Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Maxillofacial Abnormalities [NCBI]


Gene


Gene Link Information
Gain
01
UBR2 [NCBI] 1.56695e-05
UBR1 [NCBI] 1.378e-05
COL11A1 [NCBI] 1.378e-05
ZEB2 [NCBI] 1.13839e-05
FGF8 [NCBI] 1.09179e-05
FOXC1 [NCBI] 1.08941e-05
COL11A2 [NCBI] 1.03509e-05
EDA [NCBI] 1.03167e-05
COL2A1 [NCBI] 9.57397e-06
FGFR2 [NCBI] 9.21896e-06
BMP4 [NCBI] 8.94015e-06
PAX6 [NCBI] 8.46147e-06




OMIM


OMIM Link Information
gain
01
kabuki syndrome [NCBI] 0.000510457
klippel-trenaunay-weber syndrome [NCBI] 0.000459121
van buchem disease, type 2 [NCBI] 0.000134657
adenylosuccinase deficiency [NCBI] 0.000108274
UBR1 [NCBI] 9.5327e-05
JBS [NCBI] 8.97638e-05
DA2A [NCBI] 8.3549e-05
SJS1 [NCBI] 7.90724e-05
apnea, obstructive sleep [NCBI] 7.89651e-05
FGFR2 [NCBI] 5.04603e-05
AS [NCBI] 4.72365e-05
AVP [NCBI] 2.51854e-05




Database Center for Life Science