|
OMIM |
Link |
Information gain |
01 |
|
peeling skin syndrome
|
[NCBI]
|
0.00297688
|
|
|
sneddon syndrome
|
[NCBI]
|
0.00297688
|
|
|
collagenosis, familial reactive perforating
|
[NCBI]
|
0.00264781
|
|
|
BZX
|
[NCBI]
|
0.00253238
|
|
|
malignant atrophic papulosis
|
[NCBI]
|
0.00244196
|
|
|
neutrophilic dermatosis, acute febrile
|
[NCBI]
|
0.0023163
|
|
|
comedones, familial dyskeratotic
|
[NCBI]
|
0.00192434
|
|
|
stiff skin syndrome
|
[NCBI]
|
0.001325
|
|
|
amyloidosis, primary cutaneous
|
[NCBI]
|
0.00125251
|
|
|
PDR
|
[NCBI]
|
0.00121674
|
|
|
LSA
|
[NCBI]
|
0.00112893
|
|
|
sebaceous gland hyperplasia, familial presenile
|
[NCBI]
|
0.0010823
|
|
|
dermochondrocorneal dystrophy
|
[NCBI]
|
0.000990409
|
|
|
tight skin contracture syndrome, lethal
|
[NCBI]
|
0.000970083
|
|
|
porphyria cutanea tarda
|
[NCBI]
|
0.000909476
|
|
|
EPS
|
[NCBI]
|
0.000788803
|
|
|
erythrokeratodermia with ataxia
|
[NCBI]
|
0.000756802
|
|
|
striae distensae, familial
|
[NCBI]
|
0.000756802
|
|
|
ameloonychohypohidrotic syndrome
|
[NCBI]
|
0.000756802
|
|
|
basaloid follicular hamartoma syndrome, generalized, autosomal dominant
|
[NCBI]
|
0.000756802
|
|
|
flynn-aird syndrome
|
[NCBI]
|
0.000756802
|
|
|
borrone dermatocardioskeletal syndrome
|
[NCBI]
|
0.000756802
|
|
|
EV
|
[NCBI]
|
0.000717046
|
|
|
DKC
|
[NCBI]
|
0.000639848
|
|
|
schimmelpenning-feuerstein-mims syndrome
|
[NCBI]
|
0.000628068
|
|
|
proteus syndrome
|
[NCBI]
|
0.000577283
|
|
|
nail dysplasia
|
[NCBI]
|
0.000540115
|
|
|
CMTC
|
[NCBI]
|
0.000539973
|
|
|
RA
|
[NCBI]
|
0.0005286
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.000461033
|
|
|
hyperimmunoglobulin e-recurrent infection syndrome, autosomal recessive
|
[NCBI]
|
0.000459121
|
|
|
mucoepithelial dysplasia, hereditary
|
[NCBI]
|
0.000459121
|
|
|
PN
|
[NCBI]
|
0.000459121
|
|
|
erythrokeratodermia variabilis 3
|
[NCBI]
|
0.000459121
|
|
|
pigmented purpuric eruption
|
[NCBI]
|
0.000459121
|
|
|
FDH
|
[NCBI]
|
0.000412633
|
|
|
onychotrichodysplasia and neutropenia
|
[NCBI]
|
0.00040697
|
|
|
acromial dimples
|
[NCBI]
|
0.00040697
|
|
|
focal facial dermal dysplasia
|
[NCBI]
|
0.00040697
|
|
|
telangiectasia, hereditary benign
|
[NCBI]
|
0.00040697
|
|
|
TRICY1
|
[NCBI]
|
0.00040697
|
|
|
cutis laxa, corneal clouding, and mental retardation
|
[NCBI]
|
0.000338133
|
|
|
PPPP
|
[NCBI]
|
0.000338133
|
|
|
SPG23
|
[NCBI]
|
0.00031308
