|
OMIM |
Link |
Information gain |
01 |
|
ameloonychohypohidrotic syndrome
|
[NCBI]
|
0.00129156
|
|
|
spiegler-brooke syndrome
|
[NCBI]
|
0.00078076
|
|
|
schimmelpenning-feuerstein-mims syndrome
|
[NCBI]
|
0.000725612
|
|
|
alopecia, androgenetic
|
[NCBI]
|
0.000306358
|
|
|
perifolliculitis capitis abscedens et suffodiens, familial
|
[NCBI]
|
0.000141395
|
|
|
cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness
|
[NCBI]
|
0.000141395
|
|
|
CVG/MR
|
[NCBI]
|
0.000100846
|
|
|
ichthyosis, bullous type
|
[NCBI]
|
9.25519e-05
|
|
|
complement component 5 deficiency
|
[NCBI]
|
8.70992e-05
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
8.18742e-05
|
|
|
NETH
|
[NCBI]
|
7.88324e-05
|
|
|
CYLD
|
[NCBI]
|
7.88324e-05
|
|
|
KFSD
|
[NCBI]
|
7.79339e-05
|
|
|
PDP
|
[NCBI]
|
7.62745e-05
|
|
|
DSG4
|
[NCBI]
|
7.34161e-05
|
|
|
OFD1
|
[NCBI]
|
7.15296e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
5.18201e-05
|
|
|
ALD
|
[NCBI]
|
2.81442e-05
|
|
|
temporal arteritis
|
[NCBI]
|
2.68225e-05
|
|
|
PCNA
|
[NCBI]
|
1.80307e-05
|
|
|
PTH
|
[NCBI]
|
1.45161e-05
|
|