|
OMIM |
Link |
Information gain |
01 |
|
trichorrhexis nodosa syndrome
|
[NCBI]
|
0.00459302
|
|
|
onychotrichodysplasia and neutropenia
|
[NCBI]
|
0.00415073
|
|
|
trichohepatoenteric syndrome
|
[NCBI]
|
0.00415073
|
|
|
uncombable hair syndrome
|
[NCBI]
|
0.00415073
|
|
|
woolly hair, autosomal dominant
|
[NCBI]
|
0.00415073
|
|
|
BZX
|
[NCBI]
|
0.00350976
|
|
|
alopecia, androgenetic
|
[NCBI]
|
0.00318265
|
|
|
CHH
|
[NCBI]
|
0.00315936
|
|
|
sabinas brittle hair syndrome
|
[NCBI]
|
0.00310773
|
|
|
zinc, elevated plasma
|
[NCBI]
|
0.00206831
|
|
|
menkes disease
|
[NCBI]
|
0.00134355
|
|
|
monilethrix
|
[NCBI]
|
0.00133374
|
|
|
NETH
|
[NCBI]
|
0.00132609
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
0.00132609
|
|
|
RA
|
[NCBI]
|
0.00118062
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.00115339
|
|
|
hypotrichosis, marie unna type
|
[NCBI]
|
0.00113988
|
|
|
TRPS1
|
[NCBI]
|
0.00112291
|
|
|
cranioectodermal dysplasia
|
[NCBI]
|
0.00107237
|
|
|
MRXS12
|
[NCBI]
|
0.00103242
|
|
|
ameloonychohypohidrotic syndrome
|
[NCBI]
|
0.00103242
|
|
|
pseudomonilethrix
|
[NCBI]
|
0.00103242
|
|
|
ringed hair
|
[NCBI]
|
0.00103242
|
|
|
midphalangeal hair
|
[NCBI]
|
0.00103242
|
|
|
book syndrome
|
[NCBI]
|
0.00103242
|
|
|
flynn-aird syndrome
|
[NCBI]
|
0.00103242
|
|
|
rosselli-gulienetti syndrome
|
[NCBI]
|
0.00103242
|
|
|
curly hair-acral keratoderma-caries syndrome
|
[NCBI]
|
0.00103242
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.000918186
|
|
|
TTDN1
|
[NCBI]
|
0.000856071
|
|
|
TTDP
|
[NCBI]
|
0.000849752
|
|
|
alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality
|
[NCBI]
|
0.000723672
|
|
|
dilution, pigmentary
|
[NCBI]
|
0.000723672
|
|
|
acanthosis nigricans
|
[NCBI]
|
0.000723672
|
|
|
TRICY1
|
[NCBI]
|
0.000723672
|
|
|
hypertrichosis universalis
|
[NCBI]
|
0.000608534
|
|
|
brachydactyly-mental retardation syndrome
|
[NCBI]
|
0.000534551
|
|
|
focal facial dermal dysplasia
|
[NCBI]
|
0.000534551
|
|
|
VRNI
|
[NCBI]
|
0.00051915
|
|
|
SLE
|
[NCBI]
|
0.000519003
|
|
|
loose anagen hair syndrome
|
[NCBI]
|
0.000499669
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
0.000485161
|
|
|
CF
|
[NCBI]
|
0.000481187
|
|
|
syndactyly, type i, with microcephaly and mental retardation
|
[NCBI]
|
0.000480113
|
|
|
DA5
|
[NCBI]
|
0.000480113
|
|
|
chromosome 10q deletion syndrome
|
[NCBI]
|
0.000480113
|
|
|
TRPS2
|
[NCBI]
|
0.000479532
|
|
|
hypotrichosis simplex of scalp
|
[NCBI]
|
0.000462538
|
|
|
