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01 Tooth Abnormalities [NCBI]


Gene


Gene Link Information
Gain
01
HYD2 [NCBI] 0.000438875
HFM [NCBI] 0.000230814
GJA1 [NCBI] 0.000136436
PITX2 [NCBI] 9.11103e-05
DLX3 [NCBI] 8.59481e-05
EDA [NCBI] 6.48971e-05
PAX9 [NCBI] 6.1177e-05
NHS [NCBI] 5.92815e-05
FOXC1 [NCBI] 4.62512e-05
TP63 [NCBI] 3.88922e-05
PITX1 [NCBI] 3.66576e-05
PITX3 [NCBI] 3.57855e-05
EVC [NCBI] 3.32174e-05
FGF3 [NCBI] 2.21543e-05
BCOR [NCBI] 2.20113e-05
DLX4 [NCBI] 1.85986e-05
IKBKE [NCBI] 1.77191e-05
CHUK [NCBI] 1.71977e-05
IKBKB [NCBI] 1.71668e-05
FGF10 [NCBI] 1.68475e-05
KCNJ2 [NCBI] 1.66264e-05
DPF3 [NCBI] 1.54743e-05
COL27A1 [NCBI] 1.54743e-05
IRF6 [NCBI] 1.54342e-05
MTRF1L [NCBI] 1.3094e-05
C6orf211 [NCBI] 1.3094e-05
RWDD1 [NCBI] 1.21957e-05
RSPO3 [NCBI] 1.21957e-05
UNQ1887 [NCBI] 1.21957e-05
NRXN3 [NCBI] 1.21957e-05
STK32B [NCBI] 1.21957e-05
AKAP2 [NCBI] 1.16124e-05
MTHFD1L [NCBI] 1.16124e-05
SASH1 [NCBI] 1.16124e-05
LHX8 [NCBI] 1.16124e-05
SNX3 [NCBI] 1.16124e-05
EPHB3 [NCBI] 1.16124e-05
PDSS2 [NCBI] 1.16124e-05
GIPC2 [NCBI] 1.11787e-05
WSB1 [NCBI] 1.11787e-05
PKN2 [NCBI] 1.11787e-05
PRUNE [NCBI] 1.11787e-05
SLC2A12 [NCBI] 1.08332e-05
SLC12A5 [NCBI] 1.08332e-05
BARX1 [NCBI] 1.08332e-05
CKAP4 [NCBI] 1.06053e-05
AUH [NCBI] 1.05458e-05
GABBR2 [NCBI] 1.05458e-05
EVC2 [NCBI] 1.05458e-05
FGF18 [NCBI] 1.02999e-05
OSR1 [NCBI] 1.02999e-05
TAAR6 [NCBI] 1.00849e-05
PTPN3 [NCBI] 1.00849e-05
TCF21 [NCBI] 9.89391e-06
GART [NCBI] 9.89391e-06
AGPAT2 [NCBI] 9.72211e-06
PRSS8 [NCBI] 9.72211e-06
TGFBR1 [NCBI] 9.61581e-06
ENPEP [NCBI] 9.566e-06
FBP1 [NCBI] 9.566e-06
SLC7A11 [NCBI] 9.566e-06
LAMA4 [NCBI] 9.42294e-06
OSTM1 [NCBI] 9.42294e-06
IKZF3 [NCBI] 9.42294e-06
AHCY [NCBI] 9.42294e-06
KRT3 [NCBI] 8.94684e-06
OFD1 [NCBI] 8.94684e-06
FZD7 [NCBI] 8.84598e-06
HSF2 [NCBI] 8.75074e-06
PRRX1 [NCBI] 8.75074e-06
PVRL1 [NCBI] 8.75074e-06
TGFBR3 [NCBI] 8.41538e-06
EDAR [NCBI] 8.26955e-06
ROR2 [NCBI] 8.26955e-06
HS3ST5 [NCBI] 8.20105e-06
TFAP2B [NCBI] 7.95164e-06
FOXE1 [NCBI] 7.95164e-06
SOX3 [NCBI] 7.8946e-06
GABRB3 [NCBI] 7.68381e-06
CA2 [NCBI] 7.58745e-06
ANKH [NCBI] 7.45243e-06
BSCL2 [NCBI] 7.32735e-06
AXIN2 [NCBI] 7.28762e-06
ST14 [NCBI] 7.2488e-06
MSX1 [NCBI] 7.2488e-06
SUMO1 [NCBI] 7.21084e-06
DSPP [NCBI] 7.13739e-06
GDF5 [NCBI] 6.93437e-06
GALNS [NCBI] 6.87177e-06
TGFA [NCBI] 6.81139e-06
CDH2 [NCBI] 6.58937e-06
INHBA [NCBI] 6.2174e-06
STAT5B [NCBI] 5.81164e-06
PDGFRA [NCBI] 5.77919e-06
FOXO3 [NCBI] 5.70072e-06
LIPC [NCBI] 5.67033e-06
FGFR1 [NCBI] 5.58236e-06
KRT5 [NCBI] 5.49879e-06
RUNX2 [NCBI] 5.47184e-06
POU1F1 [NCBI] 5.43222e-06
NOG [NCBI] 5.25886e-06
FYN [NCBI] 5.24715e-06
MTRR [NCBI] 5.14527e-06
TWIST1 [NCBI] 5.11266e-06
EPHX1 [NCBI] 5.08068e-06
TP73 [NCBI] 4.9883e-06
FGFR2 [NCBI] 4.76464e-06
