|
OMIM |
Link |
Information gain |
01 |
|
urogenital adysplasia, hereditary
|
[NCBI]
|
0.00227211
|
|
|
ACC
|
[NCBI]
|
0.00156493
|
|
|
fingerprints, absence of
|
[NCBI]
|
0.00149916
|
|
|
oculodentoosseous dysplasia, recessive
|
[NCBI]
|
0.00106589
|
|
|
SHFM1
|
[NCBI]
|
0.00103998
|
|
|
pyloric atresia
|
[NCBI]
|
0.000974062
|
|
|
BDA3
|
[NCBI]
|
0.000748579
|
|
|
pseudomonilethrix
|
[NCBI]
|
0.000748579
|
|
|
ureter, bifid or double
|
[NCBI]
|
0.000748579
|
|
|
polydactyly, preaxial iii
|
[NCBI]
|
0.000748579
|
|
|
RA
|
[NCBI]
|
0.000647291
|
|
|
AFP
|
[NCBI]
|
0.000626107
|
|
|
DWS
|
[NCBI]
|
0.000614178
|
|
|
PTLAH
|
[NCBI]
|
0.000531961
|
|
|
ocular hypotelorism, submucosal cleft palate, and hypospadias
|
[NCBI]
|
0.000531961
|
|
|
teeth, odd shapes of
|
[NCBI]
|
0.000531961
|
|
|
TARPS
|
[NCBI]
|
0.000531961
|
|
|
polysyndactyly, crossed
|
[NCBI]
|
0.000531961
|
|
|
aural atresia, congenital
|
[NCBI]
|
0.000531961
|
|
|
brachydactyly, combined b and e types
|
[NCBI]
|
0.000531961
|
|
|
clubbing of digits
|
[NCBI]
|
0.000531961
|
|
|
MCOPCT1
|
[NCBI]
|
0.000531961
|
|
|
basilar impression, primary
|
[NCBI]
|
0.000451036
|
|
|
laterality defects, autosomal dominant
|
[NCBI]
|
0.000451036
|
|
|
OFD8
|
[NCBI]
|
0.000451036
|
|
|
van der woude syndrome modifier
|
[NCBI]
|
0.000451036
|
|
|
megalencephaly
|
[NCBI]
|
0.000451036
|
|
|
triphalangeal thumbs with brachyectrodactyly
|
[NCBI]
|
0.000451036
|
|
|
dermal ridges, patternless
|
[NCBI]
|
0.000451036
|
|
|
renal-hepatic-pancreatic dysplasia with dandy-walker cyst
|
[NCBI]
|
0.000398954
|
|
|
camptodactyly
|
[NCBI]
|
0.000398954
|
|
|
SLE
|
[NCBI]
|
0.000374006
|
|
|
molar i reinclusion
|
[NCBI]
|
0.000360571
|
|
|
cerebral palsy, ataxic, autosomal recessive
|
[NCBI]
|
0.000360571
|
|
|
holoprosencephaly
|
[NCBI]
|
0.00034572
|
|
|
OFD9
|
[NCBI]
|
0.000330256
|
|
|
maxillonasal dysplasia, binder type
|
[NCBI]
|
0.000330256
|
|
|
trichomegaly with mental retardation, dwarfism, and pigmentary degeneration of retina
|
[NCBI]
|
0.000330256
|
|
|
leukonychia totalis
|
[NCBI]
|
0.000330256
|
|
|
MDLS
|
[NCBI]
|
0.000306805
|
|
|
microtia with meatal atresia and conductive deafness
|
[NCBI]
|
0.000265717
|
|
|
acetabular dysplasia
|
[NCBI]
|
0.000265717
|
|
|
aniridia, cerebellar ataxia, and mental deficiency
|
[NCBI]
|
0.000265717
|
|
|
hypertension with brachydactyly
|
[NCBI]
|
0.000265717
|
|
|
acrodysostosis