blepharocheilodontic syndrome
|
[NCBI]
|
0.000437188
|
|
|
costello syndrome
|
[NCBI]
|
0.000435136
|
|
|
KRTHA1
|
[NCBI]
|
0.000433503
|
|
|
OCA1B
|
[NCBI]
|
0.000427653
|
|
|
spiegler-brooke syndrome
|
[NCBI]
|
0.00040187
|
|
|
peeling skin syndrome
|
[NCBI]
|
0.00040187
|
|
|
PURE&apos
|
[NCBI]
|
0.000364108
|
|
|
OCA1A
|
[NCBI]
|
0.000362412
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.00034609
|
|
|
kabuki syndrome
|
[NCBI]
|
0.000344572
|
|
|
BJS
|
[NCBI]
|
0.000332682
|
|
|
elejalde disease
|
[NCBI]
|
0.000310375
|
|
|
GPHN
|
[NCBI]
|
0.000285017
|
|
|
trichodiscomas, familial multiple
|
[NCBI]
|
0.000285017
|
|
|
noonan-like syndrome with loose anagen hair
|
[NCBI]
|
0.000285017
|
|
|
arthrogryposis and ectodermal dysplasia
|
[NCBI]
|
0.000285017
|
|
|
trichodental dysplasia
|
[NCBI]
|
0.000285017
|
|
|
teebi-shaltout syndrome
|
[NCBI]
|
0.000285017
|
|
|
ED1
|
[NCBI]
|
0.000269626
|
|
|
RHS
|
[NCBI]
|
0.000266455
|
|
|
GAN1
|
[NCBI]
|
0.000262819
|
|
|
KRTHB6
|
[NCBI]
|
0.000240546
|
|
|
MCKD1
|
[NCBI]
|
0.000239679
|
|
|
ERCC2
|
[NCBI]
|
0.000232784
|
|
|
nicolaides-baraitser syndrome
|
[NCBI]
|
0.0002311
|
|
|
naxos disease
|
[NCBI]
|
0.0002311
|
|
|
ED3
|
[NCBI]
|
0.0002311
|
|
|
metaphyseal dysplasia without hypotrichosis
|
[NCBI]
|
0.0002311
|
|
|
ED2
|
[NCBI]
|
0.000230531
|
|
|
KRTHA2
|
[NCBI]
|
0.000221087
|
|
|
hair whorl
|
[NCBI]
|
0.000206833
|
|
|
SHEP2
|
[NCBI]
|
0.000206833
|
|
|
AIHHT
|
[NCBI]
|
0.000206833
|
|
|
witkop syndrome
|
[NCBI]
|
0.000206833
|
|
|
hairy ears
|
[NCBI]
|
0.000206833
|
|
|
DSG4
|
[NCBI]
|
0.000196057
|
|
|
KRTHB1
|
[NCBI]
|
0.00019238
|
|
|
hypothyroidism, athyroidal, with spiky hair and cleft palate
|
[NCBI]
|
0.000190233
|
|
|
TRPS3
|
[NCBI]
|
0.000190233
|
|
|
RMRP
|
[NCBI]
|
0.000181913
|
|
|
cardiomyopathy, dilated, with woolly hair and keratoderma
|
[NCBI]
|
0.000177554
|
|
|
hairy ears, y-linked
|
[NCBI]
|
0.000177554
|
|
|
KRN1
|
[NCBI]
|
0.00017437
|
|
|
GS1
|
[NCBI]
|
0.00016729
|
|
|
TTDN1
|
[NCBI]
|
0.000164894
|
|
|
GS2
|
[NCBI]
|
0.00015867
|
|
|
XPD
|
[NCBI]
|
0.000144723
|
|
|
KRTHA3A
|
[NCBI]
|
0.000144242
|
|
|
KRTHA6
|
[NCBI]
|
0.000144242
|
|
|
KRTHA4
|
[NCBI]
|
0.000144242
|
|
|
ectodermal dysplasia, hidrotic, autosomal recessive
|
[NCBI]
|
0.000142466
|
|
|
pilodental dysplasia with refractive errors
|
[NCBI]
|
0.000142466
|
|
|
dermoodontodysplasia
|
[NCBI]
|
0.000142466
|
|
|
osteopenia and sparse hair
|
[NCBI]
|
0.000142466
|
|
|
thumb deformity and alopecia
