abnormality of incisor morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of morphology of the incisor tooth. (Human Phenotype Ontology, HP_0011063)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011063
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12 genes associated with the abnormality of incisor morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
CCBE1 collagen and calcium binding EGF domains 1
CHSY1 chondroitin sulfate synthase 1
COL11A1 collagen, type XI, alpha 1
CREBBP CREB binding protein
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
VPS13B vacuolar protein sorting 13 homolog B (yeast)
WNT10A wingless-type MMTV integration site family, member 10A