|
[NCBI]
|
0.000265717
|
|
|
THAS
|
[NCBI]
|
0.000249555
|
|
|
PCA
|
[NCBI]
|
0.000249555
|
|
|
MCOPS1
|
[NCBI]
|
0.00023515
|
|
|
IH
|
[NCBI]
|
0.000222181
|
|
|
ZLS
|
[NCBI]
|
0.000222181
|
|
|
CBAVD
|
[NCBI]
|
0.000213689
|
|
|
OSCS
|
[NCBI]
|
0.000199645
|
|
|
AMCN
|
[NCBI]
|
0.000199645
|
|
|
AN1
|
[NCBI]
|
0.000198333
|
|
|
polydactyly, postaxial, type a1
|
[NCBI]
|
0.000198333
|
|
|
OFD1
|
[NCBI]
|
0.000193623
|
|
|
pulmonary hypoplasia, primary
|
[NCBI]
|
0.000189199
|
|
|
gallbladder, agenesis of
|
[NCBI]
|
0.000189199
|
|
|
TCOF
|
[NCBI]
|
0.00018806
|
|
|
PAFAH1B1
|
[NCBI]
|
0.000173229
|
|
|
SHFM3
|
[NCBI]
|
0.000164207
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.000164207
|
|
|
blepharochalasis and double lip
|
[NCBI]
|
0.000158292
|
|
|
uterine anomalies
|
[NCBI]
|
0.000158292
|
|
|
macrocephaly
|
[NCBI]
|
0.000158292
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
0.000153129
|
|
|
asplenia with cardiovascular anomalies
|
[NCBI]
|
0.000147645
|
|
|
ACHE
|
[NCBI]
|
0.000140474
|
|
|
MESDC2
|
[NCBI]
|
0.000137217
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
0.000137216
|
|
|
PPS
|
[NCBI]
|
0.000136226
|
|
|
CVG/MR
|
[NCBI]
|
0.000134791
|
|
|
HFM
|
[NCBI]
|
0.000132513
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.00012592
|
|
|
diaphragmatic hernia, congenital
|
[NCBI]
|
0.00012592
|
|
|
polydactyly, preaxial i
|
[NCBI]
|
0.000121547
|
|
|
pancreas, annular
|
[NCBI]
|
0.000121547
|
|
|
SHH
|
[NCBI]
|
0.000117671
|
|
|
gastroschisis
|
[NCBI]
|
0.000116557
|
|
|
NLS
|
[NCBI]
|
0.000115768
|
|
|
phenylketonuria
|
[NCBI]
|
0.000107349
|
|
|
CPI
|
[NCBI]
|
0.000102476
|
|
|
wagr syndrome
|
[NCBI]
|
0.000102025
|
|
|
BWS
|
[NCBI]
|
0.000101174
|
|
|
ED1
|
[NCBI]
|
9.84743e-05
|
|
|
SLOS
|
[NCBI]
|
9.63498e-05
|
|
|
charcot-marie-tooth peroneal muscular atrophy and friedreich ataxia, combined
|
[NCBI]
|
9.45686e-05
|
|
|
mesomelic dysplasia, savarirayan type
|
[NCBI]
|
9.45686e-05
|
|
|
ear folding
|
[NCBI]
|
9.45686e-05
|
|
|
coracoclavicular joint, anomalous
|
[NCBI]
|
9.45686e-05
|
|
|
adactylia, unilateral
|
[NCBI]
|
9.45686e-05
|
|
|
leukomelanoderma, infantilism, mental retardation, hypodontia, hypotrichosis
|
[NCBI]
|
9.45686e-05
|
|
|
bowen syndrome of multiple malformations
|
[NCBI]
|
9.45686e-05
|
|
|
vertebral fusion, posterior lumbosacral, with blepharoptosis
|
[NCBI]
|
9.45686e-05
|
|
|