|
[NCBI]
|
0.000142466
|
|
|
alopecia, familial focal
|
[NCBI]
|
0.000142466
|
|
|
ectodermal dysplasia, hidrotic, christianson-fourie type
|
[NCBI]
|
0.000142466
|
|
|
piebald trait with neurologic defects
|
[NCBI]
|
0.000142466
|
|
|
crumpled helices and small mouth
|
[NCBI]
|
0.000142466
|
|
|
xanthinuria, type ii
|
[NCBI]
|
0.000142466
|
|
|
cyanide, inability to smell
|
[NCBI]
|
0.000142466
|
|
|
parc syndrome
|
[NCBI]
|
0.000142466
|
|
|
ichthyosis, split hairs, and amino aciduria
|
[NCBI]
|
0.000142466
|
|
|
anonychia with flexural pigmentation
|
[NCBI]
|
0.000142466
|
|
|
ectodermal dysplasia with natal teeth, turnpenny type
|
[NCBI]
|
0.000142466
|
|
|
monilethrix
|
[NCBI]
|
0.000142466
|
|
|
spinocerebellar ataxia with dysmorphism
|
[NCBI]
|
0.000142466
|
|
|
odontotrichoungual-digital-palmar syndrome
|
[NCBI]
|
0.000142466
|
|
|
pili torti and developmental delay
|
[NCBI]
|
0.000142466
|
|
|
hairy nose tip
|
[NCBI]
|
0.000142466
|
|
|
alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism
|
[NCBI]
|
0.000142466
|
|
|
incisors, lower central, absence of
|
[NCBI]
|
0.000142466
|
|
|
alopecia-epilepsy-oligophrenia syndrome of moynahan
|
[NCBI]
|
0.000142466
|
|
|
skin fragility-woolly hair syndrome
|
[NCBI]
|
0.000142466
|
|
|
MOTA
|
[NCBI]
|
0.000142466
|
|
|
trichodysplasia-xeroderma
|
[NCBI]
|
0.000142466
|
|
|
trichoepitheliomas, multiple desmoplastic
|
[NCBI]
|
0.000142466
|
|
|
woolly hair, autosomal recessive
|
[NCBI]
|
0.000142466
|
|
|
woolly hair, hypotrichosis, everted lower lip, and outstanding ears
|
[NCBI]
|
0.000142466
|
|
|
partington-anderson syndrome
|
[NCBI]
|
0.000142466
|
|
|
BHD
|
[NCBI]
|
0.000128926
|
|
|
EEC1
|
[NCBI]
|
0.000125331
|
|
|
MC1R
|
[NCBI]
|
0.000121712
|
|
|
ichthyosis congenita, harlequin fetus type
|
[NCBI]
|
0.000120545
|
|
|
DLX3
|
[NCBI]
|
0.000114318
|
|
|
poland syndrome
|
[NCBI]
|
0.000108863
|
|
|
SMMCI
|
[NCBI]
|
0.000107027
|
|
|
nevus, keratinocytic, nonepidermolytic
|
[NCBI]
|
0.000103375
|
|
|
chands
|
[NCBI]
|
0.000103375
|
|
|
ichthyosis hystrix gravior
|
[NCBI]
|
0.000103375
|
|
|
pernicious anemia
|
[NCBI]
|
0.000103375
|
|
|
ectodermal dysplasia, trichoodontoonychial type
|
[NCBI]
|
0.000103375
|
|
|
GS3
|
[NCBI]
|
0.000103375
|
|
|
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
|
[NCBI]
|
0.000103375
|
|
|
ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis
|
[NCBI]
|
0.000103375
|
|
|
uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly
|
