|
OMIM |
Link |
Information gain |
01 |
|
OFC1
|
[NCBI]
|
0.0321032
|
|
|
CPI
|
[NCBI]
|
0.0164093
|
|
|
EEC1
|
[NCBI]
|
0.0090804
|
|
|
palatopharyngeal incompetence
|
[NCBI]
|
0.00682936
|
|
|
VWS
|
[NCBI]
|
0.00373271
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.00326551
|
|
|
OFC3
|
[NCBI]
|
0.00300167
|
|
|
blepharocheilodontic syndrome
|
[NCBI]
|
0.00290386
|
|
|
gordon syndrome
|
[NCBI]
|
0.00255989
|
|
|
OFC2
|
[NCBI]
|
0.00179871
|
|
|
aase-smith syndrome i
|
[NCBI]
|
0.00179871
|
|
|
CPX
|
[NCBI]
|
0.00157458
|
|
|
rosselli-gulienetti syndrome
|
[NCBI]
|
0.00144854
|
|
|
hypertelorism, microtia, facial clefting syndrome
|
[NCBI]
|
0.00144854
|
|
|
ocular hypotelorism, submucosal cleft palate, and hypospadias
|
[NCBI]
|
0.00119838
|
|
|
oculopalatocerebral syndrome
|
[NCBI]
|
0.00119838
|
|
|
pierre robin sequence with pectus excavatum and rib and scapular anomalies
|
[NCBI]
|
0.00115528
|
|
|
PPS
|
[NCBI]
|
0.00113888
|
|
|
OSCS
|
[NCBI]
|
0.00111761
|
|
|
dyssegmental dysplasia, rolland-desbuquois type
|
[NCBI]
|
0.000984017
|
|
|
velocardiofacial syndrome
|
[NCBI]
|
0.000964844
|
|
|
adducted thumbs syndrome
|
[NCBI]
|
0.000901652
|
|
|
orofacial cleft 4
|
[NCBI]
|
0.000901652
|
|
|
van der woude syndrome modifier
|
[NCBI]
|
0.000901652
|
|
|
IRF6
|
[NCBI]
|
0.000732131
|
|
|
POADS
|
[NCBI]
|
0.000729426
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000660402
|
|
|
FRNS
|
[NCBI]
|
0.00063791
|
|
|
acromelic frontonasal dysostosis
|
[NCBI]
|
0.000611929
|
|
|
van der woude syndrome 2
|
[NCBI]
|
0.000598811
|
|
|
diamond-blackfan anemia with microtia and cleft palate
|
[NCBI]
|
0.000598811
|
|
|
orofacial cleft 9
|
[NCBI]
|
0.000598811
|
|
|
broad terminal phalanges, familial
|
[NCBI]
|
0.000598811
|
|
|
armfield x-linked mental retardation syndrome
|
[NCBI]
|
0.000598811
|
|
|
RHS
|
[NCBI]
|
0.000583459
|
|
|
CLPED1
|
[NCBI]
|
0.000549918
|
|
|
popliteal pterygium syndrome, lethal type
|
[NCBI]
|
0.000512085
|
|
|
HFM
|
[NCBI]
|
0.000508733
|
|
|
THAS
|
[NCBI]
|
0.000439639
|
|
|
DA5
|
[NCBI]
|
0.000439639
|
|
|
RBS
|
[NCBI]
|
0.000401787
|
|
|
HFH
|
[NCBI]
|
0.000384369
|
|
|
cleft palate-lateral synechia syndrome
|
[NCBI]
|
0.000384369
|
|
|
ankyloblepharon-ectodermal defects-cleft lip/palate
|
[NCBI]
|
0.00036806
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000349466
|
|
|
constricting bands, congenital
|
[NCBI]
|