syndactyly with renal and anogenital malformations
|
[NCBI]
|
9.45686e-05
|
|
|
thoracic dysostosis, isolated
|
[NCBI]
|
9.45686e-05
|
|
|
retinal venous beading
|
[NCBI]
|
9.45686e-05
|
|
|
cryptotia, familial
|
[NCBI]
|
9.45686e-05
|
|
|
thumbs, congenital clasped
|
[NCBI]
|
9.45686e-05
|
|
|
skin fragility-woolly hair syndrome
|
[NCBI]
|
9.45686e-05
|
|
|
fraser-like syndrome
|
[NCBI]
|
9.45686e-05
|
|
|
woolly hair, hypotrichosis, everted lower lip, and outstanding ears
|
[NCBI]
|
9.45686e-05
|
|
|
mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones
|
[NCBI]
|
9.45686e-05
|
|
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
9.43461e-05
|
|
|
PFM
|
[NCBI]
|
9.43313e-05
|
|
|
HOXA1
|
[NCBI]
|
9.25567e-05
|
|
|
MBS
|
[NCBI]
|
8.70532e-05
|
|
|
JLNS1
|
[NCBI]
|
8.46541e-05
|
|
|
crouzon syndrome
|
[NCBI]
|
8.46541e-05
|
|
|
RTD
|
[NCBI]
|
8.30369e-05
|
|
|
CF
|
[NCBI]
|
8.23313e-05
|
|
|
EEC1
|
[NCBI]
|
8.03575e-05
|
|
|
CACNA1S
|
[NCBI]
|
7.87944e-05
|
|
|
ATD1
|
[NCBI]
|
7.72122e-05
|
|
|
MADA
|
[NCBI]
|
7.60337e-05
|
|
|
donohue syndrome
|
[NCBI]
|
7.48087e-05
|
|
|
laryngeal abductor paralysis
|
[NCBI]
|
7.21434e-05
|
|
|
lymphedema and ptosis
|
[NCBI]
|
7.21434e-05
|
|
|
DHS
|
[NCBI]
|
7.21434e-05
|
|
|
anus, imperforate
|
[NCBI]
|
7.21434e-05
|
|
|
tracheobronchomegaly
|
[NCBI]
|
7.21434e-05
|
|
|
arthrogryposis-like hand anomaly and sensorineural deafness
|
[NCBI]
|
7.21434e-05
|
|
|
MCOPCT3
|
[NCBI]
|
7.21434e-05
|
|
|
hypothalamic hamartomas
|
[NCBI]
|
7.21434e-05
|
|
|
ectrodactyly of lower limbs, congenital heart defect, and micrognathia
|
[NCBI]
|
7.21434e-05
|
|
|
WT1
|
[NCBI]
|
7.09385e-05
|
|
|
CHNG2
|
[NCBI]
|
7.03563e-05
|
|
|
TBRG4
|
[NCBI]
|
6.85746e-05
|
|
|
CCT7
|
[NCBI]
|
6.85746e-05
|
|
|
DNAJA2
|
[NCBI]
|
6.85746e-05
|
|
|
CCPG1
|
[NCBI]
|
6.85746e-05
|
|
|
ORC3L
|
[NCBI]
|
6.85746e-05
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
6.58158e-05
|
|
|
ODDD
|
[NCBI]
|
6.55933e-05
|
|
|
cerebellar ataxia and ectodermal dysplasia
|
[NCBI]
|
6.37086e-05
|
|
|
male infertility with large-headed, multiflagellar, polyploid spermatozoa
|
[NCBI]
|
6.37086e-05
|
|
|
craniotelencephalic dysplasia
|
[NCBI]
|
6.37086e-05
|
|
|
corpus callosum, partial agenesis of, x-linked
|
[NCBI]
|
6.37086e-05
|
|
|
ear pits, posterior helical
|
[NCBI]
|
6.37086e-05
|
|
|
autism
|
[NCBI]
|
6.3233e-05
|
|
|
CDLS1
|
[NCBI]
|
6.30927e-05
|
|
|
hypogonadism, male
