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MeSH keywords -> Related genes, diseases (OMIM)


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01 Cleft Palate [NCBI]


Gene


Gene Link Information
Gain
01
AFA [NCBI] 0.00101904
VCF [NCBI] 0.000865656
OFC3 [NCBI] 0.000640741
OFC4 [NCBI] 0.000640741
IRF6 [NCBI] 0.000615099
HFM [NCBI] 0.000488483
CAPZA1P [NCBI] 0.000319375
VWS2 [NCBI] 0.000319375
XCE [NCBI] 0.000319375
MRXSA [NCBI] 0.000319375
TW [NCBI] 0.000319375
OFC2 [NCBI] 0.000319375
EEC2 [NCBI] 0.000319375
EEC1 [NCBI] 0.000319375
DGCR [NCBI] 0.000235759
MSX1 [NCBI] 0.000219086
SCZD4 [NCBI] 0.000193754
TBX22 [NCBI] 0.000176642
TGFA [NCBI] 0.000135253
TGFB3 [NCBI] 0.000117192
TP63 [NCBI] 0.000108386
PVRL1 [NCBI] 9.96267e-05
FOXE1 [NCBI] 7.87305e-05
MTHFR [NCBI] 7.60128e-05
PHF8 [NCBI] 6.78279e-05
GABRB3 [NCBI] 5.38934e-05
BMP2 [NCBI] 5.00272e-05
SATB2 [NCBI] 4.99555e-05
BMP4 [NCBI] 4.14842e-05
SUMO1 [NCBI] 4.06987e-05
TBX10 [NCBI] 4.06802e-05
FGFR1 [NCBI] 4.06635e-05
RFC1 [NCBI] 3.86127e-05
LHX8 [NCBI] 3.68183e-05
CLPTM1 [NCBI] 3.49031e-05
ARVCF [NCBI] 3.15952e-05
PAX9 [NCBI] 3.00664e-05
NAT1 [NCBI] 2.78874e-05
RARA [NCBI] 2.7767e-05
GSTT1 [NCBI] 2.76617e-05
CKAP4 [NCBI] 2.48714e-05
MTRR [NCBI] 2.24924e-05
TGFBR1 [NCBI] 2.2397e-05
COL2A1 [NCBI] 2.236e-05
KLHL4 [NCBI] 2.23549e-05
DLX3 [NCBI] 2.1016e-05
BARX1 [NCBI] 2.05592e-05
GSTM1 [NCBI] 2.03107e-05
FOXC2 [NCBI] 1.95317e-05
FGF18 [NCBI] 1.93934e-05
TTF2 [NCBI] 1.8527e-05
PVRL2 [NCBI] 1.75378e-05
SPRY2 [NCBI] 1.59616e-05
CYP1A1 [NCBI] 1.58401e-05
BCL3 [NCBI] 1.5786e-05
GAD1 [NCBI] 1.54597e-05
MTR [NCBI] 1.52237e-05
EPHX1 [NCBI] 1.51918e-05
CHD7 [NCBI] 1.51619e-05
NAT2 [NCBI] 1.47338e-05
FGFR2 [NCBI] 1.42384e-05
SKI [NCBI] 1.37765e-05
MTHFD1 [NCBI] 1.35921e-05
FAM120C [NCBI] 1.35546e-05
DPF3 [NCBI] 1.35546e-05
NPLOC4 [NCBI] 1.35546e-05
COL27A1 [NCBI] 1.35546e-05
CRISPLD2 [NCBI] 1.35546e-05
OFCC1 [NCBI] 1.35546e-05
CPXCR1 [NCBI] 1.35546e-05
SCN3B [NCBI] 1.35546e-05
PDGFC [NCBI] 1.31706e-05
FGF10 [NCBI] 1.30157e-05
GLI2 [NCBI] 1.27258e-05
SHH [NCBI] 1.15006e-05
AHR [NCBI] 1.1325e-05
RPS19 [NCBI] 1.12804e-05
MTRF1L [NCBI] 1.11747e-05
C6orf211 [NCBI] 1.11747e-05
CAMK1G [NCBI] 1.11747e-05
IMP5 [NCBI] 1.11747e-05
VAX2 [NCBI] 1.11747e-05
OSR2 [NCBI] 1.11747e-05
C6orf105 [NCBI] 1.11747e-05
MYH9 [NCBI] 1.07783e-05
SLC19A2 [NCBI] 1.07783e-05
