|
OMIM |
Link |
Information gain |
01 |
|
AKE
|
[NCBI]
|
0.00200421
|
|
|
keratosis, focal palmoplantar and gingival
|
[NCBI]
|
0.00139914
|
|
|
PPPP
|
[NCBI]
|
0.00132809
|
|
|
sclerotylosis
|
[NCBI]
|
0.00127043
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.00111016
|
|
|
HLP
|
[NCBI]
|
0.00108043
|
|
|
pityriasis rubra pilaris
|
[NCBI]
|
0.000742078
|
|
|
CANDN1
|
[NCBI]
|
0.000742078
|
|
|
pigmented purpuric eruption
|
[NCBI]
|
0.000660154
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal recessive
|
[NCBI]
|
0.000607072
|
|
|
keratolytic winter erythema
|
[NCBI]
|
0.000607072
|
|
|
collagenosis, familial reactive perforating
|
[NCBI]
|
0.000567689
|
|
|
candidiasis, familial chronic mucocutaneous, autosomal dominant
|
[NCBI]
|
0.000510391
|
|
|
MSSE
|
[NCBI]
|
0.000488197
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.000488197
|
|
|
TOC
|
[NCBI]
|
0.000386866
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
0.000145963
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
0.000135268
|
|
|
porokeratosis plantaris, palmaris, et disseminata
|
[NCBI]
|
0.000131018
|
|
|
acrokeratoderma, hereditary papulotranslucent
|
[NCBI]
|
0.000131018
|
|
|
peeling skin syndrome, acral type
|
[NCBI]
|
0.000100073
|
|
|
keratosis palmoplantaris striata i
|
[NCBI]
|
8.72191e-05
|
|
|
DPR
|
[NCBI]
|
8.72191e-05
|
|
|
ichthyosis, bullous type
|
[NCBI]
|
8.21907e-05
|
|
|
HMS
|
[NCBI]
|
8.21907e-05
|
|
|
epidermolysis bullosa herpetiformis, dowling-meara type
|
[NCBI]
|
8.0164e-05
|
|
|
DSAP1
|
[NCBI]
|
7.8364e-05
|
|
|
TGM5
|
[NCBI]
|
7.57683e-05
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
7.39269e-05
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
7.15296e-05
|
|
|
kawasaki disease
|
[NCBI]
|
7.0453e-05
|
|
|
EPPK
|
[NCBI]
|
6.94441e-05
|
|
|
ED2
|
[NCBI]
|
6.84949e-05
|
|
|
DDD
|
[NCBI]
|
6.51769e-05
|
|
|
amyloidosis, primary cutaneous
|
[NCBI]
|
6.44447e-05
|
|
|
KRT9
|
[NCBI]
|
6.09492e-05
|
|
|
ICAM1
|
[NCBI]
|
5.56221e-05
|
|
|
DSG1
|
[NCBI]
|
5.2444e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
4.78264e-05
|
|
|
CRMO
|
[NCBI]
|
4.7578e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
4.424e-05
|
|
|
APS1
|
[NCBI]
|
4.01038e-05
|
|
|
CD
|
[NCBI]
|
3.82498e-05
|
|
|
EV
|
[NCBI]
|
3.3961e-05
|
|
|
RA
|
[NCBI]
|
1.53826e-05
|
|
|
CEACAM5
|
[NCBI]
|
7.56857e-06
|
|
|
CRC
|
[NCBI]
|
1.70629e-06
|
|
|
SLE
|
[NCBI]
|
3.80987e-07
|
|