|
|
|
AOS
|
[NCBI]
|
0.000308379
|
|
|
PXE
|
[NCBI]
|
0.000287122
|
|
|
porphyria cutanea tarda, type i
|
[NCBI]
|
0.000266739
|
|
|
dermatitis, atopic
|
[NCBI]
|
0.000257155
|
|
|
BHD
|
[NCBI]
|
0.000236307
|
|
|
porphyria variegata
|
[NCBI]
|
0.000229181
|
|
|
kindler syndrome
|
[NCBI]
|
0.000220814
|
|
|
RTS
|
[NCBI]
|
0.000211103
|
|
|
EKV
|
[NCBI]
|
0.000207424
|
|
|
facial ectodermal dysplasia
|
[NCBI]
|
0.000206969
|
|
|
ehlers-danlos syndrome, type vii, autosomal recessive
|
[NCBI]
|
0.000199102
|
|
|
ectodermal dysplasia/skin fragility syndrome
|
[NCBI]
|
0.000190762
|
|
|
CD
|
[NCBI]
|
0.000181569
|
|
|
KRT17
|
[NCBI]
|
0.000181255
|
|
|
IP
|
[NCBI]
|
0.000164745
|
|
|
MTS
|
[NCBI]
|
0.000146748
|
|
|
peeling skin syndrome, acral type
|
[NCBI]
|
0.000141048
|
|
|
pachyonychia congenita, recessive
|
[NCBI]
|
0.000141048
|
|
|
fountain syndrome
|
[NCBI]
|
0.000141048
|
|
|
NETH
|
[NCBI]
|
0.000127677
|
|
|
LOCS
|
[NCBI]
|
0.000127139
|
|
|
cardiomyopathy-hypogonadism-collagenoma syndrome
|
[NCBI]
|
0.000127139
|
|
|
MEN2A
|
[NCBI]
|
0.000124717
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.000117489
|
|
|
AIC
|
[NCBI]
|
0.000117489
|
|
|
DDD
|
[NCBI]
|
0.000117419
|
|
|
steatocystoma multiplex
|
[NCBI]
|
0.000110336
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
0.0001054
|
|
|
TGM5
|
[NCBI]
|
0.000100912
|
|
|
PKP1
|
[NCBI]
|
0.000100912
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.000100492
|
|
|
PC2
|
[NCBI]
|
9.52057e-05
|
|
|
dyskeratosis congenita, autosomal dominant
|
[NCBI]
|
9.14499e-05
|
|
|
DSAP1
|
[NCBI]
|
9.14499e-05
|
|
|
poland syndrome
|
[NCBI]
|
8.9573e-05
|
|
|
pseudoatrophoderma colli
|
[NCBI]
|
8.5943e-05
|
|
|
cutis verticis gyrata, thyroid aplasia, and mental retardation
|
[NCBI]
|
8.5943e-05
|
|
|
exostoses with anetodermia and brachydactyly, type e
|
[NCBI]
|
8.5943e-05
|
|
|
vasculitis, lymphocytic, nodular
|
[NCBI]
|
8.5943e-05
|
|
|
metaphyseal modeling abnormality, skin lesions, and spastic paraplegia
|
[NCBI]
|
8.5943e-05
|
|
|
macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance
|
[NCBI]
|
8.5943e-05
|
|
|
aplasia cutis congenita with intestinal lymphangiectasia
|
[NCBI]
|
8.5943e-05
|
|
|
arthropathy, erosive
|
[NCBI]
|
8.5943e-05
|
|
|
knuckle pads
|
[NCBI]
|
8.5943e-05
|
|
|
skin fragility-woolly hair syndrome
|
[NCBI]
|
8.5943e-05
|
|
|
WSS
|
[NCBI]
|
8.50832e-05
|
|
|