0.000337687
|
|
|
STL1
|
[NCBI]
|
0.000336516
|
|
|
TBX22
|
[NCBI]
|
0.000319525
|
|
|
MSX1
|
[NCBI]
|
0.000306269
|
|
|
DA4
|
[NCBI]
|
0.000305619
|
|
|
sprengel deformity
|
[NCBI]
|
0.000305619
|
|
|
OFD3
|
[NCBI]
|
0.000305619
|
|
|
immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum
|
[NCBI]
|
0.000305619
|
|
|
OFD5
|
[NCBI]
|
0.000305619
|
|
|
short rib-polydactyly syndrome, type ii
|
[NCBI]
|
0.000299623
|
|
|
hypothyroidism, athyroidal, with spiky hair and cleft palate
|
[NCBI]
|
0.000286366
|
|
|
TP73L
|
[NCBI]
|
0.000279107
|
|
|
PHF8
|
[NCBI]
|
0.000276965
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.000267226
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
0.000265121
|
|
|
OFD1
|
[NCBI]
|
0.000256863
|
|
|
adducted thumb-clubfoot syndrome
|
[NCBI]
|
0.000255713
|
|
|
OPD1
|
[NCBI]
|
0.000254869
|
|
|
SATB2
|
[NCBI]
|
0.000252103
|
|
|
microcephaly, corpus callosum dysgenesis, and cleft lip/palate
|
[NCBI]
|
0.000245074
|
|
|
coloboma, uveal, with cleft lip and palate and mental retardation
|
[NCBI]
|
0.000245074
|
|
|
siderius x-linked mental retardation syndrome
|
[NCBI]
|
0.000245074
|
|
|
DGS
|
[NCBI]
|
0.000244383
|
|
|
OPD2
|
[NCBI]
|
0.000242907
|
|
|
EEC3
|
[NCBI]
|
0.000242907
|
|
|
microtia-anotia
|
[NCBI]
|
0.000219506
|
|
|
VDEGS
|
[NCBI]
|
0.000219506
|
|
|
FOXE1
|
[NCBI]
|
0.000210118
|
|
|
say syndrome
|
[NCBI]
|
0.000208715
|
|
|
fryns microphthalmia syndrome
|
[NCBI]
|
0.000208715
|
|
|
orofacial cleft 5
|
[NCBI]
|
0.000208715
|
|
|
dubowitz syndrome
|
[NCBI]
|
0.000193139
|
|
|
OFD9
|
[NCBI]
|
0.000191368
|
|
|
malpuech facial clefting syndrome
|
[NCBI]
|
0.000190734
|
|
|
syndactyly, type i, with microcephaly and mental retardation
|
[NCBI]
|
0.000168561
|
|
|
MCOPS6
|
[NCBI]
|
0.000168561
|
|
|
short rib-polydactyly syndrome, type i
|
[NCBI]
|
0.000168561
|
|
|
STHAG4
|
[NCBI]
|
0.000168561
|
|
|
AIC
|
[NCBI]
|
0.000165095
|
|
|
holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate
|
[NCBI]
|
0.000163354
|
|
|
cleft palate, cardiac defect, genital anomalies, and ectrodactyly
|
[NCBI]
|
0.000163354
|
|
|
orofacial cleft 6
|
[NCBI]
|
0.000163354
|
|
|
PVRL1
|
[NCBI]
|
0.000150724
|
|
|
klippel-feil syndrome, autosomal dominant
|
[NCBI]
|
0.000149543
|
|
|
GABRB3
|
[NCBI]
|
0.000140619
|
|
|
OSR2
|
[NCBI]
|
0.000138338
|
|
|
LHX8
|
[NCBI]
|
0.000138338
|
|
|
hydrolethalus syndrome 1
|
[NCBI]
|