EGF [NCBI] 4.72976e-06
IBSP [NCBI] 4.71319e-06
MITF [NCBI] 4.67151e-06
BMP4 [NCBI] 4.49244e-06
ADAM17 [NCBI] 4.26576e-06
NOTCH1 [NCBI] 4.14244e-06
BMP7 [NCBI] 4.13062e-06
ITGB3 [NCBI] 4.06143e-06
PAX6 [NCBI] 4.02794e-06
SHH [NCBI] 3.85533e-06
LAMB3 [NCBI] 3.57052e-06
FGFR3 [NCBI] 3.22727e-06
ERBB2 [NCBI] 3.06442e-06
TLR4 [NCBI] 1.96169e-06
STAT3 [NCBI] 1.81729e-06
HIF1A [NCBI] 1.39849e-06
PTH [NCBI] 3.55599e-07




OMIM


OMIM Link Information
gain
01
kbg syndrome [NCBI] 0.00397413
blepharocheilodontic syndrome [NCBI] 0.00314491
STHAG4 [NCBI] 0.00242527
RIEG2 [NCBI] 0.00202379
robinow syndrome, autosomal dominant [NCBI] 0.00165122
cranioectodermal dysplasia [NCBI] 0.00154932
mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth [NCBI] 0.00148175
oculodentoosseous dysplasia, recessive [NCBI] 0.00114777
ODDD [NCBI] 0.00106575
kabuki syndrome [NCBI] 0.00098122
EEC1 [NCBI] 0.000798777
STHAG2 [NCBI] 0.00078953
microcephalic osteodysplastic primordial dwarfism with tooth abnormalities [NCBI] 0.00078953
trichodentoosseous syndrome [NCBI] 0.00078592
NHS [NCBI] 0.000748016
microcephalic osteodysplastic primordial dwarfism, type ii [NCBI] 0.00074174
otodental dysplasia [NCBI] 0.000572601
teeth, odd shapes of [NCBI] 0.000572601
cerebrooculonasal syndrome [NCBI] 0.000572601
STHAG5 [NCBI] 0.000572601
HFH [NCBI] 0.000572601
PRS [NCBI] 0.000572601
IP [NCBI] 0.000513152
RIEG1 [NCBI] 0.000506533
axenfeld-rieger anomaly with cardiac defects and sensorineural hearing loss [NCBI] 0.000491365
cone-rod dystrophy and amelogenesis imperfecta [NCBI] 0.000491365
ED1 [NCBI] 0.000482155
weyers acrofacial dysostosis [NCBI] 0.000441477
anodontia of permanent dentition [NCBI] 0.000438973
LADD [NCBI] 0.000437362
HTC2 [NCBI] 0.000400278
molar i reinclusion [NCBI] 0.000400278
dentin dysplasia, type i [NCBI] 0.000400278
taurodontism [NCBI] 0.000388063
EVC [NCBI] 0.000383622
hypertrichosis universalis [NCBI] 0.000369652
maxillonasal dysplasia, binder type [NCBI] 0.000369652
HSS [NCBI] 0.000364473
syndactyly, type i, with microcephaly and mental retardation [NCBI] 0.000344358
HBD [NCBI] 0.000344358
GO [NCBI] 0.00030418
HTC1 [NCBI] 0.00030418
acrodysostosis [NCBI] 0.00030418
DA5 [NCBI] 0.000287707
MCOPS2 [NCBI] 0.000252691
mohr syndrome [NCBI] 0.000236553
DLX3 [NCBI] 0.000235768
AIHHT [NCBI] 0.000223642
JBS [NCBI] 0.00021358
dermoodontodysplasia [NCBI] 0.000193887
ectodermal dysplasia, trichoodontoonychial type [NCBI] 0.000193887
deafness, congenital, with inner ear agenesis, microtia, and microdontia [NCBI] 0.000193887
carabelli anomaly of maxillary molar teeth [NCBI] 0.000193887
NHS [NCBI] 0.000188263
adult syndrome [NCBI] 0.000177504
FDH [NCBI] 0.000170909
GJA1 [NCBI] 0.000170815
EEC3 [NCBI] 0.000163088
gorlin-chaudhry-moss syndrome [NCBI] 0.000162973
