single median maxillary incisor Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a single, median maxillary incisor, affecting both the primary maxillary incisor and the permanent maxillary incisor. (Human Phenotype Ontology, HP_0006315)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006315
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Genes

7 genes associated with the single median maxillary incisor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
BCOR BCL6 corepressor
EVC Ellis van Creveld protein
GLI2 GLI family zinc finger 2
PTCH1 patched 1
SHH sonic hedgehog
SIX3 SIX homeobox 3