|
OMIM |
Link |
Information gain |
01 |
|
keratitis fugax hereditaria
|
[NCBI]
|
0.00252968
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
0.00126108
|
|
|
corneal hypesthesia, familial
|
[NCBI]
|
0.00102023
|
|
|
epidermolysis bullosa inversa dystrophica
|
[NCBI]
|
0.000844965
|
|
|
keratitis, hereditary
|
[NCBI]
|
0.00048012
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
0.000443196
|
|
|
MPO
|
[NCBI]
|
0.000189744
|
|
|
OCP
|
[NCBI]
|
0.000185838
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
0.000168802
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
0.000163493
|
|
|
dermatoosteolysis, kirghizian type
|
[NCBI]
|
0.000129339
|
|
|
TLR4
|
[NCBI]
|
0.00010883
|
|
|
ichthyosis, hystrix-like, with deafness
|
[NCBI]
|
0.000106872
|
|
|
APS1
|
[NCBI]
|
9.95461e-05
|
|
|
GJB2
|
[NCBI]
|
9.61778e-05
|
|
|
HSAN5
|
[NCBI]
|
8.55432e-05
|
|
|
keratoderma, palmoplantar, with deafness
|
[NCBI]
|
8.05159e-05
|
|
|
HRD
|
[NCBI]
|
7.5072e-05
|
|
|
KCS
|
[NCBI]
|
7.5072e-05
|
|
|
WZS
|
[NCBI]
|
7.22548e-05
|
|
|
MCDC1
|
[NCBI]
|
6.77742e-05
|
|
|
ED2
|
[NCBI]
|
6.68256e-05
|
|
|
EKV
|
[NCBI]
|
5.73722e-05
|
|
|
STL1
|
[NCBI]
|
5.41573e-05
|
|
|
FMOD
|
[NCBI]
|
5.25922e-05
|
|
|
COL11A1
|
[NCBI]
|
4.53388e-05
|
|
|
BGN
|
[NCBI]
|
4.39706e-05
|
|
|
SLS
|
[NCBI]
|
4.24297e-05
|
|
|
DCN
|
[NCBI]
|
4.22197e-05
|
|
|
RA
|
[NCBI]
|
4.17321e-05
|
|
|
NTRK1
|
[NCBI]
|
3.63584e-05
|
|
|
PAX6
|
[NCBI]
|
3.08867e-05
|
|
|
COL2A1
|
[NCBI]
|
2.82705e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.74198e-05
|
|
|
TNFSF6
|
[NCBI]
|
2.34253e-05
|
|
|
CFTR
|
[NCBI]
|
2.00994e-05
|
|
|
PI
|
[NCBI]
|
1.64324e-05
|
|
|
VEGF
|
[NCBI]
|
1.37079e-05
|
|
|
NGFB
|
[NCBI]
|
8.84082e-06
|
|
|
TNF
|
[NCBI]
|
2.38913e-06
|
|
|
SLE
|
[NCBI]
|
1.39142e-06
|
|
|
PCNA
|
[NCBI]
|
3.39448e-07
|
|
|
EGF
|
[NCBI]
|
2.47195e-07
|
|