|
OMIM |
Link |
Information gain |
01 |
|
uncombable hair syndrome
|
[NCBI]
|
0.00319617
|
|
|
woolly hair, autosomal dominant
|
[NCBI]
|
0.00167995
|
|
|
trichorrhexis nodosa syndrome
|
[NCBI]
|
0.00151576
|
|
|
TTDP
|
[NCBI]
|
0.00139995
|
|
|
CHH
|
[NCBI]
|
0.00111712
|
|
|
ERCC2
|
[NCBI]
|
0.000863046
|
|
|
sabinas brittle hair syndrome
|
[NCBI]
|
0.000750767
|
|
|
onychotrichodysplasia and neutropenia
|
[NCBI]
|
0.000697531
|
|
|
acanthosis nigricans
|
[NCBI]
|
0.000626524
|
|
|
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina
|
[NCBI]
|
0.000626524
|
|
|
loose anagen hair syndrome
|
[NCBI]
|
0.00052224
|
|
|
BZX
|
[NCBI]
|
0.00051152
|
|
|
alopecia areata 1
|
[NCBI]
|
0.000465323
|
|
|
monilethrix
|
[NCBI]
|
0.000453758
|
|
|
KRTHB6
|
[NCBI]
|
0.000357252
|
|
|
XPD
|
[NCBI]
|
0.000306768
|
|
|
TTDN1
|
[NCBI]
|
0.000261606
|
|
|
DSG4
|
[NCBI]
|
0.000251794
|
|
|
noonan-like syndrome with loose anagen hair
|
[NCBI]
|
0.000225832
|
|
|
PURE&apos
|
[NCBI]
|
0.000171327
|
|
|
pilomatrixoma
|
[NCBI]
|
0.000163982
|
|
|
BJS
|
[NCBI]
|
0.000163982
|
|
|
KRTHB1
|
[NCBI]
|
0.000158925
|
|
|
naxos disease
|
[NCBI]
|
0.000148656
|
|
|
TTDN1
|
[NCBI]
|
0.000120973
|
|
|
SPINK5
|
[NCBI]
|
0.000105211
|
|
|
ERCC3
|
[NCBI]
|
0.000100415
|
|
|
spondyloepimetaphyseal dysplasia with hypotrichosis
|
[NCBI]
|
9.03621e-05
|
|
|
revesz syndrome
|
[NCBI]
|
9.03621e-05
|
|
|
trichomegaly
|
[NCBI]
|
9.03621e-05
|
|
|
trichodental dysplasia
|
[NCBI]
|
9.03621e-05
|
|
|
uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly
|
[NCBI]
|
9.03621e-05
|
|
|
SLE
|
[NCBI]
|
8.75132e-05
|
|
|
XPA
|
[NCBI]
|
8.34167e-05
|
|
|
nicolaides-baraitser syndrome
|
[NCBI]
|
8.18952e-05
|
|
|
steatocystoma multiplex with natal teeth
|
[NCBI]
|
8.18952e-05
|
|
|
CTNNB1
|
[NCBI]
|
8.16962e-05
|
|
|
KRTHB5
|
[NCBI]
|
7.93609e-05
|
|
|
KLC3
|
[NCBI]
|
7.93609e-05
|
|
|
MPZL3
|
[NCBI]
|
7.93609e-05
|
|
|
keratin 6, hair follicle
|
[NCBI]
|
7.93609e-05
|
|
|
glomerulonephritis with sparse hair and telangiectases
|
[NCBI]
|
7.64022e-05
|
|
|
hypothyroidism, athyroidal, with spiky hair and cleft palate
|
[NCBI]
|
7.23215e-05
|
|
|
AIHHT
|
[NCBI]
|
6.90727e-05
|
|
|
steatocystoma multiplex
|
[NCBI]
|
6.90727e-05
|
|
|
xeroderma pigmentosum, complementation group e
|
[NCBI]
|
6.63736e-05
|
|
|
KRT6B
|
[NCBI]
|
6.55835e-05
|
|
|
XPB
|
[NCBI]
|
6.20489e-05
|
|
|
GTF2H5
|
[NCBI]
|
6.03854e-05
|
|
|
CLDN7
|
[NCBI]
|
6.03854e-05
|
|
|
XPF
|
[NCBI]
|
5.71904e-05
|
|
|
GS2
|
[NCBI]
|
5.71904e-05
|
|
|
KRT6A
|
[NCBI]
|
5.70109e-05
|
|
|
PVALB
|
[NCBI]
|
5.70109e-05
|
|
|
EVC
|
[NCBI]
|
5.45026e-05
|
|
|
AMN
|
[NCBI]
|
5.25043e-05
|
|
|
NCIE1
|
[NCBI]
|
5.24106e-05
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
5.14121e-05
|
|
|
JUP
|
[NCBI]
|
5.08431e-05
|
|
|
NETH
|
[NCBI]
|
5.04733e-05
|
|
|
ED2
|
[NCBI]
|
5.04733e-05
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
5.04733e-05
|
|
|
BCS1L
|
[NCBI]
|
4.94215e-05
|
|
|
RHS
|
[NCBI]
|
4.79537e-05
|
|
|
FOXE1
|
[NCBI]
|
4.70756e-05
|
|
|
TRPS1
|
[NCBI]
|
4.6475e-05
|
|
|
BHD
|
[NCBI]
|
4.6475e-05
|
|
|
ERCC8
|
[NCBI]
|
4.60832e-05
|
|
|
KRT17
|
[NCBI]
|
4.51816e-05
|
|
|
GAN1
|
[NCBI]
|
4.5125e-05
|
|
|
RAB27A
|
[NCBI]
|
4.35935e-05
|
|
|
HR
|
[NCBI]
|
4.22264e-05
|
|
|
GPX1
|
[NCBI]
|
4.22264e-05
|
|
|
OCRL
|
[NCBI]
|
4.01904e-05
|
|
|
EDA
|
[NCBI]
|
3.99571e-05
|
|
|
EVC
|
[NCBI]
|
3.80117e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
3.72213e-05
|
|
|
ERCC5
|
[NCBI]
|
3.69309e-05
|
|
|
XPC
|
[NCBI]
|
3.69309e-05
|
|
|
XPA
|
[NCBI]
|
3.57557e-05
|
|
|
AQP1
|
[NCBI]
|
3.43351e-05
|
|
|
CSA
|
[NCBI]
|
3.31981e-05
|
|
|
RTS
|
[NCBI]
|
3.23432e-05
|
|
|
COL7A1
|
[NCBI]
|
3.18383e-05
|
|
|
WS1
|
[NCBI]
|
3.10215e-05
|
|
|
AMACR
|
[NCBI]
|
3.0996e-05
|
|
|
PAX3
|
[NCBI]
|
2.88386e-05
|
|
|
OCP
|
[NCBI]
|
2.78615e-05
|
|
|
BLM
|
[NCBI]
|
2.76607e-05
|
|
|
WRN
|
[NCBI]
|
2.7075e-05
|
|
|
MPZ
|
[NCBI]
|
2.51515e-05
|
|
|
EGFR
|
[NCBI]
|
1.04167e-05
|
|
|
TS
|
[NCBI]
|
3.04382e-06
|
|
|
APC
|
[NCBI]
|
9.55084e-08
|
|