PVR [NCBI] 1.03764e-05
RSPO3 [NCBI] 1.02768e-05
RWDD1 [NCBI] 1.02768e-05
UNQ1887 [NCBI] 1.02768e-05
NRXN3 [NCBI] 1.02768e-05
YAF2 [NCBI] 1.02768e-05
WNT9B [NCBI] 1.02768e-05
SHOX2 [NCBI] 1.02768e-05
HOXA2 [NCBI] 1.02768e-05
RPL36 [NCBI] 1.02768e-05
KIAA1279 [NCBI] 1.02768e-05
ADH1C [NCBI] 1.02415e-05
BHMT2 [NCBI] 9.69399e-06
WNT8A [NCBI] 9.69399e-06
SASH1 [NCBI] 9.69399e-06
EPHB3 [NCBI] 9.69399e-06
AKAP2 [NCBI] 9.69399e-06
WNT11 [NCBI] 9.69399e-06
RPS7 [NCBI] 9.69399e-06
WNK3 [NCBI] 9.69399e-06
MTHFD1L [NCBI] 9.69399e-06
PDSS2 [NCBI] 9.69399e-06
SNX3 [NCBI] 9.69399e-06
FOXL1 [NCBI] 9.69399e-06
TNS1 [NCBI] 9.26075e-06
WNT10A [NCBI] 9.26075e-06
PRUNE [NCBI] 9.26075e-06
G0S2 [NCBI] 9.26075e-06
GIPC2 [NCBI] 9.26075e-06
RPS15 [NCBI] 9.26075e-06
WSB1 [NCBI] 9.26075e-06
RPS17 [NCBI] 9.26075e-06
RPL11 [NCBI] 9.26075e-06
PKN2 [NCBI] 9.26075e-06
CBS [NCBI] 9.03789e-06
GDF6 [NCBI] 8.91562e-06
SLC2A12 [NCBI] 8.91562e-06
ARNT2 [NCBI] 8.91562e-06
MMP25 [NCBI] 8.91562e-06
SLC12A5 [NCBI] 8.91562e-06
WNT6 [NCBI] 8.91562e-06
GSC [NCBI] 8.62873e-06
GABBR2 [NCBI] 8.62873e-06
ESCO2 [NCBI] 8.62873e-06
AUH [NCBI] 8.62873e-06
ZNF202 [NCBI] 8.62873e-06
EGF [NCBI] 8.43785e-06
RYK [NCBI] 8.38322e-06
OSR1 [NCBI] 8.38322e-06
RPS27A [NCBI] 8.16865e-06
TAAR6 [NCBI] 8.16865e-06
BAG4 [NCBI] 8.16865e-06
PTPN3 [NCBI] 8.16865e-06
TGFB2 [NCBI] 8.02474e-06
TCF21 [NCBI] 7.9781e-06
GART [NCBI] 7.9781e-06
WNT3 [NCBI] 7.80673e-06
FBP1 [NCBI] 7.65105e-06
SLC7A11 [NCBI] 7.65105e-06
CHRND [NCBI] 7.65105e-06
RPL5 [NCBI] 7.65105e-06
WNT3A [NCBI] 7.65105e-06
FGF7 [NCBI] 7.57382e-06
IKZF3 [NCBI] 7.50843e-06
TCN1 [NCBI] 7.50843e-06
MYH14 [NCBI] 7.50843e-06
LAMA4 [NCBI] 7.50843e-06
AHCY [NCBI] 7.50843e-06
OSTM1 [NCBI] 7.50843e-06
MLPH [NCBI] 7.50843e-06
FBXW4 [NCBI] 7.37684e-06
COL11A1 [NCBI] 7.37684e-06
SNAI2 [NCBI] 7.29659e-06
OFD1 [NCBI] 7.03405e-06
ACVR2A [NCBI] 7.03405e-06
JAG2 [NCBI] 7.03405e-06
FZD7 [NCBI] 6.93362e-06
BMP7 [NCBI] 6.87537e-06
NEK2 [NCBI] 6.83881e-06
PRRX1 [NCBI] 6.83881e-06
MSX2 [NCBI] 6.83881e-06
FST [NCBI] 6.83881e-06
HSF2 [NCBI] 6.83881e-06
ALX4 [NCBI] 6.74903e-06
GSTP1 [NCBI] 6.66905e-06
KIF21A [NCBI] 6.66378e-06
MID1 [NCBI] 6.58262e-06
HOXA1 [NCBI] 6.58262e-06
TGFBR3 [NCBI] 6.50518e-06
RAI1 [NCBI] 6.50518e-06
SCN2A [NCBI] 6.50518e-06
DFNA5 [NCBI] 6.3602e-06
UFD1L [NCBI] 6.29214e-06
HS3ST5 [NCBI] 6.29214e-06
