syndrome
|
[NCBI]
|
9.02246e-05
|
|
|
|
WS1
|
[NCBI]
|
7.72396e-05
|
|
|
|
RSTS
|
[NCBI]
|
7.58042e-05
|
|
|
|
ED1
|
[NCBI]
|
7.13101e-05
|
|
|
|
IP
|
[NCBI]
|
4.99454e-05
|
|
|
|
BCHE
|
[NCBI]
|
3.21562e-05
|
|
|
|
RP
|
[NCBI]
|
1.5061e-05
|
|
|
|
EGFR
|
[NCBI]
|
1.30047e-05
|
|