XPF
|
[NCBI]
|
8.50832e-05
|
|
|
HMI
|
[NCBI]
|
8.31498e-05
|
|
|
LOR
|
[NCBI]
|
8.11601e-05
|
|
|
congenital hemidysplasia with ichthyosiform erythroderma and limb defects
|
[NCBI]
|
7.98158e-05
|
|
|
PC1
|
[NCBI]
|
7.98158e-05
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
7.94691e-05
|
|
|
LDHA
|
[NCBI]
|
7.48507e-05
|
|
|
pseudoxanthoma elasticum, forme fruste
|
[NCBI]
|
7.33152e-05
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
7.13373e-05
|
|
|
buschke-ollendorff syndrome
|
[NCBI]
|
6.79796e-05
|
|
|
TTDP
|
[NCBI]
|
6.79796e-05
|
|
|
DSP
|
[NCBI]
|
6.74642e-05
|
|
|
bullous erythroderma ichthyosiformis congenita of brocq
|
[NCBI]
|
6.65521e-05
|
|
|
PDP
|
[NCBI]
|
6.63959e-05
|
|
|
CLCN4
|
[NCBI]
|
6.41994e-05
|
|
|
MPZL3
|
[NCBI]
|
6.41994e-05
|
|
|
KRT15
|
[NCBI]
|
6.41994e-05
|
|
|
PAI2
|
[NCBI]
|
6.41994e-05
|
|
|
PI3
|
[NCBI]
|
6.40903e-05
|
|
|
ABSD
|
[NCBI]
|
6.35512e-05
|
|
|
fascial dystrophy, congenital
|
[NCBI]
|
6.35512e-05
|
|
|
coxoauricular syndrome
|
[NCBI]
|
6.35512e-05
|
|
|
AMVC
|
[NCBI]
|
6.35512e-05
|
|
|
acroosteolysis
|
[NCBI]
|
6.35512e-05
|
|
|
poikiloderma, hereditary sclerosing
|
[NCBI]
|
6.35512e-05
|
|
|
skeletal dysplasia with telangiectases and mesodermal dysgenesis of the iris
|
[NCBI]
|
6.35512e-05
|
|
|
pellagra-like syndrome
|
[NCBI]
|
6.35512e-05
|
|
|
hyaluronan metabolism, defect in
|
[NCBI]
|
6.35512e-05
|
|
|
rombo syndrome
|
[NCBI]
|
6.35512e-05
|
|
|
tracheobronchomegaly
|
[NCBI]
|
6.35512e-05
|
|
|
MCOPCT3
|
[NCBI]
|
6.35512e-05
|
|
|
PEPD
|
[NCBI]
|
6.30851e-05
|
|
|
LMNA
|
[NCBI]
|
6.17595e-05
|
|
|
PLOD1
|
[NCBI]
|
6.12198e-05
|
|
|
lipoid proteinosis of urbach and wiethe
|
[NCBI]
|
6.08036e-05
|
|
|
GJB3
|
[NCBI]
|
6.03509e-05
|
|
|
MADA
|
[NCBI]
|
5.95601e-05
|
|
|
porphyria, congenital erythropoietic
|
[NCBI]
|
5.95601e-05
|
|
|
KRT14
|
[NCBI]
|
5.87232e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
5.83686e-05
|
|
|
steatocystoma multiplex with natal teeth
|
[NCBI]
|
5.515e-05
|
|
|
keratosis pilaris
|
[NCBI]
|
5.515e-05
|
|
|
NFTC
|
[NCBI]
|
5.515e-05
|
|
|
pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency
|
[NCBI]
|
5.515e-05
|
|
|
NS4
|
[NCBI]
|
5.515e-05
|
|
|
LDHCP
|
[NCBI]
|
5.515e-05
|
|
|
syringomas, multiple
|
[NCBI]
|
5.515e-05
|
|
|
muscular dystrophy, hemizygous lethal type
|
[NCBI]
|
5.515e-05
|
|
|
HFTC
|
[NCBI]
|
5.405e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
