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MeSH keywords -> Related genes, diseases (OMIM)


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01 Tooth Discoloration [NCBI]

Gene


 Gene Link Information
Gain		 01
COL1A1 [NCBI] 1.4128e-05



OMIM


 OMIM Link Information
gain		 01
ameloonychohypohidrotic syndrome [NCBI] 0.00129156
amelogenesis imperfecta, hypoplastic type [NCBI] 0.000991404
cholestasis-lymphedema syndrome [NCBI] 0.000866698
erythema of acral regions [NCBI] 0.000154415
sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth [NCBI] 0.000154415
dentin dysplasia, type ii [NCBI] 0.000105561
AIH2 [NCBI] 0.00010353
dentinogenesis imperfecta, shields type iii [NCBI] 0.000101727
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus [NCBI] 0.000100104
DGI1 [NCBI] 9.37927e-05
periodontitis, aggressive, 1 [NCBI] 8.84935e-05
NFE2L2 [NCBI] 8.57716e-05
ODDD [NCBI] 8.03786e-05
mucopolysaccharidosis type iva [NCBI] 6.49988e-05
CF [NCBI] 3.44722e-06



Database Center for Life Science