|
OMIM |
Link |
Information gain |
01 |
|
HLP
|
[NCBI]
|
0.0099148
|
|
|
porokeratosis of mibelli
|
[NCBI]
|
0.00554583
|
|
|
comedones, familial dyskeratotic
|
[NCBI]
|
0.00208272
|
|
|
keratosis, focal palmoplantar and gingival
|
[NCBI]
|
0.00190818
|
|
|
dyskeratosis, hereditary benign intraepithelial
|
[NCBI]
|
0.00190818
|
|
|
PPPP
|
[NCBI]
|
0.00178424
|
|
|
AKE
|
[NCBI]
|
0.00154007
|
|
|
erythrokeratodermia variabilis 3
|
[NCBI]
|
0.00132134
|
|
|
EKV
|
[NCBI]
|
0.00117515
|
|
|
ichthyosis follicularis, atrichia, and photophobia syndrome
|
[NCBI]
|
0.000966705
|
|
|
ameloonychohypohidrotic syndrome
|
[NCBI]
|
0.000808863
|
|
|
flynn-aird syndrome
|
[NCBI]
|
0.000808863
|
|
|
curly hair-acral keratoderma-caries syndrome
|
[NCBI]
|
0.000808863
|
|
|
DSAP1
|
[NCBI]
|
0.000789677
|
|
|
TOC
|
[NCBI]
|
0.000706229
|
|
|
mucoepithelial dysplasia, hereditary
|
[NCBI]
|
0.000510457
|
|
|
GJB3
|
[NCBI]
|
0.000476234
|
|
|
keratolytic winter erythema
|
[NCBI]
|
0.000457944
|
|
|
keratosis palmoplantaris papulosa
|
[NCBI]
|
0.000388382
|
|
|
sclerotylosis
|
[NCBI]
|
0.000362966
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.00034134
|
|
|
LOR
|
[NCBI]
|
0.000329688
|
|
|
dupuytren contracture
|
[NCBI]
|
0.000305953
|
|
|
dermatitis, atopic
|
[NCBI]
|
0.000305953
|
|
|
PC1
|
[NCBI]
|
0.000298599
|
|
|
AKV
|
[NCBI]
|
0.000288969
|
|
|
BZX
|
[NCBI]
|
0.000277715
|
|
|
knuckle pads, leukonychia, and sensorineural deafness
|
[NCBI]
|
0.000270903
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.000254316
|
|
|
EV
|
[NCBI]
|
0.000244041
|
|
|
DKC
|
[NCBI]
|
0.000224096
|
|
|
RA
|
[NCBI]
|
0.000203165
|
|
|
GJB4
|
[NCBI]
|
0.000200697
|
|
|
EPPK
|
[NCBI]
|
0.000197271
|
|
|
PALS
|
[NCBI]
|
0.000186158
|
|
|
pachyonychia congenita, recessive
|
[NCBI]
|
0.00018586
|
|
|
keratosis pilaris
|
[NCBI]
|
0.00018586
|
|
|
EPS
|
[NCBI]
|
0.000183741
|
|
|
SLE
|
[NCBI]
|
0.000172377
|
|
|
HMS
|
[NCBI]
|
0.000143989
|
|
|
white sponge nevus of cannon
|
[NCBI]
|
0.000132429
|
|
|
kindler syndrome
|
[NCBI]
|
0.000129349
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
0.000126541
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
0.00011533
|
|
|
keratosis follicularis, dwarfism, and cerebral atrophy
|
[NCBI]
|
0.000108325
|
|
|
arthrogryposis with hyperkeratosis
|
[NCBI]
|
0.000108325
|
|
|
acrokeratoderma, hereditary papulotranslucent
|
[NCBI]
|
0.000108325
|
|
|
keratoses, familial actinic
|
[NCBI]
|
0.000108325
|
|
|
keratosis palmaris et plantaris with clinodactyly
|
[NCBI]
|
0.000108325
|
|
|
epithelial squamous dysplasia, keratinizing desquamative, of urinary tract
|
[NCBI]
|
0.000108325
|
|
|
erythrokeratodermia, progressive symmetric
|
[NCBI]
|
0.000108325
|
|
|
porokeratosis plantaris, palmaris, et disseminata
|
[NCBI]
|
0.000108325
|
|
|
seborrheic keratoses
|
[NCBI]
|
0.000108325
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
9.35615e-05
|
|
|
proteus syndrome
|
[NCBI]
|
