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MeSH keywords -> Related genes, diseases (OMIM)


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01 Dentinogenesis Imperfecta [NCBI]


Gene


Gene Link Information
Gain
01
DSPP [NCBI] 0.000364715
DMP1 [NCBI] 0.000111272
MEPE [NCBI] 3.62992e-05
IBSP [NCBI] 2.59593e-05
COL1A2 [NCBI] 8.01505e-06
TGFB1 [NCBI] 7.91829e-06
SPP1 [NCBI] 6.92058e-06
COL1A1 [NCBI] 6.50085e-06




OMIM


OMIM Link Information
gain
01
dentin dysplasia, type i [NCBI] 0.00213636
DGI1 [NCBI] 0.00180205
DSPP [NCBI] 0.00111216
dentinogenesis imperfecta, shields type iii [NCBI] 0.000985278
ehlers-danlos syndrome, type vib [NCBI] 0.000765046
dentin dysplasia, type ii [NCBI] 0.000437894
periodontitis, aggressive, 1 [NCBI] 0.000252914
spondylometaphyseal dysplasia with dentinogenesis imperfecta [NCBI] 0.000231686
osteogenesis imperfecta, type i [NCBI] 0.000184861
IBSP [NCBI] 0.000156795
DMP1 [NCBI] 0.000142329
deafness, autosomal dominant 39, with dentinogenesis imperfecta 1 [NCBI] 0.000131018
osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones, but without fractures [NCBI] 0.000131018
GC [NCBI] 0.000100207
AIHHT [NCBI] 8.72191e-05
trichodentoosseous syndrome [NCBI] 6.94441e-05
SMPD3 [NCBI] 6.86721e-05
osteogenesis imperfecta, type iv [NCBI] 6.67501e-05
osteogenesis imperfecta, type iii [NCBI] 6.44447e-05
DSP [NCBI] 4.98678e-05
osteogenesis imperfecta, type iia [NCBI] 4.88614e-05
SPP1 [NCBI] 4.28786e-05
COL1A2 [NCBI] 3.44507e-05




Database Center for Life Science