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MeSH keywords -> Related genes, diseases (OMIM)


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01 Mandibulofacial Dysostosis [NCBI]


Gene


Gene Link Information
Gain
01
HFM [NCBI] 0.000779153
TCOF1 [NCBI] 0.00069886
FND [NCBI] 0.000282619
HS3ST5 [NCBI] 3.42088e-05
RBM22 [NCBI] 1.66899e-05
NOL5A [NCBI] 1.43094e-05
PRRX2 [NCBI] 1.3411e-05
NDST1 [NCBI] 1.23939e-05
EVC2 [NCBI] 1.17608e-05
NOLC1 [NCBI] 1.15147e-05
TBL1X [NCBI] 1.12996e-05
TNIP1 [NCBI] 1.05051e-05
EVC [NCBI] 1.0268e-05
OFD1 [NCBI] 1.01607e-05
CSNK2A2 [NCBI] 1.00598e-05
PRRX1 [NCBI] 9.96442e-06
MYOT [NCBI] 8.84682e-06
CDX1 [NCBI] 8.20955e-06
YY1 [NCBI] 8.14433e-06
PITX1 [NCBI] 7.93389e-06
RPS19 [NCBI] 7.55508e-06
PAFAH1B1 [NCBI] 7.04958e-06
SOX9 [NCBI] 6.45925e-06
FHIT [NCBI] 4.22567e-06




OMIM


OMIM Link Information
gain
01
HFM [NCBI] 0.00864602
TCOF [NCBI] 0.00672212
POADS [NCBI] 0.00424368
maxillofacial dysostosis [NCBI] 0.00185702
TCOF1 [NCBI] 0.00184408
acrodysostosis [NCBI] 0.00111036
AFD1 [NCBI] 0.000640114
hemifacial microsomia with radial defects [NCBI] 0.000533713
lateral meningocele syndrome [NCBI] 0.000533713
branchial arch syndrome, x-linked [NCBI] 0.000439076
acrofacial dysostosis syndrome of rodriguez [NCBI] 0.000361638
mandibulofacial dysostosis, treacher collins type, autosomal recessive [NCBI] 0.000329068
MNS [NCBI] 0.000267154
HSS [NCBI] 0.000264147
acrofacial dysostosis, catania type [NCBI] 0.00021922
NDST1 [NCBI] 0.000208113
cataract, membranous [NCBI] 0.000109532
mandibulofacial dysostosis syndrome, bauru type [NCBI] 0.000109532
growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate [NCBI] 0.000109532
mandibulofacial dysostosis with ptosis, autosomal dominant [NCBI] 0.000109532
mandibulofacial dysostosis with macroblepharon and macrostomia [NCBI] 0.000109532
lambert syndrome [NCBI] 8.70777e-05
split-foot deformity with mandibulofacial dysostosis [NCBI] 7.86143e-05
WS1 [NCBI] 7.76269e-05
robin sequence with cleft mandible and limb anomalies [NCBI] 7.31247e-05
PRRX2 [NCBI] 7.10704e-05
CDX1 [NCBI] 7.10704e-05
TBL1X [NCBI] 6.58708e-05
weyers acrofacial dysostosis [NCBI] 6.58022e-05
aglossia-adactylia [NCBI] 6.58022e-05
PITX1 [NCBI] 6.24949e-05
PMX1 [NCBI] 5.99851e-05
serpentine fibula-polycystic kidney syndrome [NCBI] 5.87887e-05
EVC2 [NCBI] 5.63228e-05
DBA [NCBI] 5.60192e-05
frank-ter haar syndrome [NCBI] 5.48997e-05
CXORF5 [NCBI] 5.25509e-05
PDGFRB [NCBI] 4.90631e-05
UBTF [NCBI] 4.90631e-05
FMD [NCBI] 4.72443e-05
pycnodysostosis [NCBI] 4.72443e-05
crouzon syndrome [NCBI] 4.55272e-05
PAFAH1B1 [NCBI] 4.49227e-05
MADA [NCBI] 4.12904e-05
diastrophic dysplasia [NCBI] 4.12904e-05
OFD1 [NCBI] 4.01038e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 3.95435e-05
ODDD [NCBI] 3.61144e-05
PAX3 [NCBI] 3.42405e-05
HGPS [NCBI] 2.46328e-05
GJA1 [NCBI] 2.43228e-05
CD [NCBI] 1.83717e-05
BCNS [NCBI] 1.32133e-05




Database Center for Life Science