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01 Craniosynostoses [NCBI]

Gene


 Gene Link Information
Gain		 01
CRS [NCBI] 0.000771147
FGFR3 [NCBI] 0.000619948
FGFR2 [NCBI] 0.000429116
CDAGS [NCBI] 0.000381162
CRSA [NCBI] 0.000381162
TWIST1 [NCBI] 0.000343312
OSCS [NCBI] 0.000320423
FND [NCBI] 0.000262737
FGFR1 [NCBI] 7.56374e-05
MSX2 [NCBI] 6.64752e-05
POR [NCBI] 6.41555e-05
EFNB1 [NCBI] 6.14387e-05
NOG [NCBI] 5.32998e-05
NELL1 [NCBI] 4.62867e-05
TGFBR1 [NCBI] 2.67971e-05
RECQL4 [NCBI] 2.50838e-05
RUNX2 [NCBI] 1.90281e-05
FGF2 [NCBI] 1.76487e-05
BMP2 [NCBI] 1.72746e-05
SNAI2 [NCBI] 1.55959e-05
SNAI1 [NCBI] 1.53699e-05
C1QTNF3 [NCBI] 1.20663e-05
FGF4 [NCBI] 1.19368e-05
CDON [NCBI] 1.11682e-05
ENPP1 [NCBI] 1.04785e-05
EFNA4 [NCBI] 1.01516e-05
EFNA2 [NCBI] 9.80617e-06
IBSP [NCBI] 9.76102e-06
SOX6 [NCBI] 9.27324e-06
TWIST2 [NCBI] 9.27324e-06
EPHA4 [NCBI] 8.39716e-06
DLX5 [NCBI] 7.63594e-06
TCIRG1 [NCBI] 7.31701e-06
FGF9 [NCBI] 7.17749e-06
WIF1 [NCBI] 6.92877e-06
TCOF1 [NCBI] 6.19072e-06
FLNA [NCBI] 6.15377e-06
TCF3 [NCBI] 5.62517e-06
FGF8 [NCBI] 5.42445e-06
FGFR4 [NCBI] 5.24537e-06
JUN [NCBI] 4.61766e-06
PAX2 [NCBI] 4.53298e-06
FBN1 [NCBI] 4.51929e-06
FGF3 [NCBI] 4.47888e-06
CYP1A2 [NCBI] 4.43946e-06
ID1 [NCBI] 4.18752e-06
JAG1 [NCBI] 3.74435e-06
BMP4 [NCBI] 3.5034e-06
SMAD2 [NCBI] 3.35913e-06
BMP7 [NCBI] 3.15103e-06
DMPK [NCBI] 2.88929e-06
MECP2 [NCBI] 2.48909e-06
CASP9 [NCBI] 1.28648e-06
PLAUR [NCBI] 1.28371e-06
TRH [NCBI] 1.21545e-06
TGFB1 [NCBI] 4.08841e-07
BAX [NCBI] 3.82492e-07
CASP3 [NCBI] 1.0243e-07
EGF [NCBI] 1.09089e-09



