|
OMIM |
Link |
Information gain |
01 |
|
ichthyosis, x-linked
|
[NCBI]
|
0.00351178
|
|
|
ichthyosis follicularis, atrichia, and photophobia syndrome
|
[NCBI]
|
0.00328602
|
|
|
ichthyosis prematurity syndrome
|
[NCBI]
|
0.0030116
|
|
|
SLS
|
[NCBI]
|
0.00177644
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
0.00123763
|
|
|
exfoliative ichthyosis, autosomal recessive, ichthyosis bullosa of siemens-like
|
[NCBI]
|
0.000993831
|
|
|
LI1
|
[NCBI]
|
0.000992506
|
|
|
NLS
|
[NCBI]
|
0.000895081
|
|
|
ichthyosis congenita, harlequin fetus type
|
[NCBI]
|
0.000857135
|
|
|
NCIE1
|
[NCBI]
|
0.00082126
|
|
|
ichthyosis, bullous type
|
[NCBI]
|
0.000793446
|
|
|
NETH
|
[NCBI]
|
0.00079247
|
|
|
NNCI
|
[NCBI]
|
0.000776146
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
0.000729562
|
|
|
NCR
|
[NCBI]
|
0.000694153
|
|
|
LI5
|
[NCBI]
|
0.000694153
|
|
|
sabinas brittle hair syndrome
|
[NCBI]
|
0.000694153
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
0.000693975
|
|
|
woolly hair, autosomal dominant
|
[NCBI]
|
0.000641003
|
|
|
CDS
|
[NCBI]
|
0.000625687
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
0.000618151
|
|
|
IHCM
|
[NCBI]
|
0.000616764
|
|
|
zunich neuroectodermal syndrome
|
[NCBI]
|
0.000594588
|
|
|
trichorrhexis nodosa syndrome
|
[NCBI]
|
0.000570168
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.000521852
|
|
|
TTDP
|
[NCBI]
|
0.000484523
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
0.000449387
|
|
|
KRT2A
|
[NCBI]
|
0.000437089
|
|
|
ichthyosis, lamellar, autosomal dominant
|
[NCBI]
|
0.00035554
|
|
|
EKV
|
[NCBI]
|
0.000345176
|
|
|
vohwinkel syndrome, variant form
|
[NCBI]
|
0.000334225
|
|
|
TGM1
|
[NCBI]
|
0.000301636
|
|
|
SLE
|
[NCBI]
|
0.000298752
|
|
|
ichthyosis--cheek--eyebrow syndrome
|
[NCBI]
|
0.000296925
|
|
|
ichthyosis hystrix gravior
|
[NCBI]
|
0.000296925
|
|
|
ichthyosis and male hypogonadism
|
[NCBI]
|
0.000296925
|
|
|
ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
|
[NCBI]
|
0.000296925
|
|
|
gaucher disease, perinatal lethal
|
[NCBI]
|
0.00027943
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.000255266
|
|
|
keratosis linearis with ichthyosis congenita and sclerosing keratoderma
|
[NCBI]
|
0.000197868
|
|
|
ichthyosis, hystrix-like, with deafness
|
[NCBI]
|
0.000197868
|
|
|
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis
|
[NCBI]
|
0.000197868
|
|
|
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
[NCBI]
|
0.000179402
|
|
|
CDPX1
|
[NCBI]
|
0.000163161
|
|
|
CLDN1
|
[NCBI]
|
0.000160242
|
|
|
FLG
|
[NCBI]
|
0.000148805
|
|
|
SPINK5
|
[NCBI]
|
0.000145805
|
|
|
GJB2
|
[NCBI]
|
0.000134831
|
|
|
MSD
|
[NCBI]
|
0.000133552
|
|
|
LBR
|
[NCBI]
|
0.00013056
|
|
|
TTDN1
|
[NCBI]
|
0.00013016
|
|
|
CDPX2
|
[NCBI]
|
0.000129363
|
|
|
TTDN1
|
[NCBI]
|
0.000103857
|
|
|
XPD
|
[NCBI]
|
0.000100651
|
|
|
ST14
|
[NCBI]
|
0.000100199
|
|
|
ichthyosis, hepatosplenomegaly, and cerebellar degeneration
|
[NCBI]
|
9.88934e-05
|
|
|
