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MeSH keywords -> Related genes, diseases (OMIM)


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01 Meningocele [NCBI]


Gene


Gene Link Information
Gain
01
MNX1 [NCBI] 9.63982e-05
MAP7 [NCBI] 1.58882e-05
NCAM1 [NCBI] 1.12006e-05
GLI3 [NCBI] 1.04162e-05




OMIM


OMIM Link Information
gain
01
lateral meningocele syndrome [NCBI] 0.00213636
sacral defect with anterior meningocele [NCBI] 0.000903751
mohr syndrome [NCBI] 0.000725612
currarino syndrome [NCBI] 0.000535282
HLXB9 [NCBI] 0.000181387
cholesterol pneumonia [NCBI] 0.000135008
reese retinal dysplasia [NCBI] 0.000135008
MKS1 [NCBI] 0.000128854
sakoda complex [NCBI] 0.000104061
aminopterin syndrome sine aminopterin [NCBI] 9.85565e-05
MFS [NCBI] 8.26103e-05
WZS [NCBI] 7.79043e-05
mulibrey nanism [NCBI] 7.24669e-05
ARX [NCBI] 6.24949e-05
velocardiofacial syndrome [NCBI] 5.03074e-05
NF1 [NCBI] 3.83453e-05
DGS [NCBI] 3.51753e-05




Database Center for Life Science