|
[NCBI]
|
5.82477e-05
|
|
|
varicose veins
|
[NCBI]
|
5.82477e-05
|
|
|
HPE5
|
[NCBI]
|
5.82477e-05
|
|
|
anal atresia, hypospadias, and penoscrotal inversion
|
[NCBI]
|
5.82477e-05
|
|
|
ectopia lentis
|
[NCBI]
|
5.82477e-05
|
|
|
pachygyria with mental retardation and seizures
|
[NCBI]
|
5.82477e-05
|
|
|
pierre robin syndrome
|
[NCBI]
|
5.82477e-05
|
|
|
axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
|
[NCBI]
|
5.82477e-05
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
5.60427e-05
|
|
|
CSDE1
|
[NCBI]
|
5.48038e-05
|
|
|
UNC5C
|
[NCBI]
|
5.48038e-05
|
|
|
CRK
|
[NCBI]
|
5.48038e-05
|
|
|
twirler mutation, murine, human homolog of
|
[NCBI]
|
5.48038e-05
|
|
|
CASP6
|
[NCBI]
|
5.48038e-05
|
|
|
polydactyly
|
[NCBI]
|
5.41992e-05
|
|
|
polydactyly, preaxial iv
|
[NCBI]
|
5.41992e-05
|
|
|
larynx, congenital partial atresia of
|
[NCBI]
|
5.41992e-05
|
|
|
LISX2
|
[NCBI]
|
5.41992e-05
|
|
|
splenogonadal fusion with limb defects and micrognathia
|
[NCBI]
|
5.41992e-05
|
|
|
SRS
|
[NCBI]
|
5.10413e-05
|
|
|
chromosome 18p deletion syndrome
|
[NCBI]
|
5.09825e-05
|
|
|
cleft larynx, posterior
|
[NCBI]
|
5.09825e-05
|
|
|
bowing of legs, anterior, with dwarfism
|
[NCBI]
|
5.09825e-05
|
|
|
syndactyly, type iii
|
[NCBI]
|
5.09825e-05
|
|
|
duodenal atresia
|
[NCBI]
|
5.09825e-05
|
|
|
MKS1
|
[NCBI]
|
4.97949e-05
|
|
|
CASP7
|
[NCBI]
|
4.96124e-05
|
|
|
WS1
|
[NCBI]
|
4.92972e-05
|
|
|
VEGF
|
[NCBI]
|
4.85762e-05
|
|
|
EHBA
|
[NCBI]
|
4.83156e-05
|
|
|
epidermolysis bullosa with congenital localized absence of skin and deformity of nails
|
[NCBI]
|
4.83156e-05
|
|
|
ADCC
|
[NCBI]
|
4.83156e-05
|
|
|
anonychia congenita
|
[NCBI]
|
4.83156e-05
|
|
|
FGA
|
[NCBI]
|
4.8178e-05
|
|
|
ATOX1
|
[NCBI]
|
4.62445e-05
|
|
|
WARBM
|
[NCBI]
|
4.60392e-05
|
|
|
cataract-microcornea syndrome
|
[NCBI]
|
4.60392e-05
|
|
|
ALSG
|
[NCBI]
|
4.60392e-05
|
|
|
ectopia lentis, isolated
|
[NCBI]
|
4.60392e-05
|
|
|
HMS
|
[NCBI]
|
4.60392e-05
|
|
|
oeis complex
|
[NCBI]
|
4.60392e-05
|
|
|
situs inversus viscerum
|
[NCBI]
|
4.60392e-05
|
|
|
NPS
|
[NCBI]
|
4.56172e-05
|
|
|
LIS1
|
[NCBI]
|
4.4055e-05
|
|
|
corpus callosum, agenesis of
|
[NCBI]
|
4.4055e-05
|
|
|
metaphyseal chondrodysplasia, jansen type
|
[NCBI]
|
4.4055e-05
|
|
|
globozoospermia
|
[NCBI]
|
4.4055e-05
|
|
|
cerebral palsy, spastic, symmetric, autosomal recessive
|
[NCBI]
|
4.4055e-05
|
|
|