codas syndrome [NCBI] 0.000162973
SMMCI [NCBI] 0.000157251
MSX1 [NCBI] 0.000157068
RHS [NCBI] 0.000152058
OODD [NCBI] 0.000149023
oroacral syndrome, verloes-koulischer type [NCBI] 0.000149023
PITX2 [NCBI] 0.000143419
scalp-ear-nipple syndrome [NCBI] 0.00013946
CCD [NCBI] 0.00012987
ichthyosiform erythroderma, corneal involvement, and deafness [NCBI] 0.000126203
HMI [NCBI] 0.000125679
EVC [NCBI] 0.000123552
ALSG [NCBI] 0.000121206
dentinogenesis imperfecta, shields type iii [NCBI] 0.000113095
PAX9 [NCBI] 0.000107278
IRID2 [NCBI] 0.000106649
LMS [NCBI] 9.89357e-05
ectodermal dysplasia with natal teeth, turnpenny type [NCBI] 9.69075e-05
pilodental dysplasia with refractive errors [NCBI] 9.69075e-05
ectodermal dysplasia with adrenal cyst [NCBI] 9.69075e-05
odontomicronychial dysplasia [NCBI] 9.69075e-05
ectodermal dysplasia with mental retardation and syndactyly [NCBI] 9.69075e-05
dens in dente and palatal invaginations [NCBI] 9.69075e-05
teeth, noneruption of, with maxillary hypoplasia and genu valgum [NCBI] 9.69075e-05
teeth, congenital absence of, with taurodontia and sparse hair [NCBI] 9.69075e-05
spondyloepimetaphyseal dysplasia with abnormal dentition [NCBI] 9.69075e-05
dental noneruption [NCBI] 9.69075e-05
symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch [NCBI] 9.69075e-05
incisors, lower central, absence of [NCBI] 9.69075e-05
xanthinuria, type ii [NCBI] 9.69075e-05
ackerman syndrome [NCBI] 9.69075e-05
polydactyly, postaxial, with dental and vertebral anomalies [NCBI] 9.69075e-05
corneodermatoosseous syndrome [NCBI] 9.69075e-05
incisors, shovel-shaped [NCBI] 9.69075e-05
taurodontism, microdontia, and dens invaginatus [NCBI] 9.69075e-05
growth retardation, small and puffy hands and feet, and eczema [NCBI] 9.69075e-05
hypoplasia of teeth roots [NCBI] 9.69075e-05
STHAGX1 [NCBI] 9.69075e-05
FOXC1 [NCBI] 9.46333e-05
EDA [NCBI] 9.24269e-05
immunoosseous dysplasia, schimke type [NCBI] 9.09403e-05
OPTB3 [NCBI] 8.76029e-05
OFD1 [NCBI] 7.81531e-05
andersen cardiodysrhythmic periodic paralysis [NCBI] 7.70144e-05
aredyld [NCBI] 7.44759e-05
pallister w syndrome [NCBI] 7.44759e-05
temtamy preaxial brachydactyly syndrome [NCBI] 7.44759e-05
telecanthus [NCBI] 7.44759e-05
tooth size [NCBI] 7.44759e-05
deafness-oligodontia syndrome [NCBI] 7.44759e-05
tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities [NCBI] 7.44759e-05
tooth malformation [NCBI] 7.44759e-05
trichodental dysplasia [NCBI] 7.44759e-05
mucopolysaccharidosis type iva [NCBI] 7.25221e-05
PAX6 [NCBI] 7.03726e-05
neurofaciodigitorenal syndrome [NCBI] 6.60348e-05
steatocystoma multiplex with natal teeth [NCBI] 6.60348e-05
bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive facial features [NCBI] 6.60348e-05
CRMP1 [NCBI] 6.46273e-05