FZD4 [NCBI] 6.22672e-06
WNT7A [NCBI] 6.22672e-06
TCN2 [NCBI] 6.22672e-06
DLX4 [NCBI] 6.16374e-06
EFNB1 [NCBI] 6.10304e-06
HDAC4 [NCBI] 6.04446e-06
FGF1 [NCBI] 6.04446e-06
ACAN [NCBI] 5.93309e-06
BHMT [NCBI] 5.88006e-06
CRHR1 [NCBI] 5.73035e-06
SDC2 [NCBI] 5.68329e-06
CLDN5 [NCBI] 5.63751e-06
FOLR1 [NCBI] 5.57626e-06
COL4A4 [NCBI] 5.46602e-06
SP100 [NCBI] 5.46602e-06
FBLN1 [NCBI] 5.42577e-06
TCOF1 [NCBI] 5.31056e-06
FLNA [NCBI] 5.27387e-06
COL4A3 [NCBI] 5.23797e-06
TBX1 [NCBI] 5.16843e-06
LEF1 [NCBI] 4.91628e-06
HAPLN1 [NCBI] 4.80336e-06
IRF8 [NCBI] 4.74968e-06
CDH2 [NCBI] 4.69771e-06
COMT [NCBI] 4.61462e-06
REN [NCBI] 4.55104e-06
FGF8 [NCBI] 4.55104e-06
SCN1A [NCBI] 4.46013e-06
HSD11B1 [NCBI] 4.46013e-06
INHBA [NCBI] 4.33265e-06
GPC3 [NCBI] 4.33265e-06
FGA [NCBI] 4.33265e-06
WNT5A [NCBI] 4.25293e-06
UCP1 [NCBI] 4.08683e-06
COL11A2 [NCBI] 4.0015e-06
STAT5B [NCBI] 3.93637e-06
APEX1 [NCBI] 3.93637e-06
PDGFRA [NCBI] 3.90479e-06
FOXO3 [NCBI] 3.82847e-06
LIPC [NCBI] 3.79895e-06
FGF3 [NCBI] 3.61949e-06
RUNX2 [NCBI] 3.6065e-06
EPB41L1 [NCBI] 3.58085e-06
CYP1A2 [NCBI] 3.58085e-06
CTNND1 [NCBI] 3.49424e-06
ARNT [NCBI] 3.45856e-06
NPPB [NCBI] 3.42368e-06
EPB41L2 [NCBI] 3.41223e-06
SOX9 [NCBI] 3.40086e-06
NOG [NCBI] 3.40086e-06
NGFR [NCBI] 3.40086e-06
FYN [NCBI] 3.38958e-06
TWIST1 [NCBI] 3.26026e-06
OGG1 [NCBI] 3.1995e-06
XRCC3 [NCBI] 3.1995e-06
TP73 [NCBI] 3.14108e-06
CDKN1C [NCBI] 3.02178e-06
CYP1B1 [NCBI] 2.79334e-06
MMP3 [NCBI] 2.74869e-06
CYP2E1 [NCBI] 2.64274e-06
PAX3 [NCBI] 2.61576e-06
CREBBP [NCBI] 2.53774e-06
IRF1 [NCBI] 2.53143e-06
MMP1 [NCBI] 2.50029e-06
CD44 [NCBI] 2.47586e-06
ADAM17 [NCBI] 2.45781e-06
EGFR [NCBI] 2.45136e-06
ITGB3 [NCBI] 2.26815e-06
PAX6 [NCBI] 2.23724e-06
PCNA [NCBI] 2.20758e-06
PDGFA [NCBI] 2.1971e-06
ERBB4 [NCBI] 2.1726e-06
PGF [NCBI] 2.1296e-06
XRCC1 [NCBI] 1.95796e-06
PRKCB [NCBI] 1.90545e-06
ERCC2 [NCBI] 1.83615e-06
MMP2 [NCBI] 1.65529e-06
CDH1 [NCBI] 1.64243e-06
ERBB2 [NCBI] 1.37774e-06
MMP9 [NCBI] 1.34034e-06
MAPT [NCBI] 1.30656e-06
STAT1 [NCBI] 1.16673e-06
CDK2 [NCBI] 1.08132e-06
TLR4 [NCBI] 5.16373e-07
STAT3 [NCBI] 4.20786e-07
ACHE [NCBI] 3.68565e-07
NOS3 [NCBI] 2.93744e-07
PTH [NCBI] 1.55509e-07
CDKN1A [NCBI] 6.2628e-08
TGFB1 [NCBI] 5.33096e-08




OMIM


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




Database Center for Life Science