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01 Jaw Abnormalities [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.000291504
ANO5 [NCBI] 1.72206e-05
NAV2 [NCBI] 1.58575e-05
SLC6A5 [NCBI] 1.58575e-05
SLC17A6 [NCBI] 1.53238e-05
GAS2 [NCBI] 1.53238e-05
NELL1 [NCBI] 1.49174e-05
HTATIP2 [NCBI] 1.34363e-05
SOST [NCBI] 1.30917e-05
TRPS1 [NCBI] 1.30917e-05
FANCF [NCBI] 1.24271e-05
NAT1 [NCBI] 9.70788e-06
NAT2 [NCBI] 8.1628e-06
VDR [NCBI] 6.94365e-06
AFP [NCBI] 5.44994e-06



OMIM


 OMIM Link Information
gain		 01
dysgnathia complex [NCBI] 0.00258477
HFH [NCBI] 0.000807657
molar i reinclusion [NCBI] 0.000632907
auriculocondylar syndrome [NCBI] 0.000632907
HFM [NCBI] 0.000608544
STHAG4 [NCBI] 0.000575369
GO [NCBI] 0.000533572
AMCN [NCBI] 0.000461898
ACC [NCBI] 0.000431005
marden-walker syndrome [NCBI] 0.000421975
OFC1 [NCBI] 0.000254316
PPS [NCBI] 0.000250088
MSX1 [NCBI] 0.00022524
GDD [NCBI] 0.000192232
multiple epiphyseal dysplasia with robin phenotype [NCBI] 0.000132242
CCD [NCBI] 0.000111895
arthrogryposis, distal, type 2e [NCBI] 0.000109774
brachyphalangy, polydactyly, and tibial aplasia/hypoplasia [NCBI] 9.57923e-05
robin sequence with cleft mandible and limb anomalies [NCBI] 9.57923e-05
acrorenal-mandibular syndrome [NCBI] 9.17009e-05
aglossia-adactylia [NCBI] 8.84414e-05
TMEM16E [NCBI] 8.05705e-05
cherubism [NCBI] 7.95849e-05
ankyloblepharon-ectodermal defects-cleft lip/palate [NCBI] 7.79657e-05
DA2B [NCBI] 7.3903e-05
cerebrocostomandibular syndrome [NCBI] 7.27487e-05
GSC [NCBI] 7.26806e-05
FMD [NCBI] 6.97129e-05
SOST [NCBI] 6.79674e-05
VWS [NCBI] 4.95373e-05
AMC [NCBI] 4.78217e-05
CD [NCBI] 3.94317e-05
BCNS [NCBI] 3.35043e-05
WBS [NCBI] 3.11672e-05
SLOS [NCBI] 2.95637e-05
VDR [NCBI] 2.36545e-05
apnea, obstructive sleep [NCBI] 2.27475e-05
AFP [NCBI] 1.34902e-05
APC [NCBI] 6.92922e-06



Database Center for Life Science