|
OMIM |
Link |
Information gain |
01 |
|
alopecia, androgenetic
|
[NCBI]
|
0.00908446
|
|
|
gapo syndrome
|
[NCBI]
|
0.00636982
|
|
|
ichthyosis follicularis, atrichia, and photophobia syndrome
|
[NCBI]
|
0.0043106
|
|
|
johnson neuroectodermal syndrome
|
[NCBI]
|
0.00316334
|
|
|
hypotrichosis, marie unna type
|
[NCBI]
|
0.00313163
|
|
|
alopecia-mental retardation syndrome 1
|
[NCBI]
|
0.00236858
|
|
|
mucoepithelial dysplasia, hereditary
|
[NCBI]
|
0.00236858
|
|
|
hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
|
[NCBI]
|
0.00236858
|
|
|
APL
|
[NCBI]
|
0.00230654
|
|
|
CARASIL
|
[NCBI]
|
0.00203669
|
|
|
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality
|
[NCBI]
|
0.00157646
|
|
|
scholte syndrome
|
[NCBI]
|
0.00157646
|
|
|
ALUNC
|
[NCBI]
|
0.00118614
|
|
|
HR
|
[NCBI]
|
0.000960531
|
|
|
alopecia-mental retardation syndrome 2
|
[NCBI]
|
0.000786952
|
|
|
BZX
|
[NCBI]
|
0.000736714
|
|
|
PCOS1
|
[NCBI]
|
0.000719822
|
|
|
alopecia areata 1
|
[NCBI]
|
0.000643117
|
|
|
vitamin d-dependent rickets, type ii
|
[NCBI]
|
0.000607478
|
|
|
VDR
|
[NCBI]
|
0.000542277
|
|
|
vitamin d-dependent rickets, type ii, with normal vitamin d receptor
|
[NCBI]
|
0.000488822
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.000481372
|
|
|
onychotrichodysplasia and neutropenia
|
[NCBI]
|
0.000436447
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.000436447
|
|
|
bullous dystrophy, hereditary macular type
|
[NCBI]
|
0.000436447
|
|
|
alopecia-epilepsy-oligophrenia syndrome of moynahan
|
[NCBI]
|
0.000381725
|
|
|
polyposis, skin pigmentation, alopecia, and fingernail changes
|
[NCBI]
|
0.000381725
|
|
|
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina
|
[NCBI]
|
0.000367161
|
|
|
anosmia, congenital
|
[NCBI]
|
0.000367161
|
|
|
schopf-schulz-passarge syndrome
|
[NCBI]
|
0.000320396
|
|
|
cerebellotrigeminal dermal dysplasia
|
[NCBI]
|
0.000319904
|
|
|
KFSD
|
[NCBI]
|
0.000300431
|
|
|
AR
|
[NCBI]
|
0.000296684
|
|
|
APS2
|
[NCBI]
|
0.000257323
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.0002342
|
|
|
schimmelpenning-feuerstein-mims syndrome
|
[NCBI]
|
0.0002342
|
|
|
loose anagen hair syndrome
|
[NCBI]
|
0.000218912
|
|
|
ACC
|
[NCBI]
|
0.000205789
|
|
|
t-cell immunodeficiency, congenital alopecia, and nail dystrophy
|
[NCBI]
|
0.000190731
|
|
|
alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism
|
[NCBI]
|
0.000159822
|
|
|
satoyoshi syndrome
|
[NCBI]
|
0.000145876
|
|
|
MADA
|
[NCBI]
|
0.000136496
|
|
|
AH
|
[NCBI]
|
0.000136317
|
|
|
IP
|
[NCBI]
|
0.000135314
