Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Coccyx [NCBI]


Gene


Gene Link Information
Gain
01
MNX1 [NCBI] 2.78282e-05
FGFR2 [NCBI] 6.5202e-06
ACP5 [NCBI] 4.83814e-06




OMIM


OMIM Link Information
gain
01
schinzel-giedion midface-retraction syndrome [NCBI] 0.00135232
sacral defect with anterior meningocele [NCBI] 0.000361749
chondrodysplasia punctata, brachytelephalangic, autosomal [NCBI] 0.000264513
teebi-shaltout syndrome [NCBI] 0.000225238
cerebrocostomandibular syndrome [NCBI] 0.000162475
ACP5 [NCBI] 3.19515e-05
TNFRSF11B [NCBI] 3.06922e-05
CEACAM5 [NCBI] 2.37161e-05




Database Center for Life Science