5.34861e-05
|
|
|
ABCC6
|
[NCBI]
|
5.33252e-05
|
|
|
MCOPS7
|
[NCBI]
|
5.21184e-05
|
|
|
EXOSC10
|
[NCBI]
|
5.04342e-05
|
|
|
KRT6B
|
[NCBI]
|
5.04342e-05
|
|
|
ichthyin
|
[NCBI]
|
5.04342e-05
|
|
|
ARHGAP6
|
[NCBI]
|
5.04342e-05
|
|
|
acrogeria, gottron type
|
[NCBI]
|
4.97225e-05
|
|
|
glomerulonephritis with sparse hair and telangiectases
|
[NCBI]
|
4.97225e-05
|
|
|
PKDTS
|
[NCBI]
|
4.97225e-05
|
|
|
dyskeratosis congenita, autosomal recessive
|
[NCBI]
|
4.97225e-05
|
|
|
majeed syndrome
|
[NCBI]
|
4.97225e-05
|
|
|
periodic fever, familial, autosomal dominant
|
[NCBI]
|
4.86215e-05
|
|
|
RCDP1
|
[NCBI]
|
4.86215e-05
|
|
|
OCA2
|
[NCBI]
|
4.70297e-05
|
|
|
GJB2
|
[NCBI]
|
4.685e-05
|
|
|
melanosis, neurocutaneous
|
[NCBI]
|
4.57075e-05
|
|
|
cutis gyrata syndrome of beare and stevenson
|
[NCBI]
|
4.57075e-05
|
|
|
angioma serpiginosum, autosomal dominant
|
[NCBI]
|
4.57075e-05
|
|
|
gastritis, familial giant hypertrophic
|
[NCBI]
|
4.57075e-05
|
|
|
knuckle pads, leukonychia, and sensorineural deafness
|
[NCBI]
|
4.57075e-05
|
|
|
cardiofaciocutaneous syndrome
|
[NCBI]
|
4.55278e-05
|
|
|
GTF2H5
|
[NCBI]
|
4.52483e-05
|
|
|
ITPKC
|
[NCBI]
|
4.52483e-05
|
|
|
ANTXR2
|
[NCBI]
|
4.52483e-05
|
|
|
TGFA
|
[NCBI]
|
4.52483e-05
|
|
|
SAMD9
|
[NCBI]
|
4.52483e-05
|
|
|
SDC4
|
[NCBI]
|
4.52483e-05
|
|
|
APOA1
|
[NCBI]
|
4.49476e-05
|
|
|
B2M
|
[NCBI]
|
4.31655e-05
|
|
|
BJS
|
[NCBI]
|
4.25243e-05
|
|
|
hyalinosis, infantile systemic
|
[NCBI]
|
4.25243e-05
|
|
|
vohwinkel syndrome, variant form
|
[NCBI]
|
4.25243e-05
|
|
|
pilomatrixoma
|
[NCBI]
|
4.25243e-05
|
|
|
cleft, median, of upper lip with polyps of facial skin and nasal mucosa
|
[NCBI]
|
4.25243e-05
|
|
|
TRAF1
|
[NCBI]
|
4.1886e-05
|
|
|
kindlin 1
|
[NCBI]
|
4.1886e-05
|
|
|
CCL17
|
[NCBI]
|
4.0932e-05
|
|
|
TS
|
[NCBI]
|
4.03722e-05
|
|
|
fabry disease
|
[NCBI]
|
4.02824e-05
|
|
|
ichthyosiform erythroderma, corneal involvement, and deafness
|
[NCBI]
|
3.98908e-05
|
|
|
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
|
[NCBI]
|
3.98908e-05
|
|
|
CINCA
|
[NCBI]
|
3.98908e-05
|
|
|
TTDN1
|
[NCBI]
|
3.98908e-05
|
|
|
ADCC
|
[NCBI]
|
3.98908e-05
|
|
|
NN
|
[NCBI]
|
3.98908e-05
|
|
|
GJB4
|
[NCBI]
|
3.93899e-05
|
|
|
TNFRSF8
|
[NCBI]
|
3.93899e-05
|
|
|
KLK5
|
[NCBI]
|
3.93899e-05
|
|
|
CST6
|
[NCBI]
|
3.93899e-05
|
|
|
SOS1
|
[NCBI]
|
3.93899e-05
|
|
|
LI1
|
[NCBI]