|
|
|
BJS
|
[NCBI]
|
0.000129002
|
|
|
FOXN1
|
[NCBI]
|
0.000125568
|
|
|
hypotrichosis simplex of scalp
|
[NCBI]
|
0.000123068
|
|
|
SRD5A1
|
[NCBI]
|
0.000111113
|
|
|
monilethrix
|
[NCBI]
|
0.000109974
|
|
|
SLE
|
[NCBI]
|
0.000109429
|
|
|
KRTHB6
|
[NCBI]
|
0.000102947
|
|
|
SFN
|
[NCBI]
|
9.72004e-05
|
|
|
OTD
|
[NCBI]
|
9.53331e-05
|
|
|
alopecia congenita with keratosis palmoplantaris
|
[NCBI]
|
9.53331e-05
|
|
|
hypogonadism, primary, and partial alopecia
|
[NCBI]
|
9.53331e-05
|
|
|
alopecia, familial focal
|
[NCBI]
|
9.53331e-05
|
|
|
CASS
|
[NCBI]
|
9.53331e-05
|
|
|
alopecia universalis congenita, xy gonadal dysgenesis, and laryngomalacia
|
[NCBI]
|
9.53331e-05
|
|
|
alopecia, congenital
|
[NCBI]
|
9.53331e-05
|
|
|
ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features
|
[NCBI]
|
9.53331e-05
|
|
|
parc syndrome
|
[NCBI]
|
9.53331e-05
|
|
|
ichthyosis with alopecia, eclabion, ectropion, and mental retardation
|
[NCBI]
|
9.53331e-05
|
|
|
deafness-craniofacial syndrome
|
[NCBI]
|
9.53331e-05
|
|
|
ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet
|
[NCBI]
|
9.53331e-05
|
|
|
acrocephalopolysyndactyly type iii
|
[NCBI]
|
9.53331e-05
|
|
|
woolly hair, hypotrichosis, everted lower lip, and outstanding ears
|
[NCBI]
|
9.53331e-05
|
|
|
KRT17
|
[NCBI]
|
9.08651e-05
|
|
|
AOS
|
[NCBI]
|
8.98387e-05
|
|
|
ED2
|
[NCBI]
|
8.96663e-05
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
8.96663e-05
|
|
|
holocarboxylase synthetase deficiency
|
[NCBI]
|
8.78562e-05
|
|
|
HGPS
|
[NCBI]
|
8.46291e-05
|
|
|
CTSL
|
[NCBI]
|
7.80578e-05
|
|
|
AEZ
|
[NCBI]
|
7.75131e-05
|
|
|
TERC
|
[NCBI]
|
7.71391e-05
|
|
|
spondyloepimetaphyseal dysplasia with hypotrichosis
|
[NCBI]
|
7.29057e-05
|
|
|
BPH
|
[NCBI]
|
7.29057e-05
|
|
|
ectodermal dysplasia, trichoodontoonychial type
|
[NCBI]
|
7.29057e-05
|
|
|
aplasia cutis congenita, high myopia, and cone-rod dysfunction
|
[NCBI]
|
7.29057e-05
|
|
|
noonan-like syndrome with loose anagen hair
|
[NCBI]
|
7.29057e-05
|
|
|
KRTHB3
|
[NCBI]
|
7.22225e-05
|
|
|
COL17A1
|
[NCBI]
|
7.10245e-05
|
|
|
CYP17A1
|
[NCBI]
|
6.85626e-05
|
|
|
ODDD
|
[NCBI]
|
6.70507e-05
|
|
|
CDPX2
|
[NCBI]
|
6.61822e-05
|
|
|
alopecia-contractures-dwarfism mental retardation syndrome
|
[NCBI]
|
6.44687e-05
|
|
|
syringomas, multiple
|
[NCBI]
|
6.44687e-05
|
|
|
multiple pterygium syndrome, aslan type
|
[NCBI]
|
6.44687e-05
|
|
|
epidermolysis bullosa, late-onset localized junctional, with mental retardation
|
[NCBI]
|
5.90056e-05
|
|
|
HJMD
|
[NCBI]
|
5.90056e-05
|
|
|
