Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Odontodysplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
GJA1 [NCBI] 0.000100987
WNT10A [NCBI] 1.54543e-05
WNT6 [NCBI] 1.51086e-05
VIL1 [NCBI] 1.51086e-05
DNAJB2 [NCBI] 1.48211e-05
EPHA4 [NCBI] 1.3697e-05
INHA [NCBI] 1.11688e-05
CDKN1A [NCBI] 4.0957e-06



OMIM


 OMIM Link Information
gain		 01
singleton-merten syndrome [NCBI] 0.00107364
amelogenesis imperfecta, hypoplastic type [NCBI] 0.000991404
dentin dysplasia, type i [NCBI] 0.000898321
ODDD [NCBI] 0.000538959
OODD [NCBI] 0.000257207
deafness, autosomal recessive [NCBI] 0.000127588
GJA1 [NCBI] 0.000115574
WNT10A [NCBI] 0.000109108
syndactyly, type iii [NCBI] 0.000106243
AIH2 [NCBI] 9.9178e-05
dentinogenesis imperfecta, shields type iii [NCBI] 9.73745e-05
DGI1 [NCBI] 8.94427e-05



Database Center for Life Science