[NCBI]
|
0.000103375
|
|
|
FGF5
|
[NCBI]
|
0.00010304
|
|
|
EV
|
[NCBI]
|
9.94687e-05
|
|
|
KRTHA8
|
[NCBI]
|
9.61328e-05
|
|
|
KRTHA7
|
[NCBI]
|
9.61328e-05
|
|
|
KRTHA3B
|
[NCBI]
|
9.61328e-05
|
|
|
CFNS
|
[NCBI]
|
9.40524e-05
|
|
|
ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia
|
[NCBI]
|
8.87359e-05
|
|
|
EDA
|
[NCBI]
|
8.47054e-05
|
|
|
KRTHA5
|
[NCBI]
|
8.23899e-05
|
|
|
mucopolysaccharidosis type ii
|
[NCBI]
|
8.0944e-05
|
|
|
AH
|
[NCBI]
|
7.92945e-05
|
|
|
SHH
|
[NCBI]
|
7.82073e-05
|
|
|
scalp-ear-nipple syndrome
|
[NCBI]
|
7.23215e-05
|
|
|
CLPED1
|
[NCBI]
|
7.23215e-05
|
|
|
WS1
|
[NCBI]
|
6.96977e-05
|
|
|
ruvalcaba syndrome
|
[NCBI]
|
6.68025e-05
|
|
|
ankyloblepharon-ectodermal defects-cleft lip/palate
|
[NCBI]
|
6.68025e-05
|
|
|
xanthinuria, type i
|
[NCBI]
|
6.68025e-05
|
|
|
BDE
|
[NCBI]
|
6.68025e-05
|
|
|
MCDS
|
[NCBI]
|
6.68025e-05
|
|
|
SHBG
|
[NCBI]
|
6.2791e-05
|
|
|
ALUNC
|
[NCBI]
|
6.22443e-05
|
|
|
SPINK5
|
[NCBI]
|
6.01679e-05
|
|
|
NS1
|
[NCBI]
|
5.90274e-05
|
|
|
TYR
|
[NCBI]
|
5.89779e-05
|
|
|
DKK1
|
[NCBI]
|
5.86537e-05
|
|
|
ablepharon-macrostomia syndrome
|
[NCBI]
|
5.83688e-05
|
|
|
KRT1
|
[NCBI]
|
5.60384e-05
|
|
|
AIS
|
[NCBI]
|
5.51306e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
5.50039e-05
|
|
|
LEF1
|
[NCBI]
|
5.38318e-05
|
|
|
diabetes-deafness syndrome, maternally transmitted
|
[NCBI]
|
5.20352e-05
|
|
|
VEGF
|
[NCBI]
|
4.983e-05
|
|
|
HPRT1
|
[NCBI]
|
4.8722e-05
|
|
|
hairy palms and soles
|
[NCBI]
|
4.80522e-05
|
|
|
KLC3
|
[NCBI]
|
4.80522e-05
|
|
|
KRTHB3
|
[NCBI]
|
4.80522e-05
|
|
|
KRN1L
|
[NCBI]
|
4.80522e-05
|
|
|
KRTHB4
|
[NCBI]
|
4.80522e-05
|
|
|
hair follicle-specific gene 1
|
[NCBI]
|
4.80522e-05
|
|
|
KRTAP13-1
|
[NCBI]
|
4.80522e-05
|
|
|
diabetes mellitus, insulin-resistant, with acanthosis nigricans
|
[NCBI]
|
4.69898e-05
|
|
|
NCIE1
|
[NCBI]
|
4.69898e-05
|
|
|
kniest dysplasia
|
[NCBI]
|
4.69898e-05
|
|
|
ALDH2
|
[NCBI]
|
4.50156e-05
|
|
|
chromosome 18q deletion syndrome
|
[NCBI]
|
4.4812e-05
|
|
|
argininosuccinic aciduria
|
[NCBI]
|
4.4812e-05
|
|
|
FGF7
|
[NCBI]
|
4.4039e-05
|
|
|
ALDH1A1
|
[NCBI]
|
4.39659e-05
|
|
|
PRL
|
[NCBI]
|
4.30764e-05
|
|
|
weaver syndrome
|
[NCBI]
|
4.28163e-05
|
|
|
OCA2
|
[NCBI]
|
4.28163e-05
|
|
|
tight skin contracture syndrome, lethal
|
[NCBI]
|
4.28163e-05
|
|
|
CYP1A1
|
[NCBI]
|
4.17916e-05
|
|
|
AEZ
|
[NCBI]
|
4.09768e-05
|
|
|
heterotopia, periventricular, x-linked dominant
|
[NCBI]
|
4.09768e-05
|
|
|
CDPX1
|
[NCBI]