|
3.90995e-05
|
|
|
CSA
|
[NCBI]
|
3.79893e-05
|
|
|
VEGF
|
[NCBI]
|
3.77215e-05
|
|
|
melorheostosis
|
[NCBI]
|
3.76479e-05
|
|
|
TTDN1
|
[NCBI]
|
3.74038e-05
|
|
|
KLK3
|
[NCBI]
|
3.61863e-05
|
|
|
RXRA
|
[NCBI]
|
3.57548e-05
|
|
|
DCD
|
[NCBI]
|
3.57548e-05
|
|
|
KRT16
|
[NCBI]
|
3.57548e-05
|
|
|
IRF2
|
[NCBI]
|
3.57548e-05
|
|
|
ornithine transcarbamylase deficiency, hyperammonemia due to
|
[NCBI]
|
3.44596e-05
|
|
|
LPIN2
|
[NCBI]
|
3.43454e-05
|
|
|
ATP2C1
|
[NCBI]
|
3.43454e-05
|
|
|
ERCC4
|
[NCBI]
|
3.43454e-05
|
|
|
monilethrix
|
[NCBI]
|
3.39732e-05
|
|
|
PDCD4
|
[NCBI]
|
3.31152e-05
|
|
|
GALNT3
|
[NCBI]
|
3.31152e-05
|
|
|
megalencephaly-cutis marmorata telangiectatica congenita
|
[NCBI]
|
3.24303e-05
|
|
|
OSMED
|
[NCBI]
|
3.24303e-05
|
|
|
PTGS1
|
[NCBI]
|
3.10437e-05
|
|
|
GGCX
|
[NCBI]
|
3.10437e-05
|
|
|
MTC
|
[NCBI]
|
3.10355e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
3.10355e-05
|
|
|
severe cutaneous adverse reaction, susceptibility to
|
[NCBI]
|
3.10355e-05
|
|
|
PCNA
|
[NCBI]
|
3.02094e-05
|
|
|
NLRP3
|
[NCBI]
|
3.01543e-05
|
|
|
SGD
|
[NCBI]
|
2.97639e-05
|
|
|
SEDT
|
[NCBI]
|
2.97639e-05
|
|
|
deafness, congenital, with keratopachydermia and constrictions of fingers and toes
|
[NCBI]
|
2.97639e-05
|
|
|
IKBKB
|
[NCBI]
|
2.93406e-05
|
|
|
TCRB
|
[NCBI]
|
2.93406e-05
|
|
|
KLK7
|
[NCBI]
|
2.93406e-05
|
|
|
ALUNC
|
[NCBI]
|
2.85967e-05
|
|
|
PRKCM
|
[NCBI]
|
2.85907e-05
|
|
|
APC
|
[NCBI]
|
2.75267e-05
|
|
|
ichthyosis vulgaris
|
[NCBI]
|
2.75187e-05
|
|
|
HR
|
[NCBI]
|
2.7248e-05
|
|
|
KRT1
|
[NCBI]
|
2.66418e-05
|
|
|
kawasaki disease
|
[NCBI]
|
2.65181e-05
|
|
|
muckle-wells syndrome
|
[NCBI]
|
2.65181e-05
|
|
|
GVM
|
[NCBI]
|
2.65181e-05
|
|
|
severe combined immunodeficiency with sensitivity to ionizing radiation
|
[NCBI]
|
2.65181e-05
|
|
|
XPD
|
[NCBI]
|
2.65181e-05
|
|
|
tyrosine transaminase deficiency
|
[NCBI]
|
2.60723e-05
|
|
|
lymphoma, non-hodgkin, familial
|
[NCBI]
|
2.56956e-05
|
|
|
CGD
|
[NCBI]
|
2.56442e-05
|
|
|
EPPK
|
[NCBI]
|
2.55852e-05
|
|
|
synovitis, granulomatous, with uveitis and cranial neuropathies
|
[NCBI]
|
2.55852e-05
|
|
|
C4B
|
[NCBI]
|
2.55353e-05
|
|
|
ECM1
|
[NCBI]
|
2.55353e-05
|
|
|
GJB6
|
[NCBI]
|
2.50274e-05
|
|
|
DKC1
|
[NCBI]
|
2.50274e-05
|
|
|
CYLD
|
[NCBI]
|
2.47119e-05
|
|
|
amyloidosis v
|
[NCBI]
|
2.47119e-05
|
|
|
erythermalgia, primary
|
[NCBI]
|
2.47119e-05
|
|
|
