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MeSH keywords -> Related genes, diseases (OMIM)


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01 Dental Enamel Hypoplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
ENAM [NCBI] 2.74373e-05
DLX3 [NCBI] 2.29958e-05
LAMB3 [NCBI] 1.59751e-05
AMELX [NCBI] 1.19012e-05
COL17A1 [NCBI] 1.06467e-05
AXIN2 [NCBI] 1.0524e-05
TGFB1 [NCBI] 1.03458e-05
EDA [NCBI] 9.07083e-06
FGFR1 [NCBI] 8.80544e-06
TRPV1 [NCBI] 8.7071e-06
NF1 [NCBI] 8.48948e-06
CFTR [NCBI] 3.29306e-06



OMIM


 OMIM Link Information
gain		 01
amelogenesis imperfecta, hypoplastic type [NCBI] 0.003153
kohlschutter-tonz syndrome [NCBI] 0.00232174
oculodentoosseous dysplasia, recessive [NCBI] 0.00165256
ameloonychohypohidrotic syndrome [NCBI] 0.0010375
singleton-merten syndrome [NCBI] 0.000819746
ODDD [NCBI] 0.000667141
cenani syndactylism [NCBI] 0.000644945
oculocerebral syndrome with hypopigmentation [NCBI] 0.00056504
trichodentoosseous syndrome [NCBI] 0.000440632
amelogenesis imperfecta, hypoplastic, and openbite malocclusion, autosomal recessive [NCBI] 0.000211065
TS [NCBI] 0.000201644
AIH2 [NCBI] 0.000164793
lenz-majewski hyperostotic dwarfism [NCBI] 0.000160965
SRS [NCBI] 0.000147464
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 0.000146647
enamel hypoplasia, cataracts, and aqueductal stenosis [NCBI] 0.000120847
trichoodontoonychial dysplasia [NCBI] 0.000120847
pfeiffer-palm-teller syndrome [NCBI] 0.000120847
neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia [NCBI] 0.000120847
AI1G [NCBI] 8.99103e-05
alaninuria with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus [NCBI] 8.99103e-05
GJA1 [NCBI] 8.98935e-05
hearing loss, sensorineural, with enamel hypoplasia and nail defects [NCBI] 8.44113e-05
AIHHT [NCBI] 7.70698e-05
syndactyly, type iii [NCBI] 7.70698e-05
dentinogenesis imperfecta, shields type iii [NCBI] 6.82323e-05
ENAM [NCBI] 6.48204e-05
LADD [NCBI] 6.38082e-05
AMELX [NCBI] 6.23221e-05
seckel syndrome 1 [NCBI] 5.83982e-05
CIPA [NCBI] 5.66621e-05
PITX2 [NCBI] 5.60041e-05
HSS [NCBI] 5.36741e-05
RIEG1 [NCBI] 5.11628e-05
epidermolysis bullosa letalis [NCBI] 5.05931e-05
mucopolysaccharidosis type iva [NCBI] 4.8838e-05
FGFR1 [NCBI] 4.40056e-05
costello syndrome [NCBI] 4.06158e-05
RTS [NCBI] 4.00394e-05
SLS [NCBI] 3.42435e-05
SVAS [NCBI] 3.38643e-05
APS1 [NCBI] 3.03834e-05
CD [NCBI] 2.71671e-05
CFTR [NCBI] 1.90616e-05
CF [NCBI] 8.22569e-06
PWS [NCBI] 5.2256e-06



Database Center for Life Science