|
3.92725e-05
|
|
|
KRTAP1-3
|
[NCBI]
|
3.80776e-05
|
|
|
HOXC13
|
[NCBI]
|
3.80776e-05
|
|
|
KRTHB5
|
[NCBI]
|
3.80776e-05
|
|
|
KRTAP1-4
|
[NCBI]
|
3.80776e-05
|
|
|
KRTAP1-1
|
[NCBI]
|
3.80776e-05
|
|
|
KRTAP1-5
|
[NCBI]
|
3.80776e-05
|
|
|
FZD6
|
[NCBI]
|
3.80776e-05
|
|
|
ALOX15B
|
[NCBI]
|
3.80776e-05
|
|
|
GABEB
|
[NCBI]
|
3.76865e-05
|
|
|
KFSD
|
[NCBI]
|
3.76865e-05
|
|
|
DSG3
|
[NCBI]
|
3.72843e-05
|
|
|
cutis laxa, x-linked
|
[NCBI]
|
3.4816e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
3.4816e-05
|
|
|
fabry disease
|
[NCBI]
|
3.45032e-05
|
|
|
ALDH7A1
|
[NCBI]
|
3.43184e-05
|
|
|
TNFRSF19
|
[NCBI]
|
3.43184e-05
|
|
|
ELOVL3
|
[NCBI]
|
3.43184e-05
|
|
|
AR
|
[NCBI]
|
3.40374e-05
|
|
|
JBS
|
[NCBI]
|
3.35101e-05
|
|
|
OFD1
|
[NCBI]
|
3.22789e-05
|
|
|
LIPH
|
[NCBI]
|
3.18804e-05
|
|
|
MTTW
|
[NCBI]
|
3.18804e-05
|
|
|
EPIM
|
[NCBI]
|
3.00699e-05
|
|
|
MAP3K13
|
[NCBI]
|
3.00699e-05
|
|
|
BNC1
|
[NCBI]
|
3.00699e-05
|
|
|
SENP2
|
[NCBI]
|
3.00699e-05
|
|
|
SLC27A4
|
[NCBI]
|
3.00699e-05
|
|
|
CHS
|
[NCBI]
|
2.99153e-05
|
|
|
ODDD
|
[NCBI]
|
2.89666e-05
|
|
|
LTB
|
[NCBI]
|
2.86289e-05
|
|
|
IL11RA
|
[NCBI]
|
2.86289e-05
|
|
|
PRLR
|
[NCBI]
|
2.83264e-05
|
|
|
OKS
|
[NCBI]
|
2.79717e-05
|
|
|
LHX2
|
[NCBI]
|
2.74321e-05
|
|
|
KRT17
|
[NCBI]
|
2.74321e-05
|
|
|
EDAR
|
[NCBI]
|
2.74321e-05
|
|
|
SAT1
|
[NCBI]
|
2.74321e-05
|
|
|
GAN
|
[NCBI]
|
2.74321e-05
|
|
|
AMN
|
[NCBI]
|
2.74321e-05
|
|
|
FOXN1
|
[NCBI]
|
2.64088e-05
|
|
|
TLN1
|
[NCBI]
|
2.64088e-05
|
|
|
TRPS1
|
[NCBI]
|
2.64088e-05
|
|
|
DVL2
|
[NCBI]
|
2.64088e-05
|
|
|
MLPH
|
[NCBI]
|
2.64088e-05
|
|
|
TDGF1
|
[NCBI]
|
2.64088e-05
|
|
|
BCS1L
|
[NCBI]
|
2.64088e-05
|
|
|
PD
|
[NCBI]
|
2.62925e-05
|
|
|
CDG1A
|
[NCBI]
|
2.61201e-05
|
|
|
GTF2H1
|
[NCBI]
|
2.55154e-05
|
|
|
FUT3
|
[NCBI]
|
2.55154e-05
|
|
|
SGKL
|
[NCBI]
|
2.47226e-05
|
|
|
KRT10
|
[NCBI]
|
2.47226e-05
|
|
|
HPS1
|
[NCBI]
|
2.40103e-05
|
|
|
breast cancer
|
[NCBI]
|
2.36392e-05
|
|
|
RP
|
[NCBI]
|
2.33077e-05
|
|
|
FOXE1
|
[NCBI]
|
2.27721e-05
|
|
|
CTNNA1
|
[NCBI]
|
2.27721e-05
|
|
|
ME2
|
[NCBI]
|
2.27721e-05
|
|
|
EFNB1
|
[NCBI]
|
2.27721e-05
|
|
|
PVRL1
|
[NCBI]
|
2.27721e-05
|
|
|
RCDP1
|
[NCBI]
|
2.21525e-05
|
|
|
WNT1
|
[NCBI]
|
2.17209e-05
|
|
|
HPS
|
[NCBI]
|
2.15007e-05
|
|
|
MYO5A
|
[NCBI]
|
2.08083e-05
|
|
|
RXRA
|
[NCBI]
|
2.08083e-05
|
|
|
CDSN
|
[NCBI]
|
2.03935e-05
|
|
|
PGM3
|
[NCBI]
|
2.03935e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
2.01329e-05
|
|
|
DSP
|
[NCBI]
