Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Occipital Bone [NCBI]

Gene


 Gene Link Information
Gain		 01
FND [NCBI] 0.00037067
AIS [NCBI] 0.000211065
ATP7A [NCBI] 2.21166e-05
PAX1 [NCBI] 1.42308e-05
COL18A1 [NCBI] 6.99905e-06
TWIST1 [NCBI] 6.07681e-06
VIM [NCBI] 5.73922e-06
PAM [NCBI] 5.27701e-06
NOG [NCBI] 4.66803e-06
GFAP [NCBI] 2.92657e-06



OMIM


 OMIM Link Information
gain		 01
chiari malformation type i [NCBI] 0.00191012
varadi-papp syndrome [NCBI] 0.000840987
DWS [NCBI] 0.000700868
cutis laxa, x-linked [NCBI] 0.000601238
KNO [NCBI] 0.000494389
IS1 [NCBI] 0.000351307
menkes disease [NCBI] 0.000306526
cephalocele, atretic [NCBI] 0.000217625
hair whorl [NCBI] 0.000153933
crouzon syndrome [NCBI] 0.000128777
hydrolethalus syndrome 1 [NCBI] 0.000125636
RA [NCBI] 0.000116629
apert syndrome [NCBI] 0.000113711
FHM1 [NCBI] 0.000111834
ATP7A [NCBI] 0.000102561
SCDO1 [NCBI] 9.02246e-05
MDLS [NCBI] 8.78329e-05
MKS1 [NCBI] 8.05101e-05
MNT [NCBI] 5.94505e-05
COL18A1 [NCBI] 5.02619e-05
VIM [NCBI] 3.50531e-05
PAM [NCBI] 3.43277e-05
MUC1 [NCBI] 2.4651e-05
GFAP [NCBI] 1.05251e-05



Database Center for Life Science