0.00013663
|
|
|
oculocerebrocutaneous syndrome
|
[NCBI]
|
0.00013663
|
|
|
FFS
|
[NCBI]
|
0.00013663
|
|
|
microtia with meatal atresia and conductive deafness
|
[NCBI]
|
0.000133359
|
|
|
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth
|
[NCBI]
|
0.000133359
|
|
|
genitopalatocardiac syndrome
|
[NCBI]
|
0.000132505
|
|
|
ankyloblepharon filiforme adnatum and cleft palate
|
[NCBI]
|
0.000132505
|
|
|
sakoda complex
|
[NCBI]
|
0.000132505
|
|
|
HPE2
|
[NCBI]
|
0.000128312
|
|
|
FOXC2
|
[NCBI]
|
0.000125384
|
|
|
LMS
|
[NCBI]
|
0.000124657
|
|
|
charge-like syndrome, x-linked
|
[NCBI]
|
0.00011862
|
|
|
FGFR1
|
[NCBI]
|
0.000116906
|
|
|
PDGFC
|
[NCBI]
|
0.000110795
|
|
|
holzgreve syndrome
|
[NCBI]
|
0.000109121
|
|
|
subglottic bar
|
[NCBI]
|
0.000109121
|
|
|
OFD4
|
[NCBI]
|
0.000107147
|
|
|
SUMO1
|
[NCBI]
|
0.000104915
|
|
|
FGFR2
|
[NCBI]
|
9.90851e-05
|
|
|
TGFB3
|
[NCBI]
|
9.67539e-05
|
|
|
DBQD
|
[NCBI]
|
9.63562e-05
|
|
|
goldberg-shprintzen megacolon syndrome
|
[NCBI]
|
9.59925e-05
|
|
|
KAL2
|
[NCBI]
|
9.49167e-05
|
|
|
SLC19A1
|
[NCBI]
|
9.36738e-05
|
|
|
FGF10
|
[NCBI]
|
9.10124e-05
|
|
|
catel-manzke syndrome
|
[NCBI]
|
8.68095e-05
|
|
|
skin creases, multiple benign ring-shaped, of limbs
|
[NCBI]
|
8.67611e-05
|
|
|
GAD1
|
[NCBI]
|
8.6576e-05
|
|
|
lymphedema, hereditary, ii
|
[NCBI]
|
8.30783e-05
|
|
|
mesomelic limb shortening and bowing
|
[NCBI]
|
8.16632e-05
|
|
|
arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
|
[NCBI]
|
8.16632e-05
|
|
|
oculomaxillofacial dysplasia with oblique facial clefts
|
[NCBI]
|
8.16632e-05
|
|
|
brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia
|
[NCBI]
|
8.16632e-05
|
|
|
megaepiphyseal dwarfism
|
[NCBI]
|
8.16632e-05
|
|
|
midline malformations, multiple, with limb abnormalities and hypopituitarism
|
[NCBI]
|
8.16632e-05
|
|
|
crumpled helices and small mouth
|
[NCBI]
|
8.16632e-05
|
|
|
omphalocele-cleft palate syndrome, lethal
|
[NCBI]
|
8.16632e-05
|
|
|
lissencephaly, familial, with cleft palate and cerebellar hypoplasia
|
[NCBI]
|
8.16632e-05
|
|
|
pierre robin sequence with facial and digital anomalies
|
[NCBI]
|
8.16632e-05
|
|
|
parc syndrome
|
[NCBI]
|
8.16632e-05
|
|
|
cleft lip, congenital healed
|
[NCBI]
|
8.16632e-05
|
|
|
median-ulnar nerve communications
|
[NCBI]
|
8.16632e-05
|
|
|
multiple epiphyseal dysplasia with robin phenotype
|
[NCBI]
|
8.16632e-05
|
|
|