OMIM


 OMIM Link Information
gain		 01
BGS [NCBI] 0.00201402
FGFR2 [NCBI] 0.00198725
CRSA [NCBI] 0.00197839
cdags syndrome [NCBI] 0.00197839
ABS [NCBI] 0.00176673
CFNS [NCBI] 0.00133548
hypertelorism, teebi type [NCBI] 0.00132132
cranioectodermal dysplasia [NCBI] 0.00127273
FGFR3 [NCBI] 0.00123837
JWS [NCBI] 0.000924043
CRS1 [NCBI] 0.000864599
SCS [NCBI] 0.000835993
hypomandibular faciocranial dysostosis [NCBI] 0.000766909
muenke syndrome [NCBI] 0.000701009
sprengel deformity [NCBI] 0.000684933
shprintzen-goldberg craniosynostosis syndrome [NCBI] 0.000677681
MCOPS4 [NCBI] 0.0006318
SGM1 [NCBI] 0.0006318
prognathism, mandibular [NCBI] 0.000561
acromelic frontonasal dysostosis [NCBI] 0.000561
OSCS [NCBI] 0.000561
MCOPS6 [NCBI] 0.000534964
c syndrome [NCBI] 0.000516332
hennekam lymphangiectasia-lymphedema syndrome [NCBI] 0.000512719
pfeiffer syndrome [NCBI] 0.000486722
ear, patella, short stature syndrome [NCBI] 0.000476092
MCOP1 [NCBI] 0.000476092
MCOPS1 [NCBI] 0.000460635
trigonocephaly, nonsyndromic [NCBI] 0.000390421
craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis [NCBI] 0.000390421
por deficiency [NCBI] 0.000376045
MSX2 [NCBI] 0.00036325
dubowitz syndrome [NCBI] 0.000337721
carpenter syndrome [NCBI] 0.000313045
crouzon syndrome [NCBI] 0.000306481
TWIST1 [NCBI] 0.000299064
furlong syndrome: fs [NCBI] 0.000256279
craniosynostosis with ectopia lentis [NCBI] 0.000256279
CRS2 [NCBI] 0.000256279
apert syndrome [NCBI] 0.00025192
hunter-mcalpine craniosynostosis syndrome [NCBI] 0.000238232
POR [NCBI] 0.00022508
FGFR1 [NCBI] 0.000222732
trigonocephaly with short stature and developmental delay [NCBI] 0.000195061
craniosynostosis-mental retardation syndrome of lin and gettig [NCBI] 0.000195061
craniomicromelic syndrome [NCBI] 0.000195061
kleeblattschaedel syndrome [NCBI] 0.000195061
craniosynostosis with fibular aplasia [NCBI] 0.000195061
lowry-maclean syndrome [NCBI] 0.000164145
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features [NCBI] 0.000164145
EFNB1 [NCBI] 0.000161891
oculopalatoskeletal syndrome [NCBI] 0.000150194
cutis gyrata syndrome of beare and stevenson [NCBI] 0.000140629
ruvalcaba syndrome [NCBI] 0.000127369
SNAI1 [NCBI] 0.000107822
LDS [NCBI] 0.000105019
craniosynostosis with anomalies of the cranial base and digits [NCBI] 9.74931e-05
craniosynostosis with ocular abnormalities and hallucal defects [NCBI] 9.74931e-05
craniosynostosis, calcification of basal ganglia, and facial dysmorphism [NCBI] 9.74931e-05
aurocephalosyndactyly [NCBI] 9.74931e-05
craniosynostosis [NCBI] 9.74931e-05
craniosynostosis-mental retardation-clefting syndrome [NCBI] 9.74931e-05
scaphocephaly, maxillary retrusion, and mental retardation [NCBI] 9.74931e-05
craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus [NCBI] 9.74931e-05
lambdoid synostosis [NCBI] 9.74931e-05
craniosynostosis, philadelphia type [NCBI] 9.74931e-05
spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation [NCBI] 9.74931e-05
craniosynostosis syndrome, autosomal recessive [NCBI] 9.74931e-05
holoprosencephaly, semilobar, with craniosynostosis [NCBI] 9.74931e-05
acrocephalopolysyndactyly type iii [NCBI] 9.74931e-05
acrocraniofacial dysostosis [NCBI] 9.74931e-05
JBS [NCBI] 9.20892e-05
frontoocular syndrome [NCBI] 7.506e-05
summitt syndrome [NCBI] 7.506e-05
craniorhiny [NCBI] 7.506e-05
holoprosencephaly, ectrodactyly, and bilateral cleft lip/palate [NCBI] 7.506e-05
craniosynostosis-microcephaly with chromosomal breakage and other abnormalities [NCBI] 7.506e-05
MCOP3 [NCBI] 6.66174e-05
acrocephalopolydactylous dysplasia [NCBI] 6.66174e-05
craniofacial dyssynostosis with short stature [NCBI] 6.66174e-05
MCOPS5 [NCBI] 6.66174e-05
craniotelencephalic dysplasia [NCBI] 6.66174e-05
carnevale syndrome [NCBI] 6.66174e-05
GCPS [NCBI] 6.41212e-05
microcephaly with chemotactic defect and transient hypogammaglobulinemia [NCBI] 6.11486e-05
P4HA3 [NCBI] 5.9054e-05
TWISTNB [NCBI] 5.9054e-05
apnea, obstructive sleep [NCBI] 5.83437e-05
MCOP2 [NCBI] 5.70922e-05
robinow-sorauf syndrome [NCBI] 5.70922e-05
mental retardation, fra12a type [NCBI] 5.38677e-05
cerebellotrigeminal dermal dysplasia [NCBI] 5.38677e-05
SOX6 [NCBI] 5.3859e-05
TD2 [NCBI] 4.89087e-05
frontonasal dysplasia [NCBI] 4.89087e-05
MFS2 [NCBI] 4.69167e-05
OGD [NCBI] 4.69167e-05
lenz-majewski hyperostotic dwarfism [NCBI] 4.51513e-05
cherubism [NCBI] 4.51513e-05
MCOPS9 [NCBI] 4.35672e-05
sc phocomelia syndrome [NCBI] 4.35672e-05
wildervanck syndrome [NCBI] 4.2131e-05
RECQL4 [NCBI] 4.16715e-05
MCOPS2 [NCBI] 3.96095e-05
TCF3 [NCBI] 3.9582e-05
MFS [NCBI] 3.86604e-05
BDC [NCBI] 3.84902e-05
PFM [NCBI] 3.84902e-05
MCOPS3 [NCBI] 3.6474e-05
FMD [NCBI] 3.55595e-05
GLDC [NCBI] 3.40012e-05
NOG [NCBI] 3.29935e-05
hyperimmunoglobulin e recurrent infection syndrome, autosomal dominant [NCBI] 2.9188e-05
FGF8 [NCBI] 2.81955e-05
MCOPS7 [NCBI] 2.61167e-05
HCH [NCBI] 2.52277e-05
FGF2 [NCBI] 2.40376e-05
FDH [NCBI] 2.14974e-05
IHH [NCBI] 2.10395e-05
RTS [NCBI] 1.8352e-05
sotos syndrome [NCBI] 1.8352e-05
FBN1 [NCBI] 1.70012e-05
TCOF [NCBI] 1.58563e-05
ALGS1 [NCBI] 1.52599e-05
TD1 [NCBI] 1.36423e-05
EGF [NCBI] 8.00426e-06
SHH [NCBI] 7.42315e-06
ACP5 [NCBI] 6.18531e-06
DGS [NCBI] 4.13733e-06
CPI [NCBI] 3.19539e-06
FA [NCBI] 1.7638e-06
AVP [NCBI] 1.12288e-07



Database Center for Life Science