8.99887e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
8.80341e-05
|
|
|
pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies
|
[NCBI]
|
8.58722e-05
|
|
|
revesz syndrome
|
[NCBI]
|
8.58722e-05
|
|
|
keratosis linearis with ichthyosis congenita and sclerosing keratoderma
|
[NCBI]
|
8.58722e-05
|
|
|
BLK
|
[NCBI]
|
7.78716e-05
|
|
|
carotenemia, familial
|
[NCBI]
|
7.74102e-05
|
|
|
syringomas, multiple
|
[NCBI]
|
7.74102e-05
|
|
|
arthrogryposis and ectodermal dysplasia
|
[NCBI]
|
7.74102e-05
|
|
|
PCNA
|
[NCBI]
|
7.59144e-05
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
7.19221e-05
|
|
|
keratosis palmoplantaris striata i
|
[NCBI]
|
6.46026e-05
|
|
|
vohwinkel syndrome, variant form
|
[NCBI]
|
6.46026e-05
|
|
|
MTMR9
|
[NCBI]
|
6.40948e-05
|
|
|
ichthyosis, bullous type
|
[NCBI]
|
5.96049e-05
|
|
|
IHCM
|
[NCBI]
|
5.75935e-05
|
|
|
mal de meleda
|
[NCBI]
|
5.75935e-05
|
|
|
OCA3
|
[NCBI]
|
5.75935e-05
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
5.58088e-05
|
|
|
monilethrix
|
[NCBI]
|
5.58088e-05
|
|
|
CD
|
[NCBI]
|
5.5037e-05
|
|
|
MANBA
|
[NCBI]
|
5.30155e-05
|
|
|
IP
|
[NCBI]
|
5.02813e-05
|
|
|
GJB2
|
[NCBI]
|
4.95257e-05
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
4.90509e-05
|
|
|
mannosidosis, beta a, lysosomal
|
[NCBI]
|
4.79897e-05
|
|
|
GVM
|
[NCBI]
|
4.79897e-05
|
|
|
tight skin contracture syndrome, lethal
|
[NCBI]
|
4.69961e-05
|
|
|
NETH
|
[NCBI]
|
4.60622e-05
|
|
|
KFSD
|
[NCBI]
|
4.51814e-05
|
|
|
SPINK5
|
[NCBI]
|
4.36983e-05
|
|
|
RHS
|
[NCBI]
|
4.35574e-05
|
|
|
PDP
|
[NCBI]
|
4.35574e-05
|
|
|
KLK7
|
[NCBI]
|
4.28729e-05
|
|
|
DSG2
|
[NCBI]
|
4.28729e-05
|
|
|
DDD
|
[NCBI]
|
4.28054e-05
|
|
|
BGN
|
[NCBI]
|
4.07453e-05
|
|
|
GSTM1
|
[NCBI]
|
4.07453e-05
|
|
|
AEZ
|
[NCBI]
|
4.012e-05
|
|
|
CDSN
|
[NCBI]
|
3.89977e-05
|
|
|
OFD1
|
[NCBI]
|
3.89363e-05
|
|
|
CTSL
|
[NCBI]
|
3.75152e-05
|
|
|
TP73L
|
[NCBI]
|
3.62283e-05
|
|
|
DAR
|
[NCBI]
|
3.58581e-05
|
|
|
PXE
|
[NCBI]
|
3.52559e-05
|
|
|
CDPX2
|
[NCBI]
|
3.45284e-05
|
|
|
FDH
|
[NCBI]
|
3.14776e-05
|
|
|
BCPM
|
[NCBI]
|
3.08054e-05
|
|
|
HMI
|
[NCBI]
|
3.01561e-05
|
|
|
RTS
|
[NCBI]
|
2.81193e-05
|
|
|
B2M
|
[NCBI]
|
2.80466e-05
|
|
|
MTS
|
[NCBI]
|
2.54107e-05
|
|
|
TERT
|
[NCBI]
|
2.46211e-05
|
|
|
ichthyosis, x-linked
|
[NCBI]
|
2.42691e-05
|
|
|
SLS
|
[NCBI]
|
2.25971e-05
|
|
|
KRT20
|
[NCBI]
|
2.08463e-05
|
|
|
GHR
|
[NCBI]
|
2.06891e-05
|
|
|
FGFR2
|
[NCBI]
|
1.97294e-05
|
|
|
SDC2
|
[NCBI]
|
1.8737e-05
|
|
|
CYP1A1
|
[NCBI]
|
1.60644e-05
|
|
|
TP53
|
[NCBI]
|
1.49886e-05
|
|
|
CEACAM5
|
[NCBI]
|
1.27689e-05
|
|
|
BCNS
|
[NCBI]
|
1.22546e-05
|
|
|
EGF
|
[NCBI]
|
1.15395e-05
|
|
|
ALB
|
[NCBI]
|
1.05114e-05
|
|
|
PTK2
|
[NCBI]
|
8.70024e-06
|
|
|
PPARA
|
[NCBI]
|
7.23661e-06
|
|
|
TNFSF6
|
[NCBI]
|
3.76674e-06
|
|
|
G6PD
|
[NCBI]
|
3.18252e-06
|
|
|
CAT
|
[NCBI]
|
2.38737e-06
|
|
|
EGFR
|
[NCBI]
|
1.41829e-06
|
|
|
TS
|
[NCBI]
|
1.16625e-06
|
|
|
PTH
|
[NCBI]
|
1.10109e-06
|
|
|
MPO
|
[NCBI]
|
5.02314e-08
|
|