|
OMIM |
Link |
Information gain |
01 |
|
cutis laxa, autosomal dominant
|
[NCBI]
|
0.00010494
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
0.000101892
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
9.93282e-05
|
|
|
CCL22
|
[NCBI]
|
5.35473e-05
|
|
|
TLR2
|
[NCBI]
|
4.48881e-05
|
|
|
SOD2
|
[NCBI]
|
3.4423e-05
|
|
|
SLE
|
[NCBI]
|
2.78841e-05
|
|
|
PCNA
|
[NCBI]
|
1.57012e-05
|
|
|
TNF
|
[NCBI]
|
7.41793e-06
|
|