whistling face syndrome, recessive form
|
[NCBI]
|
4.4055e-05
|
|
|
EN1
|
[NCBI]
|
4.37428e-05
|
|
|
NCOA6
|
[NCBI]
|
4.37428e-05
|
|
|
CASP2
|
[NCBI]
|
4.37428e-05
|
|
|
YWHAE
|
[NCBI]
|
4.37428e-05
|
|
|
chondrodysplasia, grebe type
|
[NCBI]
|
4.22976e-05
|
|
|
pierson syndrome
|
[NCBI]
|
4.22976e-05
|
|
|
BOCD
|
[NCBI]
|
4.22976e-05
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
4.22976e-05
|
|
|
ASMD
|
[NCBI]
|
4.22976e-05
|
|
|
LISX1
|
[NCBI]
|
4.22976e-05
|
|
|
monilethrix
|
[NCBI]
|
4.22976e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
4.22976e-05
|
|
|
BDA1
|
[NCBI]
|
4.22976e-05
|
|
|
EMX2
|
[NCBI]
|
4.17512e-05
|
|
|
CHD7
|
[NCBI]
|
4.17512e-05
|
|
|
PGP
|
[NCBI]
|
4.17512e-05
|
|
|
CHX10
|
[NCBI]
|
4.17512e-05
|
|
|
AHR
|
[NCBI]
|
4.14963e-05
|
|
|
TNF
|
[NCBI]
|
4.09272e-05
|
|
|
omphalocele
|
[NCBI]
|
4.07212e-05
|
|
|
PDV
|
[NCBI]
|
4.07212e-05
|
|
|
gracile syndrome
|
[NCBI]
|
4.07212e-05
|
|
|
pseudotrisomy 13 syndrome
|
[NCBI]
|
4.07212e-05
|
|
|
LAMB2
|
[NCBI]
|
4.00967e-05
|
|
|
CYP11A1
|
[NCBI]
|
4.00967e-05
|
|
|
wildervanck syndrome
|
[NCBI]
|
3.92929e-05
|
|
|
chromosome 18q deletion syndrome
|
[NCBI]
|
3.92929e-05
|
|
|
IRID2
|
[NCBI]
|
3.92929e-05
|
|
|
THBS1
|
[NCBI]
|
3.86817e-05
|
|
|
IGF2R
|
[NCBI]
|
3.86817e-05
|
|
|
BMP15
|
[NCBI]
|
3.86817e-05
|
|
|
UBB
|
[NCBI]
|
3.86817e-05
|
|
|
ACCPN
|
[NCBI]
|
3.79879e-05
|
|
|
cystathioninuria
|
[NCBI]
|
3.79879e-05
|
|
|
hyperprolinemia, type i
|
[NCBI]
|
3.79879e-05
|
|
|
FOLR1
|
[NCBI]
|
3.74459e-05
|
|
|
CASP3
|
[NCBI]
|
3.74459e-05
|
|
|
EFNB1
|
[NCBI]
|
3.74459e-05
|
|
|
CEBPA
|
[NCBI]
|
3.74459e-05
|
|
|
POMGNT1
|
[NCBI]
|
3.74459e-05
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
3.67872e-05
|
|
|
HPE2
|
[NCBI]
|
3.67872e-05
|
|
|
hemochromatosis, neonatal
|
[NCBI]
|
3.67872e-05
|
|
|
ACG2
|
[NCBI]
|
3.67872e-05
|
|
|
PXMP3
|
[NCBI]
|
3.63491e-05
|
|
|
LMBR1
|
[NCBI]
|
3.63491e-05
|
|
|
BDC
|
[NCBI]
|
3.56757e-05
|
|
|
fibromuscular dysplasia of arteries
|
[NCBI]
|
3.56757e-05
|
|
|
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1
|
[NCBI]
|
3.56757e-05
|
|
|
pituitary dwarfism i
|
[NCBI]
|
3.56757e-05
|
|
|
HOXA13
|
[NCBI]
|
3.53633e-05
|
|
|
PITX3
|
[NCBI]
|
3.53633e-05
|
|
|
FA
|
[NCBI]
|
3.46923e-05
|
|
|
SPD1
|
[NCBI]
|
3.46416e-05
|
|
|
pitt syndrome
|
[NCBI]
|
3.46416e-05
|
|
|
CHNG1
|
[NCBI]
|
3.46416e-05
|
|
|
BOS1
|
[NCBI]
|
3.46416e-05
|
|
|