cleft soft palate
|
[NCBI]
|
8.16632e-05
|
|
|
arthrogryposis, distal, with peculiar facies and hydronephrosis
|
[NCBI]
|
8.16632e-05
|
|
|
palant cleft palate syndrome
|
[NCBI]
|
8.16632e-05
|
|
|
cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss
|
[NCBI]
|
8.16632e-05
|
|
|
rudiger syndrome
|
[NCBI]
|
8.16632e-05
|
|
|
ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin
|
[NCBI]
|
8.16632e-05
|
|
|
radius, aplasia of, with cleft lip/palate
|
[NCBI]
|
8.16632e-05
|
|
|
spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation
|
[NCBI]
|
8.16632e-05
|
|
|
brachioskeletogenital syndrome
|
[NCBI]
|
8.16632e-05
|
|
|
cerebrorenodigital syndrome with limb malformations and triradiate acetabula
|
[NCBI]
|
8.16632e-05
|
|
|
coloboma of macula and skeletal anomalies
|
[NCBI]
|
8.16632e-05
|
|
|
growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate
|
[NCBI]
|
8.16632e-05
|
|
|
macrosomia with microphthalmia, lethal
|
[NCBI]
|
8.16632e-05
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
7.92149e-05
|
|
|
DWS
|
[NCBI]
|
7.87718e-05
|
|
|
mohr syndrome
|
[NCBI]
|
7.81775e-05
|
|
|
branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging
|
[NCBI]
|
7.81775e-05
|
|
|
LDS
|
[NCBI]
|
7.40377e-05
|
|
|
adult syndrome
|
[NCBI]
|
7.40377e-05
|
|
|
DA2B
|
[NCBI]
|
7.15424e-05
|
|
|
WHS
|
[NCBI]
|
6.99508e-05
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
6.92405e-05
|
|
|
WGN1
|
[NCBI]
|
6.92405e-05
|
|
|
kniest dysplasia
|
[NCBI]
|
6.92405e-05
|
|
|
CLDN5
|
[NCBI]
|
6.91328e-05
|
|
|
npl4, s. cerevisiae, homolog of
|
[NCBI]
|
6.91328e-05
|
|
|
MSC
|
[NCBI]
|
6.91328e-05
|
|
|
CLPTM1
|
[NCBI]
|
6.91328e-05
|
|
|
ARVCF
|
[NCBI]
|
6.91328e-05
|
|
|
KLHL4
|
[NCBI]
|
6.91328e-05
|
|
|
TGFBR2
|
[NCBI]
|
6.84717e-05
|
|
|
SLOS
|
[NCBI]
|
6.61978e-05
|
|
|
SHH
|
[NCBI]
|
6.51103e-05
|
|
|
FGF8
|
[NCBI]
|
6.30249e-05
|
|
|
COMT
|
[NCBI]
|
6.05966e-05
|
|
|
crane-heise syndrome
|
[NCBI]
|
5.9296e-05
|
|
|
pallister w syndrome
|
[NCBI]
|
5.9296e-05
|
|
|
lymphedema and ptosis
|
[NCBI]
|
5.9296e-05
|
|
|
pierre robin syndrome and oligodactyly
|
[NCBI]
|
5.9296e-05
|
|
|
acrofrontofacionasal dysostosis syndrome
|
[NCBI]
|
5.9296e-05
|
|
|
arthrogryposis, distal, type 2e
|
[NCBI]
|
5.9296e-05
|
|
|
dk phocomelia syndrome
|
[NCBI]
|
5.9296e-05
|
|
|
ectrodactyly-cleft palate syndrome
|
[NCBI]
|
5.9296e-05
|
|
|
telecanthus
|
[NCBI]
|
5.9296e-05
|
|
|
hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation
|
[NCBI]
|
5.9296e-05
|
|
|
craniosynostosis with fibular aplasia
|
[NCBI]
|
5.9296e-05
|
|
|
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
|
[NCBI]
|
5.9296e-05
|
|
|
OFD7
|
[NCBI]
|
5.9296e-05
|
|
|
cleft lip/palate with characteristic facies, intestinal malrotation, and lethal congenital heart disease
|
[NCBI]
|
5.9296e-05
|
|
|
dextrocardia with unusual facies and microphthalmia
|
[NCBI]
|
5.9296e-05
|
|
|
faciocardiorenal syndrome
|
[NCBI]
|
5.9296e-05
|
|
|
lymphedema-distichiasis syndrome
|
[NCBI]
|
5.68165e-05
|
|
|
AFD1
|
[NCBI]
|
5.54124e-05
|
|
|
MNS
|
[NCBI]
|
5.54124e-05
|
|
|
ALPI
|
[NCBI]
|
5.53615e-05
|
|
|
MNT
|
[NCBI]
|
5.53615e-05
|
|
|
twirler mutation, murine, human homolog of
|
[NCBI]
|
5.53615e-05
|
|
|
TBX10
|
[NCBI]
|
5.53615e-05
|
|
|
DBA
|
[NCBI]
|
5.38254e-05
|
|
|
TCOF
|
[NCBI]
|
5.32202e-05
|
|
|
diastrophic dysplasia
|
[NCBI]
|
5.15813e-05
|
|
|
hydrocephalus with cerebellar agenesis
|
[NCBI]
|
5.09193e-05
|
|
|
chands
|
[NCBI]
|
5.09193e-05
|
|
|
split-foot deformity with mandibulofacial dysostosis
|
[NCBI]
|
5.09193e-05
|
|
|
lowry-maclean syndrome
|
[NCBI]
|
5.09193e-05
|
|
|
albinism, ocular, with sensorineural deafness
|
[NCBI]
|
5.09193e-05
|
|
|
brachial amelia, forebrain defects, and facial clefts
|
[NCBI]
|
5.09193e-05
|
|
|
carnevale syndrome
|
[NCBI]
|
5.09193e-05
|
|
|
cree mental retardation syndrome
|
[NCBI]
|
5.09193e-05
|
|
|
myopathy, congenital nonprogressive, with moebius sequence and robin sequence
|
[NCBI]
|
5.09193e-05
|
|
|
omphalocele, diaphragmatic hernia, and radial ray defects
|
[NCBI]
|
5.09193e-05
|
|
|
KPC
|
[NCBI]
|
5.09193e-05
|
|
|
SLC25A1
|
[NCBI]
|
5.01695e-05
|
|
|
ARNT2
|
[NCBI]
|
5.01695e-05
|
|
|
TCF21
|
[NCBI]
|
5.01695e-05
|
|
|
IGFBP2
|
[NCBI]
|
5.01695e-05
|
|
|
SNX3
|
[NCBI]
|
5.01695e-05
|
|
|
JAG2
|
[NCBI]
|
5.01695e-05
|
|
|
MTHFR
|
[NCBI]
|
4.95518e-05
|
|
|
COL2A1
|
[NCBI]
|
4.68407e-05
|
|
|
DLG1
|
[NCBI]
|
4.68011e-05
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
4.62408e-05
|
|
|
brachycephaly, deafness, cataract, microstomia, and mental retardation
|
[NCBI]
|
4.55164e-05
|
|
|
CRS2
|
[NCBI]
|
4.55164e-05
|
|
|
coloboma of macula with type b brachydactyly
|
[NCBI]
|
4.55164e-05
|
|
|
aminopterin syndrome sine aminopterin
|
[NCBI]
|
4.55164e-05
|
|
|
MCOPS8
|
[NCBI]
|
4.55164e-05
|
|
|
