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01 Mouth Abnormalities [NCBI]

Gene


 Gene Link Information
Gain		 01
VCF [NCBI] 0.000401057
TP63 [NCBI] 3.66084e-05
CKAP4 [NCBI] 2.79854e-05
IRF6 [NCBI] 2.20082e-05
SCN3B [NCBI] 1.87183e-05
OSR2 [NCBI] 1.63379e-05
C6orf105 [NCBI] 1.63379e-05
IMP5 [NCBI] 1.63379e-05
SFRS15 [NCBI] 1.54394e-05
BHMT2 [NCBI] 1.48559e-05
B3GALTL [NCBI] 1.44221e-05
HNRNPAB [NCBI] 1.40763e-05
ZNF202 [NCBI] 1.37888e-05
OSR1 [NCBI] 1.35427e-05
RPLP0 [NCBI] 1.31364e-05
MLPH [NCBI] 1.26649e-05
OFD1 [NCBI] 1.21881e-05
ALX4 [NCBI] 1.19012e-05
GNB2L1 [NCBI] 1.11906e-05
HDAC4 [NCBI] 1.11906e-05
BHMT [NCBI] 1.10243e-05
CRHR1 [NCBI] 1.08728e-05
ACTB [NCBI] 1.08251e-05
SP100 [NCBI] 1.06048e-05
LEF1 [NCBI] 1.00453e-05
ADH1C [NCBI] 9.05403e-06
APEX1 [NCBI] 9.03738e-06
KRT14 [NCBI] 8.39593e-06
EPHX1 [NCBI] 8.29647e-06
OGG1 [NCBI] 8.26456e-06
XRCC3 [NCBI] 8.26456e-06
FGFR2 [NCBI] 7.97456e-06
CD44 [NCBI] 7.48364e-06
GAPDH [NCBI] 6.95037e-06
HNF1B [NCBI] 6.9262e-06
XRCC1 [NCBI] 6.90237e-06
ERCC2 [NCBI] 6.76166e-06
CYP1A1 [NCBI] 6.67672e-06
MAPT [NCBI] 6.12357e-06
MTHFR [NCBI] 4.70883e-06
VWF [NCBI] 3.8571e-06



OMIM


 OMIM Link Information
gain		 01
OFD4 [NCBI] 0.00111016
varadi-papp syndrome [NCBI] 0.00100541
coffin-siris syndrome [NCBI] 0.000814478
cleft palate-lateral synechia syndrome [NCBI] 0.000742078
OFD8 [NCBI] 0.000660154
branchiootic syndrome 2 [NCBI] 0.000660154
torus palatinus and torus mandibularis [NCBI] 0.000660154
hypertelorism with esophageal abnormality and hypospadias [NCBI] 0.000610749
blepharocheilodontic syndrome [NCBI] 0.000488197
HFM [NCBI] 0.000482319
facial ectodermal dysplasia [NCBI] 0.000397762
AMCN [NCBI] 0.000397762
OFD1 [NCBI] 0.000389934
robinow syndrome, autosomal dominant [NCBI] 0.000349925
PPS [NCBI] 0.00030355
EEC1 [NCBI] 0.000257436
ATD1 [NCBI] 0.000253288
OPD2 [NCBI] 0.000232404
OFC1 [NCBI] 0.000195005
crumpled helices and small mouth [NCBI] 0.000119929
DA2A [NCBI] 0.000116203
B3GALTL [NCBI] 0.000101216
VWS [NCBI] 9.75105e-05
RSTS [NCBI] 9.75105e-05
arthrogryposis, distal, type 2e [NCBI] 9.74659e-05
temtamy preaxial brachydactyly syndrome [NCBI] 9.74659e-05
velocardiofacial syndrome [NCBI] 9.35922e-05
SRS [NCBI] 8.68047e-05
oroacral syndrome, verloes-koulischer type [NCBI] 8.34951e-05
brachycephaly, deafness, cataract, microstomia, and mental retardation [NCBI] 8.34951e-05
hunter-mcalpine craniosynostosis syndrome [NCBI] 7.9409e-05
holzgreve syndrome [NCBI] 7.9409e-05
malpuech facial clefting syndrome [NCBI] 7.9409e-05
cleft lip/palate with abnormal thumbs and microcephaly [NCBI] 7.61547e-05
cleft, median, of upper lip with polyps of facial skin and nasal mucosa [NCBI] 7.61547e-05
MYH8 [NCBI] 7.43448e-05
LGR8 [NCBI] 7.43448e-05
rokitansky-kuster-hauser syndrome [NCBI] 7.11362e-05
peters-plus syndrome [NCBI] 6.91144e-05
whistling face syndrome, recessive form [NCBI] 6.91144e-05
CXORF5 [NCBI] 6.8904e-05
BHMT [NCBI] 6.79086e-05
floating-harbor syndrome [NCBI] 6.73194e-05
lenz-majewski hyperostotic dwarfism [NCBI] 6.73194e-05
trismus-pseudocamptodactyly syndrome [NCBI] 6.73194e-05
char syndrome [NCBI] 6.73194e-05
IRF6 [NCBI] 6.34153e-05
PFM [NCBI] 6.05095e-05
LRS1 [NCBI] 5.94379e-05
pitt syndrome [NCBI] 5.94379e-05
seckel syndrome 1 [NCBI] 5.74896e-05
FMD [NCBI] 5.74896e-05
weaver syndrome [NCBI] 5.27688e-05
OKS [NCBI] 4.91413e-05
PKS [NCBI] 4.76007e-05
EVC [NCBI] 4.49132e-05
BRCA2 [NCBI] 4.34411e-05
COH1 [NCBI] 4.33501e-05
FDH [NCBI] 4.26243e-05
ED1 [NCBI] 3.97269e-05
MKS1 [NCBI] 3.80629e-05
WHS [NCBI] 3.15697e-05
CD [NCBI] 2.7732e-05
CDLS1 [NCBI] 2.7732e-05
DBA [NCBI] 2.71e-05
DGS [NCBI] 2.11853e-05
CPI [NCBI] 1.96176e-05
SLOS [NCBI] 1.84147e-05
polycystic kidneys [NCBI] 1.10522e-05
CEACAM5 [NCBI] 1.00944e-05



Database Center for Life Science