ED2
|
[NCBI]
|
2.47119e-05
|
|
|
keratitis-ichthyosis-deafness syndrome, autosomal dominant
|
[NCBI]
|
2.47119e-05
|
|
|
TNFSF8
|
[NCBI]
|
2.45458e-05
|
|
|
HLA-B
|
[NCBI]
|
2.45458e-05
|
|
|
CDPX1
|
[NCBI]
|
2.38918e-05
|
|
|
holocarboxylase synthetase deficiency
|
[NCBI]
|
2.38918e-05
|
|
|
hartnup disorder
|
[NCBI]
|
2.31191e-05
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
2.23892e-05
|
|
|
AGS1
|
[NCBI]
|
2.23892e-05
|
|
|
ERCC2
|
[NCBI]
|
2.20868e-05
|
|
|
XPC
|
[NCBI]
|
2.20868e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
2.16979e-05
|
|
|
KLF4
|
[NCBI]
|
2.10672e-05
|
|
|
AFD1
|
[NCBI]
|
2.10417e-05
|
|
|
MNS
|
[NCBI]
|
2.10417e-05
|
|
|
TRPS1
|
[NCBI]
|
2.10417e-05
|
|
|
AHO
|
[NCBI]
|
2.09093e-05
|
|
|
aspartylglucosaminuria
|
[NCBI]
|
2.07514e-05
|
|
|
HIDS
|
[NCBI]
|
2.04176e-05
|
|
|
APL
|
[NCBI]
|
2.04176e-05
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
1.98228e-05
|
|
|
C3
|
[NCBI]
|
1.95885e-05
|
|
|
GLA
|
[NCBI]
|
1.932e-05
|
|
|
ALK
|
[NCBI]
|
1.91166e-05
|
|
|
DSG1
|
[NCBI]
|
1.90594e-05
|
|
|
LOX
|
[NCBI]
|
1.90594e-05
|
|
|
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant
|
[NCBI]
|
1.87124e-05
|
|
|
CD
|
[NCBI]
|
1.86952e-05
|
|
|
PTH
|
[NCBI]
|
1.86609e-05
|
|
|
OA1
|
[NCBI]
|
1.85602e-05
|
|
|
FGF7
|
[NCBI]
|
1.82816e-05
|
|
|
OFD1
|
[NCBI]
|
1.81928e-05
|
|
|
biotinidase deficiency
|
[NCBI]
|
1.81928e-05
|
|
|
FGFR3
|
[NCBI]
|
1.79183e-05
|
|
|
RBP1
|
[NCBI]
|
1.7861e-05
|
|
|
epidermolysis bullosa letalis
|
[NCBI]
|
1.76947e-05
|
|
|
EBR1
|
[NCBI]
|
1.72165e-05
|
|
|
COL7A1
|
[NCBI]
|
1.72138e-05
|
|
|
RNASE3
|
[NCBI]
|
1.71458e-05
|
|
|
MC1R
|
[NCBI]
|
1.70085e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
1.6757e-05
|
|
|
TPMT
|
[NCBI]
|
1.6612e-05
|
|
|
LCN2
|
[NCBI]
|
1.64204e-05
|
|
|
FMF
|
[NCBI]
|
1.62639e-05
|
|
|
FGF23
|
[NCBI]
|
1.62331e-05
|
|
|
MSH2
|
[NCBI]
|
1.60498e-05
|
|
|
OCRL
|
[NCBI]
|
1.54787e-05
|
|
|
FPLD2
|
[NCBI]
|
1.54787e-05
|
|
|
FCAS
|
[NCBI]
|
1.47005e-05
|
|
|
UCN
|
[NCBI]
|
1.45596e-05
|
|
|
CDPX2
|
[NCBI]
|
1.43311e-05
|
|
|
apert syndrome
|
[NCBI]
|
1.43311e-05
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
1.39738e-05
|
|
|
protein c deficiency, congenital thrombotic disease due to
|
[NCBI]
|
1.38353e-05
|
|
|
ehlers-danlos syndrome, type iv, autosomal dominant
|
[NCBI]
|
1.36281e-05
|
|
|
CNC1
|
[NCBI]
|
1.32934e-05
|
|
|
MPO
|
[NCBI]
|