camptodactyly-ichthyosis syndrome
|
[NCBI]
|
9.88934e-05
|
|
|
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
|
[NCBI]
|
9.88934e-05
|
|
|
oral and digital anomalies with ichthyosis
|
[NCBI]
|
9.88934e-05
|
|
|
trichodysplasia-xeroderma
|
[NCBI]
|
9.88934e-05
|
|
|
ichthyosis with alopecia, eclabion, ectropion, and mental retardation
|
[NCBI]
|
9.88934e-05
|
|
|
osteosclerosis with ichthyosis and fractures
|
[NCBI]
|
9.88934e-05
|
|
|
ichthyosis, split hairs, and amino aciduria
|
[NCBI]
|
9.88934e-05
|
|
|
ichthyosis with hypotrichosis, autosomal recessive
|
[NCBI]
|
9.88934e-05
|
|
|
ichthyosis, mental retardation, dwarfism, and renal impairment
|
[NCBI]
|
9.88934e-05
|
|
|
stormorken syndrome
|
[NCBI]
|
9.88934e-05
|
|
|
ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin
|
[NCBI]
|
9.88934e-05
|
|
|
PHA
|
[NCBI]
|
8.44351e-05
|
|
|
GBA
|
[NCBI]
|
8.40922e-05
|
|
|
KRT1
|
[NCBI]
|
8.06978e-05
|
|
|
sjogren-larsson-like ichthyosis without cns or eye involvement
|
[NCBI]
|
7.6457e-05
|
|
|
GJB3
|
[NCBI]
|
7.35312e-05
|
|
|
ERCC2
|
[NCBI]
|
7.1116e-05
|
|
|
ARSC2
|
[NCBI]
|
7.08523e-05
|
|
|
RPL12
|
[NCBI]
|
7.08523e-05
|
|
|
SNAP29
|
[NCBI]
|
7.08523e-05
|
|
|
ZNF79
|
[NCBI]
|
7.08523e-05
|
|
|
arthrogryposis and ectodermal dysplasia
|
[NCBI]
|
6.80112e-05
|
|
|
ALDH3A2
|
[NCBI]
|
6.52749e-05
|
|
|
OA1
|
[NCBI]
|
6.36632e-05
|
|
|
LI3
|
[NCBI]
|
6.25391e-05
|
|
|
keratitis, hereditary
|
[NCBI]
|
5.84794e-05
|
|
|
KAL1
|
[NCBI]
|
5.83006e-05
|
|
|
ichthyin
|
[NCBI]
|
5.70795e-05
|
|
|
SLC2A8
|
[NCBI]
|
5.70795e-05
|
|
|
ANGPTL2
|
[NCBI]
|
5.70795e-05
|
|
|
keratosis palmoplantaris striata i
|
[NCBI]
|
5.52517e-05
|
|
|
GTF2H1
|
[NCBI]
|
5.1886e-05
|
|
|
keratoderma, palmoplantar, with deafness
|
[NCBI]
|
5.02861e-05
|
|
|
STXBP1
|
[NCBI]
|
4.85161e-05
|
|
|
CD99
|
[NCBI]
|
4.85161e-05
|
|
|
epidermolysis bullosa dystrophica, pasini type
|
[NCBI]
|
4.49346e-05
|
|
|
hyperprolinemia, type i
|
[NCBI]
|
4.2179e-05
|
|
|
gaucher disease, type ii
|
[NCBI]
|
3.98445e-05
|
|
|
XG
|
[NCBI]
|
3.97072e-05
|
|
|
LOR
|
[NCBI]
|
3.97072e-05
|
|
|
KEAP1
|
[NCBI]
|
3.97072e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
3.87993e-05
|
|
|
muckle-wells syndrome
|
[NCBI]
|
3.87993e-05
|
|
|
EPPK
|
[NCBI]
|
3.78218e-05
|
|
|
ED2
|
[NCBI]
|
3.6904e-05
|
|
|
LMX1B
|
[NCBI]
|
3.59021e-05
|
|
|
KLK7
|
[NCBI]
|
3.59021e-05
|
|
|
ERCC3
|
[NCBI]
|
3.4442e-05
|
|
|
BGN
|
[NCBI]
|
3.37867e-05
|
|
|
histidinemia
|
[NCBI]
|
3.05029e-05
|
|
|
epidermolysis bullosa letalis
|
[NCBI]
|
2.93959e-05
|
|
|
EBR1
|
[NCBI]
|
2.88731e-05
|
|
|
DAZ
|
[NCBI]
|
2.65604e-05
|
|
|
RCDP1
|
[NCBI]
|
2.56754e-05
|
|
|
mannosidosis, alpha b, lysosomal
|
[NCBI]
|
2.56754e-05
|
|
|
FDH
|
[NCBI]
|
2.27531e-05
|
|
|
HEMB
|
[NCBI]
|
1.0885e-05
|
|
|
PTH
|
[NCBI]
|
9.86853e-06
|
|
|
EGFR
|
[NCBI]
|
7.23185e-06
|
|
|
EV
|
[NCBI]
|
6.64043e-06
|
|
|
DMD
|
[NCBI]
|
4.73431e-06
|
|
|
DHFR
|
[NCBI]
|
3.12914e-06
|
|
|
AFP
|
[NCBI]
|
2.51137e-06
|
|
|
ADA
|
[NCBI]
|
7.84432e-07
|
|