Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Maxillofacial Development	[NCBI]

Gene	Link	Information Gain
HFM	[NCBI]	0.000616178
SHH	[NCBI]	7.79968e-06
CNOT3	[NCBI]	3.98697e-06
TRH	[NCBI]	3.7261e-06
GAK	[NCBI]	3.5862e-06
SH3GL1	[NCBI]	3.50509e-06
EIF2B1	[NCBI]	3.48689e-06
TRIP10	[NCBI]	3.42059e-06
AP1B1	[NCBI]	3.34936e-06
FOXJ1	[NCBI]	3.31142e-06
ZBTB17	[NCBI]	3.09384e-06
EGFR	[NCBI]	2.8944e-06
GLI3	[NCBI]	2.63079e-06
TWIST1	[NCBI]	2.58685e-06
MSTN	[NCBI]	2.49566e-06
FGFR1	[NCBI]	2.46452e-06
DLX3	[NCBI]	2.45154e-06
FGFR2	[NCBI]	2.41469e-06
SOX9	[NCBI]	2.30057e-06
EGF	[NCBI]	2.20964e-06
MMP2	[NCBI]	2.14286e-06
BMP7	[NCBI]	2.1328e-06
FGFR3	[NCBI]	2.07118e-06
NOG	[NCBI]	2.04215e-06
CREBBP	[NCBI]	1.91697e-06
PAX6	[NCBI]	1.83895e-06
ACP5	[NCBI]	1.82412e-06
BMP2	[NCBI]	1.66404e-06
VIP	[NCBI]	1.39194e-06

OMIM	Link	Information gain
HFM	[NCBI]	0.00316582
prognathism, mandibular	[NCBI]	0.00081137
molar i reinclusion	[NCBI]	0.00076331
maxillonasal dysplasia, binder type	[NCBI]	0.000693313
holoprosencephaly	[NCBI]	0.000416511
kabuki syndrome	[NCBI]	0.000392504
CCD	[NCBI]	0.000245738
HPE3	[NCBI]	0.000212253
CPI	[NCBI]	0.000188229
metaphyseal dysplasia with maxillary hypoplasia and brachydactyly	[NCBI]	0.00016457
brachioskeletogenital syndrome	[NCBI]	0.00016457
amelogenesis imperfecta, hypoplastic, and openbite malocclusion, autosomal recessive	[NCBI]	0.000126323
progeroid short stature with pigmented nevi	[NCBI]	0.000126323
OGD	[NCBI]	0.000126323
AIH2	[NCBI]	0.000104219
FMD	[NCBI]	9.94879e-05
BWS	[NCBI]	9.44959e-05
mannosidosis, alpha b, lysosomal	[NCBI]	8.31804e-05
fragile x mental retardation syndrome	[NCBI]	4.37599e-05
MSTN	[NCBI]	3.05076e-05
apnea, obstructive sleep	[NCBI]	2.69777e-05
RBP1	[NCBI]	2.56015e-05
FGFR1	[NCBI]	2.46563e-05
FGFR2	[NCBI]	2.34382e-05
EGFR	[NCBI]	1.80315e-05
GNRH1	[NCBI]	1.39582e-05
SHH	[NCBI]	1.31659e-05
EGF	[NCBI]	9.00015e-06
VIP	[NCBI]	7.36773e-06
CEACAM5	[NCBI]	7.17368e-06
CF	[NCBI]	2.51261e-06