1.29273e-05
|
|
|
MLH1
|
[NCBI]
|
1.27975e-05
|
|
|
POMC
|
[NCBI]
|
1.24221e-05
|
|
|
XPA
|
[NCBI]
|
1.17658e-05
|
|
|
BCPM
|
[NCBI]
|
1.1215e-05
|
|
|
CTGF
|
[NCBI]
|
1.11681e-05
|
|
|
MPZ
|
[NCBI]
|
1.10643e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
9.73321e-06
|
|
|
costello syndrome
|
[NCBI]
|
9.50827e-06
|
|
|
CEACAM5
|
[NCBI]
|
9.0302e-06
|
|
|
sickle cell anemia
|
[NCBI]
|
8.86664e-06
|
|
|
RET
|
[NCBI]
|
8.23206e-06
|
|
|
HMBS
|
[NCBI]
|
8.23206e-06
|
|
|
porphyria, acute intermittent
|
[NCBI]
|
8.08155e-06
|
|
|
AR
|
[NCBI]
|
7.86811e-06
|
|
|
temporal arteritis
|
[NCBI]
|
7.81692e-06
|
|
|
PTEN
|
[NCBI]
|
7.61979e-06
|
|
|
FGFR2
|
[NCBI]
|
7.61979e-06
|
|
|
APRT
|
[NCBI]
|
7.56173e-06
|
|
|
CRMO
|
[NCBI]
|
7.3675e-06
|
|
|
SDC2
|
[NCBI]
|
6.80238e-06
|
|
|
apc gene
|
[NCBI]
|
6.75168e-06
|
|
|
ALGS1
|
[NCBI]
|
6.56194e-06
|
|
|
CVID
|
[NCBI]
|
6.48059e-06
|
|
|
OCP
|
[NCBI]
|
5.84053e-06
|
|
|
MBP
|
[NCBI]
|
5.76125e-06
|
|
|
HGPS
|
[NCBI]
|
5.70534e-06
|
|
|
BLM
|
[NCBI]
|
5.70534e-06
|
|
|
NPY
|
[NCBI]
|
5.56387e-06
|
|
|
FOP
|
[NCBI]
|
5.44343e-06
|
|
|
CRH
|
[NCBI]
|
5.39246e-06
|
|
|
HGF
|
[NCBI]
|
5.25745e-06
|
|
|
PSORS1
|
[NCBI]
|
4.95148e-06
|
|
|
TTR
|
[NCBI]
|
4.82379e-06
|
|
|
DFSP
|
[NCBI]
|
3.93647e-06
|
|
|
EGF
|
[NCBI]
|
3.62522e-06
|
|
|
ACHE
|
[NCBI]
|
3.1867e-06
|
|
|
TH
|
[NCBI]
|
3.13898e-06
|
|
|
hypercholesterolemia, autosomal dominant
|
[NCBI]
|
3.01347e-06
|
|
|
EGFR
|
[NCBI]
|
2.57839e-06
|
|
|
AT
|
[NCBI]
|
2.41373e-06
|
|
|
MUC1
|
[NCBI]
|
2.39213e-06
|
|
|
IL2
|
[NCBI]
|
2.35904e-06
|
|
|
HP
|
[NCBI]
|
1.99726e-06
|
|
|
MAS
|
[NCBI]
|
1.77076e-06
|
|
|
GAPDH
|
[NCBI]
|
1.76659e-06
|
|
|
ADA
|
[NCBI]
|
1.75466e-06
|
|
|
WAS
|
[NCBI]
|
1.69128e-06
|
|
|
PF4
|
[NCBI]
|
1.4526e-06
|
|
|
VHL
|
[NCBI]
|
1.37681e-06
|
|
|
G6PD
|
[NCBI]
|
1.19461e-06
|
|
|
VIP
|
[NCBI]
|
7.81442e-07
|
|
|
TNF
|
[NCBI]
|
7.42068e-07
|
|
|
KSS
|
[NCBI]
|
5.45482e-07
|
|
|
HPS
|
[NCBI]
|
5.20563e-07
|
|
|
PTK2
|
[NCBI]
|
4.44925e-07
|
|
|
TYMS
|
[NCBI]
|
3.4985e-07
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.17939e-07
|
|
|
BCNS
|
[NCBI]
|
1.95583e-07
|
|
|
CAT
|
[NCBI]
|
1.02038e-07
|
|
|
SLOS
|
[NCBI]
|
8.04133e-08
|
|
|
APOB
|
[NCBI]
|
6.83012e-08
|
|
|
LAM
|
[NCBI]
|
3.8456e-08
|
|
|
SLE
|
[NCBI]
|
2.66443e-08
|
|
|
APOE
|
[NCBI]
|
7.35177e-09
|
|
|
SPP1
|
[NCBI]
|
5.85502e-09
|
|
|
CHAT
|
[NCBI]
|
2.55016e-10
|
|