DGI1
|
[NCBI]
|
3.46416e-05
|
|
|
DCX
|
[NCBI]
|
3.44684e-05
|
|
|
SALL1
|
[NCBI]
|
3.44684e-05
|
|
|
HBZ
|
[NCBI]
|
3.3649e-05
|
|
|
SURF1
|
[NCBI]
|
3.28936e-05
|
|
|
NETH
|
[NCBI]
|
3.27686e-05
|
|
|
papillorenal syndrome
|
[NCBI]
|
3.27686e-05
|
|
|
EDM1
|
[NCBI]
|
3.27686e-05
|
|
|
pycnodysostosis
|
[NCBI]
|
3.27686e-05
|
|
|
abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism
|
[NCBI]
|
3.19149e-05
|
|
|
HOXD13
|
[NCBI]
|
3.15398e-05
|
|
|
farber lipogranulomatosis
|
[NCBI]
|
3.15398e-05
|
|
|
NHS
|
[NCBI]
|
3.11088e-05
|
|
|
CIPA
|
[NCBI]
|
3.11088e-05
|
|
|
diarrhea 1, secretory chloride, congenital
|
[NCBI]
|
3.11088e-05
|
|
|
SLC2A1
|
[NCBI]
|
3.09281e-05
|
|
|
DSP
|
[NCBI]
|
3.09281e-05
|
|
|
MSX1
|
[NCBI]
|
3.09281e-05
|
|
|
TBX1
|
[NCBI]
|
3.09281e-05
|
|
|
CMDD
|
[NCBI]
|
3.03454e-05
|
|
|
ZS
|
[NCBI]
|
2.9885e-05
|
|
|
GJA8
|
[NCBI]
|
2.98105e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
2.96206e-05
|
|
|
periodontitis, aggressive, 1
|
[NCBI]
|
2.96206e-05
|
|
|
AFD1
|
[NCBI]
|
2.89309e-05
|
|
|
HSAN1
|
[NCBI]
|
2.89309e-05
|
|
|
TCOF1
|
[NCBI]
|
2.83463e-05
|
|
|
CPX
|
[NCBI]
|
2.82733e-05
|
|
|
HSS
|
[NCBI]
|
2.82733e-05
|
|
|
transcobalamin ii deficiency
|
[NCBI]
|
2.79043e-05
|
|
|
NR5A1
|
[NCBI]
|
2.66899e-05
|
|
|
neural tube defects
|
[NCBI]
|
2.64678e-05
|
|
|
SOX9
|
[NCBI]
|
2.59592e-05
|
|
|
hyperglycerolemia
|
[NCBI]
|
2.59147e-05
|
|
|
GPC3
|
[NCBI]
|
2.49599e-05
|
|
|
OKS
|
[NCBI]
|
2.48714e-05
|
|
|
BMP4
|
[NCBI]
|
2.46492e-05
|
|
|
MKKS
|
[NCBI]
|
2.43784e-05
|
|
|
leopard syndrome 1
|
[NCBI]
|
2.43784e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
2.43784e-05
|
|
|
NR0B1
|
[NCBI]
|
2.40572e-05
|
|
|
GDXY
|
[NCBI]
|
2.40572e-05
|
|
|
SCDO1
|
[NCBI]
|
2.34436e-05
|
|
|
EFE
|
[NCBI]
|
2.34436e-05
|
|
|
OCRL
|
[NCBI]
|
2.29998e-05
|
|
|
SGBS1
|
[NCBI]
|
2.29998e-05
|
|
|
RS1
|
[NCBI]
|
2.27243e-05
|
|
|
LHCGR
|
[NCBI]
|
2.27243e-05
|
|
|
DA2A
|
[NCBI]
|
2.25704e-05
|
|
|
EVA
|
[NCBI]
|
2.21546e-05
|
|
|
TBS
|
[NCBI]
|
2.17517e-05
|
|
|
RCDP1
|
[NCBI]
|
2.17517e-05
|
|
|
SEDC
|
[NCBI]
|
2.17517e-05
|
|
|
charge syndrome
|
[NCBI]
|
2.13609e-05
|
|
|
MEB
|
[NCBI]
|
2.13609e-05
|
|
|
HMI
|
[NCBI]
|
2.11336e-05
|
|
|
EVC
|
[NCBI]
|
2.09817e-05
|
|
|
OCA2
|
[NCBI]
|
2.09817e-05
|
|
|
BCNS
|
[NCBI]
|
2.07344e-05
|
|
|
OCA1A
|
[NCBI]
|
1.95691e-05
|
|
|
campomelic dysplasia
|
[NCBI]
|
1.95691e-05
|
|
|
CCL2
|
[NCBI]