eem syndrome
|
[NCBI]
|
5.90056e-05
|
|
|
glomerulonephritis with sparse hair and telangiectases
|
[NCBI]
|
5.90056e-05
|
|
|
PURE&apos
|
[NCBI]
|
5.49549e-05
|
|
|
EPHB3
|
[NCBI]
|
5.32541e-05
|
|
|
chromosome 18p deletion syndrome
|
[NCBI]
|
5.17361e-05
|
|
|
aplasia cutis congenita with epibulbar dermoids
|
[NCBI]
|
5.17361e-05
|
|
|
DPR
|
[NCBI]
|
5.17361e-05
|
|
|
CHRD
|
[NCBI]
|
4.98832e-05
|
|
|
PTPN6
|
[NCBI]
|
4.98832e-05
|
|
|
SHH
|
[NCBI]
|
4.94039e-05
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
4.90669e-05
|
|
|
CLCN2
|
[NCBI]
|
4.53837e-05
|
|
|
SLC39A4
|
[NCBI]
|
4.37261e-05
|
|
|
RXRA
|
[NCBI]
|
4.37261e-05
|
|
|
sc phocomelia syndrome
|
[NCBI]
|
4.14638e-05
|
|
|
FPRL1
|
[NCBI]
|
3.99692e-05
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
3.87261e-05
|
|
|
mast cell disease
|
[NCBI]
|
3.75231e-05
|
|
|
XPD
|
[NCBI]
|
3.53732e-05
|
|
|
GVM
|
[NCBI]
|
3.53732e-05
|
|
|
GAD2
|
[NCBI]
|
3.39485e-05
|
|
|
IL1RN
|
[NCBI]
|
3.39485e-05
|
|
|
CDSN
|
[NCBI]
|
3.34029e-05
|
|
|
GJB6
|
[NCBI]
|
3.28864e-05
|
|
|
EDA
|
[NCBI]
|
3.28864e-05
|
|
|
NOTCH1
|
[NCBI]
|
3.2396e-05
|
|
|
TTDP
|
[NCBI]
|
3.18316e-05
|
|
|
CDKN1A
|
[NCBI]
|
3.14843e-05
|
|
|
SRD5A2
|
[NCBI]
|
3.14843e-05
|
|
|
ERCC2
|
[NCBI]
|
2.98852e-05
|
|
|
GABEB
|
[NCBI]
|
2.96472e-05
|
|
|
TRPS1
|
[NCBI]
|
2.96472e-05
|
|
|
SCD
|
[NCBI]
|
2.91757e-05
|
|
|
HSS
|
[NCBI]
|
2.89874e-05
|
|
|
VEGF
|
[NCBI]
|
2.79074e-05
|
|
|
biotinidase deficiency
|
[NCBI]
|
2.662e-05
|
|
|
POLG
|
[NCBI]
|
2.6255e-05
|
|
|
HDAC1
|
[NCBI]
|
2.6007e-05
|
|
|
PPSH
|
[NCBI]
|
2.45994e-05
|
|
|
CRC
|
[NCBI]
|
2.38725e-05
|
|
|
RCDP1
|
[NCBI]
|
2.24372e-05
|
|
|
DKC
|
[NCBI]
|
2.12925e-05
|
|
|
obesity
|
[NCBI]
|
2.02415e-05
|
|
|
FDH
|
[NCBI]
|
1.95866e-05
|
|
|
AIRE
|
[NCBI]
|
1.88703e-05
|
|
|
PPARG
|
[NCBI]
|
1.88703e-05
|
|
|
ED1
|
[NCBI]
|
1.70079e-05
|
|
|
CDK2
|
[NCBI]
|
1.67856e-05
|
|
|
ATM
|
[NCBI]
|
1.64399e-05
|
|
|
prostate cancer
|
[NCBI]
|
1.55564e-05
|
|
|
SHBG
|
[NCBI]
|
1.4836e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
1.46827e-05
|
|
|
hypertension, essential
|
[NCBI]
|
1.44747e-05
|
|
|
CHH
|
[NCBI]
|
1.31213e-05
|
|
|
FGF7
|
[NCBI]
|
1.00529e-05
|
|
|
EGF
|
[NCBI]
|
9.18138e-06
|
|
|
APS1
|
[NCBI]
|
8.57434e-06
|
|
|
CEACAM5
|
[NCBI]
|
8.16757e-06
|
|
|
SMAX1
|
[NCBI]
|
4.95548e-06
|
|
|
AIS
|
[NCBI]
|
3.18307e-06
|
|
|
PRL
|
[NCBI]
|
2.73037e-06
|
|
|
EPO
|
[NCBI]
|
1.26704e-06
|
|
|
PTH
|
[NCBI]
|
1.03828e-06
|
|
|
ALD
|
[NCBI]
|
2.6693e-07
|
|
|
AT
|
[NCBI]
|
5.06221e-08
|
|
|
KLK3
|
[NCBI]
|
2.64027e-08
|
|