epidermolysis bullosa, late-onset localized junctional, with mental retardation [NCBI] 6.05675e-05
coloboma of macula with type b brachydactyly [NCBI] 6.05675e-05
robin sequence with cleft mandible and limb anomalies [NCBI] 6.05675e-05
DYNLL1 [NCBI] 5.94295e-05
splenogonadal fusion with limb defects and micrognathia [NCBI] 5.65125e-05
ED3 [NCBI] 5.65125e-05
BCOR [NCBI] 5.60554e-05
EYA2 [NCBI] 5.60554e-05
DKK1 [NCBI] 5.35473e-05
weyers ulnar ray/oligodactyly syndrome [NCBI] 5.32895e-05
STHAG1 [NCBI] 5.32895e-05
syndactyly, type iii [NCBI] 5.32895e-05
peters anomaly [NCBI] 5.32895e-05
witkop syndrome [NCBI] 5.32895e-05
RSTS [NCBI] 5.31124e-05
STHAG3 [NCBI] 5.06161e-05
anonychia congenita [NCBI] 5.06161e-05
EVC2 [NCBI] 4.98886e-05
dentin dysplasia, type ii [NCBI] 4.83334e-05
GALNT3 [NCBI] 4.72252e-05
FGF10 [NCBI] 4.72252e-05
SOX3 [NCBI] 4.72252e-05
FGF3 [NCBI] 4.61221e-05
MSX2 [NCBI] 4.513e-05
BDB1 [NCBI] 4.45789e-05
weill-marchesani syndrome, autosomal recessive [NCBI] 4.45789e-05
KCNJ2 [NCBI] 4.26414e-05
WHS [NCBI] 4.16876e-05
chromosome 18q deletion syndrome [NCBI] 4.15615e-05
SALL4 [NCBI] 4.12749e-05
ROR2 [NCBI] 4.12749e-05
PQBP1 [NCBI] 4.06569e-05
HPE2 [NCBI] 3.9043e-05
PC1 [NCBI] 3.9043e-05
TCOF1 [NCBI] 3.80436e-05
cerebrocostomandibular syndrome [NCBI] 3.79251e-05
PFM [NCBI] 3.79251e-05
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 3.79251e-05
HPE3 [NCBI] 3.79251e-05
LRS1 [NCBI] 3.68846e-05
xanthinuria, type i [NCBI] 3.68846e-05
DGI1 [NCBI] 3.68846e-05
TP73L [NCBI] 3.6756e-05
ALPL [NCBI] 3.6362e-05
spondyloepimetaphyseal dysplasia, strudwick type [NCBI] 3.49988e-05
DRRS [NCBI] 3.49988e-05
ED2 [NCBI] 3.49988e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant [NCBI] 3.49988e-05
COL17A1 [NCBI] 3.46004e-05
KFSD [NCBI] 3.41388e-05
crouzon syndrome [NCBI] 3.33262e-05
UMS [NCBI] 3.33262e-05
ichthyosis congenita, harlequin fetus type [NCBI] 3.25564e-05
PALS [NCBI] 3.25564e-05
robinow syndrome, autosomal recessive [NCBI] 3.18252e-05
GABEB [NCBI] 3.11292e-05
weaver syndrome [NCBI] 3.04652e-05
leopard syndrome 1 [NCBI] 2.65255e-05
HFTC [NCBI] 2.65255e-05
HFM [NCBI] 2.61747e-05
PKS [NCBI] 2.55779e-05
MITF [NCBI] 2.52579e-05
COH1 [NCBI] 2.16395e-05
WBS [NCBI] 2.05436e-05
RTS [NCBI] 1.78468e-05
WS1 [NCBI] 1.66537e-05
VWS [NCBI] 1.6429e-05
TCOF [NCBI] 1.53673e-05
HGPS [NCBI] 1.36792e-05
osteogenesis imperfecta, type i [NCBI] 1.22232e-05
SHH [NCBI] 1.20766e-05
SDS [NCBI] 1.13576e-05
NS1 [NCBI] 1.04374e-05
APS1 [NCBI] 9.71584e-06
SMS [NCBI] 9.48775e-06
SPP1 [NCBI] 6.91249e-06
EGF [NCBI] 4.84802e-06
BCNS [NCBI] 4.37767e-06
APC [NCBI] 2.7363e-06
SRS [NCBI] 2.59193e-06
SLOS [NCBI] 2.2652e-06
MFS [NCBI] 1.40825e-06
FA [NCBI] 1.35994e-06
PTH [NCBI] 8.31227e-07
BWS [NCBI] 3.77995e-07




Database Center for Life Science