|
1.94294e-05
|
|
|
DGS
|
[NCBI]
|
1.92224e-05
|
|
|
GAPDH
|
[NCBI]
|
1.91962e-05
|
|
|
FDH
|
[NCBI]
|
1.89185e-05
|
|
|
XPA
|
[NCBI]
|
1.89185e-05
|
|
|
SCS
|
[NCBI]
|
1.89185e-05
|
|
|
EGF
|
[NCBI]
|
1.89071e-05
|
|
|
TSHR
|
[NCBI]
|
1.87654e-05
|
|
|
LWD
|
[NCBI]
|
1.83007e-05
|
|
|
HSAN3
|
[NCBI]
|
1.80033e-05
|
|
|
SCIDX1
|
[NCBI]
|
1.80033e-05
|
|
|
KLK3
|
[NCBI]
|
1.74964e-05
|
|
|
AN2
|
[NCBI]
|
1.71528e-05
|
|
|
CLN3
|
[NCBI]
|
1.68824e-05
|
|
|
COL2A1
|
[NCBI]
|
1.62788e-05
|
|
|
PDS
|
[NCBI]
|
1.61069e-05
|
|
|
BPES
|
[NCBI]
|
1.58596e-05
|
|
|
GNAS
|
[NCBI]
|
1.56995e-05
|
|
|
STAR
|
[NCBI]
|
1.56995e-05
|
|
|
PTH
|
[NCBI]
|
1.56204e-05
|
|
|
BRRS
|
[NCBI]
|
1.49213e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
1.49213e-05
|
|
|
ABCB1
|
[NCBI]
|
1.48487e-05
|
|
|
ABL
|
[NCBI]
|
1.46985e-05
|
|
|
SCZD
|
[NCBI]
|
1.46985e-05
|
|
|
HOS
|
[NCBI]
|
1.46985e-05
|
|
|
GUSB
|
[NCBI]
|
1.46491e-05
|
|
|
RSTS
|
[NCBI]
|
1.44802e-05
|
|
|
BTK
|
[NCBI]
|
1.42638e-05
|
|
|
antithrombin iii deficiency
|
[NCBI]
|
1.40778e-05
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
1.28775e-05
|
|
|
HGPS
|
[NCBI]
|
1.18199e-05
|
|
|
BLM
|
[NCBI]
|
1.18199e-05
|
|
|
WRN
|
[NCBI]
|
1.13307e-05
|
|
|
FGFR2
|
[NCBI]
|
1.12502e-05
|
|
|
CFTR
|
[NCBI]
|
1.08445e-05
|
|
|
AMH
|
[NCBI]
|
1.05789e-05
|
|
|
WHS
|
[NCBI]
|
9.59435e-06
|
|
|
SDS
|
[NCBI]
|
9.59435e-06
|
|
|
HHT
|
[NCBI]
|
9.46369e-06
|
|
|
GJA1
|
[NCBI]
|
9.39954e-06
|
|
|
NS1
|
[NCBI]
|
8.71896e-06
|
|
|
PRNP
|
[NCBI]
|
7.90304e-06
|
|
|
SMS
|
[NCBI]
|
7.82046e-06
|
|
|
PRL
|
[NCBI]
|
7.40521e-06
|
|
|
PCNA
|
[NCBI]
|
6.94566e-06
|
|
|
RB1
|
[NCBI]
|
6.92358e-06
|
|
|
MAS
|
[NCBI]
|
6.37776e-06
|
|
|
IP
|
[NCBI]
|
5.11664e-06
|
|
|
HSCR1
|
[NCBI]
|
5.11664e-06
|
|
|
PWS
|
[NCBI]
|
5.01827e-06
|
|
|
EPO
|
[NCBI]
|
4.64282e-06
|
|
|
POMC
|
[NCBI]
|
4.39922e-06
|
|
|
NF1
|
[NCBI]
|
4.37867e-06
|
|
|
GFAP
|
[NCBI]
|
4.14359e-06
|
|
|
PF4
|
[NCBI]
|
3.8755e-06
|
|
|
PCD
|
[NCBI]
|
3.17439e-06
|
|
|
APOE
|
[NCBI]
|
2.97254e-06
|
|
|
AR
|
[NCBI]
|
2.2149e-06
|
|
|
WBS
|
[NCBI]
|
1.99241e-06
|
|
|
CHS
|
[NCBI]
|
1.92497e-06
|
|
|
PTHLH
|
[NCBI]
|
1.81869e-06
|
|
|
CHAT
|
[NCBI]
|
8.62379e-07
|
|
|
RTT
|
[NCBI]
|
6.93189e-07
|
|
|
HGF
|
[NCBI]
|
6.11647e-07
|
|
|
MUC1
|
[NCBI]
|
3.5218e-07
|
|
|
CAT
|
[NCBI]
|
1.21415e-07
|
|
|
polycystic kidneys
|
[NCBI]
|
1.19906e-07
|
|
|
AT
|
[NCBI]
|
8.65465e-09
|
|