pierre robin syndrome
|
[NCBI]
|
4.55164e-05
|
|
|
tetra-amelia, autosomal recessive
|
[NCBI]
|
4.55164e-05
|
|
|
oculopalatoskeletal syndrome
|
[NCBI]
|
4.55164e-05
|
|
|
CHRND
|
[NCBI]
|
4.42988e-05
|
|
|
IGFBP5
|
[NCBI]
|
4.42988e-05
|
|
|
ESCO2
|
[NCBI]
|
4.42988e-05
|
|
|
AHR
|
[NCBI]
|
4.30176e-05
|
|
|
DA2A
|
[NCBI]
|
4.25559e-05
|
|
|
ICSBP1
|
[NCBI]
|
4.23067e-05
|
|
|
cutis gyrata syndrome of beare and stevenson
|
[NCBI]
|
4.15259e-05
|
|
|
yellow nail syndrome
|
[NCBI]
|
4.15259e-05
|
|
|
keratitis, hereditary
|
[NCBI]
|
4.15259e-05
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
4.14869e-05
|
|
|
SEDC
|
[NCBI]
|
4.09129e-05
|
|
|
apert syndrome
|
[NCBI]
|
4.09129e-05
|
|
|
AGC1
|
[NCBI]
|
4.06516e-05
|
|
|
charge syndrome
|
[NCBI]
|
4.01296e-05
|
|
|
UBB
|
[NCBI]
|
3.92361e-05
|
|
|
stickler syndrome, type i, nonsyndromic ocular
|
[NCBI]
|
3.83673e-05
|
|
|
STHAG1
|
[NCBI]
|
3.83673e-05
|
|
|
fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly
|
[NCBI]
|
3.83673e-05
|
|
|
tibial hemimelia
|
[NCBI]
|
3.83673e-05
|
|
|
cleft larynx, posterior
|
[NCBI]
|
3.83673e-05
|
|
|
aglossia-adactylia
|
[NCBI]
|
3.83673e-05
|
|
|
zunich neuroectodermal syndrome
|
[NCBI]
|
3.83673e-05
|
|
|
EFNB1
|
[NCBI]
|
3.79997e-05
|
|
|
walker-warburg syndrome
|
[NCBI]
|
3.79174e-05
|
|
|
PAX9
|
[NCBI]
|
3.69024e-05
|
|
|
GSK3B
|
[NCBI]
|
3.69024e-05
|
|
|
kabuki syndrome
|
[NCBI]
|
3.60045e-05
|
|
|
BHMT
|
[NCBI]
|
3.59161e-05
|
|
|
PHS
|
[NCBI]
|
3.58881e-05
|
|
|
pseudodiastrophic dysplasia
|
[NCBI]
|
3.57583e-05
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
3.354e-05
|
|
|
murcs association
|
[NCBI]
|
3.354e-05
|
|
|
frontonasal dysplasia
|
[NCBI]
|
3.354e-05
|
|
|
phace association
|
[NCBI]
|
3.354e-05
|
|
|
COL11A2
|
[NCBI]
|
3.34447e-05
|
|
|
COL11A1
|
[NCBI]
|
3.34447e-05
|
|
|
HSD11B1
|
[NCBI]
|
3.34447e-05
|
|
|
cayler cardiofacial syndrome
|
[NCBI]
|
3.31836e-05
|
|
|
peters-plus syndrome
|
[NCBI]
|
3.16138e-05
|
|
|
PQBP1
|
[NCBI]
|
3.14775e-05
|
|
|
CES
|
[NCBI]
|
3.11979e-05
|
|
|
FN1
|
[NCBI]
|
3.09019e-05
|
|
|
KNO
|
[NCBI]
|
2.99144e-05
|
|
|
lenz-majewski hyperostotic dwarfism
|
[NCBI]
|
2.99144e-05
|
|
|
trismus-pseudocamptodactyly syndrome
|
[NCBI]
|
2.99144e-05
|
|
|
EYA1
|
[NCBI]
|
2.93571e-05
|
|
|
EDN1
|
[NCBI]
|
2.84504e-05
|
|
|
DA1
|
[NCBI]
|
2.8396e-05
|
|
|
sc phocomelia syndrome
|
[NCBI]
|
2.8396e-05
|
|
|
SCZD4
|
[NCBI]
|
