Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Sacrococcygeal Region [NCBI]

Gene


 Gene Link Information
Gain		 01
VUR [NCBI] 0.000244372
AFP [NCBI] 6.37912e-05
SHH [NCBI] 8.73198e-06
GFAP [NCBI] 8.55823e-06
MNX1 [NCBI] 6.02203e-06
LTB [NCBI] 5.62751e-06
NANOG [NCBI] 5.21969e-06
MADCAM1 [NCBI] 5.01562e-06
FGFR2 [NCBI] 4.67282e-06
POU5F1 [NCBI] 4.34214e-06
NOS1 [NCBI] 3.73861e-06
BMP7 [NCBI] 3.63973e-06
OPRL1 [NCBI] 3.61601e-06
MLH1 [NCBI] 3.60629e-06
ACP5 [NCBI] 3.00357e-06
PCNA [NCBI] 1.98025e-06
ACHE [NCBI] 1.72684e-06
NGF [NCBI] 1.25552e-06



OMIM


 OMIM Link Information
gain		 01
CHDM [NCBI] 0.00145218
schinzel-giedion midface-retraction syndrome [NCBI] 0.00104185
sacral defect with anterior meningocele [NCBI] 0.000329655
AFP [NCBI] 0.000323089
craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation [NCBI] 0.000250002
HPE3 [NCBI] 0.000152523
currarino syndrome [NCBI] 0.000147986
pfeiffer syndrome [NCBI] 0.00014231
sotos syndrome [NCBI] 0.000120673
TS [NCBI] 6.32595e-05
CEACAM5 [NCBI] 6.06478e-05
MUC1 [NCBI] 4.01485e-05
SLC17A7 [NCBI] 3.37979e-05
GFAP [NCBI] 2.73716e-05
PCNA [NCBI] 3.91179e-06
ACHE [NCBI] 2.50101e-06
NGFB [NCBI] 5.99888e-07



Database Center for Life Science