|
2.00023e-05
|
|
|
LDHA
|
[NCBI]
|
1.96322e-05
|
|
|
POMC
|
[NCBI]
|
1.92818e-05
|
|
|
TRAF6
|
[NCBI]
|
1.9281e-05
|
|
|
SMN2
|
[NCBI]
|
1.86287e-05
|
|
|
COL17A1
|
[NCBI]
|
1.83246e-05
|
|
|
ATP7A
|
[NCBI]
|
1.80336e-05
|
|
|
TAF1
|
[NCBI]
|
1.80336e-05
|
|
|
BCHE
|
[NCBI]
|
1.79192e-05
|
|
|
CDKN1B
|
[NCBI]
|
1.74866e-05
|
|
|
DSG1
|
[NCBI]
|
1.72289e-05
|
|
|
EDNRB
|
[NCBI]
|
1.72289e-05
|
|
|
SCIDX1
|
[NCBI]
|
1.72283e-05
|
|
|
PGM1
|
[NCBI]
|
1.60712e-05
|
|
|
VDR
|
[NCBI]
|
1.57157e-05
|
|
|
SMA1
|
[NCBI]
|
1.57123e-05
|
|
|
CUTL1
|
[NCBI]
|
1.56593e-05
|
|
|
ACCN2
|
[NCBI]
|
1.54626e-05
|
|
|
danubian endemic familial nephropathy
|
[NCBI]
|
1.52394e-05
|
|
|
ACHE
|
[NCBI]
|
1.42947e-05
|
|
|
GFAP
|
[NCBI]
|
1.34124e-05
|
|
|
MTTL1
|
[NCBI]
|
1.31958e-05
|
|
|
homocystinuria
|
[NCBI]
|
1.29287e-05
|
|
|
metachromatic leukodystrophy
|
[NCBI]
|
1.26947e-05
|
|
|
COL2A1
|
[NCBI]
|
1.26725e-05
|
|
|
LNS
|
[NCBI]
|
1.23141e-05
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
1.16347e-05
|
|
|
KRT20
|
[NCBI]
|
1.15295e-05
|
|
|
CRH
|
[NCBI]
|
1.07407e-05
|
|
|
NPY
|
[NCBI]
|
1.06399e-05
|
|
|
wilson disease
|
[NCBI]
|
1.02498e-05
|
|
|
PTGS2
|
[NCBI]
|
9.58741e-06
|
|
|
ALD
|
[NCBI]
|
9.45726e-06
|
|
|
FGFR2
|
[NCBI]
|
8.6228e-06
|
|
|
BRCA1
|
[NCBI]
|
8.49769e-06
|
|
|
ABCC8
|
[NCBI]
|
8.25575e-06
|
|
|
CALCRL
|
[NCBI]
|
7.91203e-06
|
|
|
MITF
|
[NCBI]
|
7.80221e-06
|
|
|
BMP4
|
[NCBI]
|
7.5892e-06
|
|
|
G6PD
|
[NCBI]
|
7.49982e-06
|
|
|
RBP1
|
[NCBI]
|
7.33461e-06
|
|
|
MAP3K5
|
[NCBI]
|
6.99816e-06
|
|
|
DBI
|
[NCBI]
|
6.95187e-06
|
|
|
TS
|
[NCBI]
|
6.45955e-06
|
|
|
FGFR3
|
[NCBI]
|
5.9923e-06
|
|
|
HGF
|
[NCBI]
|
5.8126e-06
|
|
|
FMR1
|
[NCBI]
|
5.66394e-06
|
|
|
LDLR
|
[NCBI]
|
5.62887e-06
|
|
|
TP53
|
[NCBI]
|
5.49123e-06
|
|
|
EGF
|
[NCBI]
|
4.75703e-06
|
|
|
AS
|
[NCBI]
|
3.93811e-06
|
|
|
BDNF
|
[NCBI]
|
2.98897e-06
|
|
|
PTH
|
[NCBI]
|
2.87695e-06
|
|
|
SDC2
|
[NCBI]
|
2.6309e-06
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
2.53008e-06
|
|
|
LPL
|
[NCBI]
|
2.23852e-06
|
|
|
STAT3
|
[NCBI]
|
2.01955e-06
|
|
|
GJA1
|
[NCBI]
|
1.86428e-06
|
|
|
HD
|
[NCBI]
|
1.47497e-06
|
|
|
NGFB
|
[NCBI]
|
1.21327e-06
|
|
|
TNFSF6
|
[NCBI]
|
1.13179e-06
|
|
|
COMT
|
[NCBI]
|
1.04528e-06
|
|
|
PTK2
|
[NCBI]
|
6.9734e-07
|
|
|
PTHLH
|
[NCBI]
|
3.05955e-07
|
|
|
PWS
|
[NCBI]
|
1.9909e-07
|
|
|
ADA
|
[NCBI]
|
1.91125e-07
|
|
|
EGFR
|
[NCBI]
|
1.39233e-07
|
|
|
TH
|
[NCBI]
|
7.75618e-09
|
|
|
RNASE3
|
[NCBI]
|
3.65038e-09
|
|