2.8396e-05
|
|
|
OSMED
|
[NCBI]
|
2.8396e-05
|
|
|
RARA
|
[NCBI]
|
2.80275e-05
|
|
|
MKS1
|
[NCBI]
|
2.73158e-05
|
|
|
WS3
|
[NCBI]
|
2.70258e-05
|
|
|
SOX9
|
[NCBI]
|
2.65026e-05
|
|
|
RB1
|
[NCBI]
|
2.64267e-05
|
|
|
FGFR3
|
[NCBI]
|
2.64267e-05
|
|
|
ARX
|
[NCBI]
|
2.6157e-05
|
|
|
FRA16A
|
[NCBI]
|
2.57788e-05
|
|
|
WZS
|
[NCBI]
|
2.57788e-05
|
|
|
disorganization, mouse, homolog of
|
[NCBI]
|
2.57788e-05
|
|
|
RNS
|
[NCBI]
|
2.57788e-05
|
|
|
RENS1
|
[NCBI]
|
2.57788e-05
|
|
|
LADD
|
[NCBI]
|
2.57788e-05
|
|
|
REN
|
[NCBI]
|
2.51904e-05
|
|
|
ACG2
|
[NCBI]
|
2.4636e-05
|
|
|
MCOPS2
|
[NCBI]
|
2.4636e-05
|
|
|
FLNA
|
[NCBI]
|
2.37731e-05
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
2.35826e-05
|
|
|
PFM
|
[NCBI]
|
2.35826e-05
|
|
|
LRS1
|
[NCBI]
|
2.26066e-05
|
|
|
CDH1
|
[NCBI]
|
2.10608e-05
|
|
|
DRRS
|
[NCBI]
|
2.08495e-05
|
|
|
FMD
|
[NCBI]
|
2.08495e-05
|
|
|
NLS
|
[NCBI]
|
2.04596e-05
|
|
|
HS
|
[NCBI]
|
1.8378e-05
|
|
|
MTR
|
[NCBI]
|
1.8378e-05
|
|
|
IHH
|
[NCBI]
|
1.75505e-05
|
|
|
ABCB1
|
[NCBI]
|
1.53581e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
1.41024e-05
|
|
|
PTH
|
[NCBI]
|
1.40372e-05
|
|
|
CFNS
|
[NCBI]
|
1.36487e-05
|
|
|
CHNG2
|
[NCBI]
|
1.32138e-05
|
|
|
faciogenital dysplasia
|
[NCBI]
|
1.32138e-05
|
|
|
BOR1
|
[NCBI]
|
1.27962e-05
|
|
|
fraser syndrome
|
[NCBI]
|
1.27962e-05
|
|
|
MCOPS7
|
[NCBI]
|
1.23951e-05
|
|
|
SGBS1
|
[NCBI]
|
1.20092e-05
|
|
|
MDLS
|
[NCBI]
|
1.12801e-05
|
|
|
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity
|
[NCBI]
|
1.09353e-05
|
|
|
MEB
|
[NCBI]
|
1.06026e-05
|
|
|
OCA1A
|
[NCBI]
|
9.10093e-06
|
|
|
campomelic dysplasia
|
[NCBI]
|
9.10093e-06
|
|
|
EGF
|
[NCBI]
|
8.77812e-06
|
|
|
SCS
|
[NCBI]
|
8.56644e-06
|
|
|
CVID
|
[NCBI]
|
6.97424e-06
|
|
|
holoprosencephaly
|
[NCBI]
|
5.7858e-06
|
|
|
WS1
|
[NCBI]
|
5.2752e-06
|
|
|
BCNS
|
[NCBI]
|
4.70326e-06
|
|
|
GNRH1
|
[NCBI]
|
4.47251e-06
|
|
|
AMC
|
[NCBI]
|
4.10611e-06
|
|
|
NPS
|
[NCBI]
|
4.10611e-06
|
|
|
PSACH
|
[NCBI]
|
3.49166e-06
|
|
|
hypogonadotropic hypogonadism
|
[NCBI]
|
2.47914e-06
|
|
|
SHFM1
|
[NCBI]
|
2.17571e-06
|
|
|
AVP
|
[NCBI]
|
1.60072e-06
|
|
|
NS1
|
[NCBI]
|
1.44408e-06
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
1.07091e-06
|
|
|
SMS
|
[NCBI]
|
1.01022e-06
|
|
|
EGFR
|
[NCBI]
|
8.89849e-07
|
|
|
PCNA
|
[NCBI]
|
4.26122e-07
|
|
|
ACHE
|
[NCBI]
|
2.35588e-07
|
|
|
BWS
|
[NCBI]
|
8.45719e-09
|
|